09th week of 2014 patent applcation highlights part 52 |
Patent application number | Title | Published |
20140058416 | Segmented Hernia Patch Frame - A hernia repair prosthesis comprises a segmented frame forming a closed loop where a first segment comprises a helical hollow tube and a second segment comprises a solid strand. Both segments are preferably a metal exhibiting shape memory properties and the two segments are assembled with end portions of the second segment inserted into the lumen at opposed end portions of the first segment with a clearance fit. A prosthetic fabric is attached to the segmented frame. | 2014-02-27 |
20140058417 | VARIABLE DEPTH SURGICAL FIXATION - The invention generally relates to devices for fastening a hernia mesh. The invention provides a surgical fastening device that includes a shaft with a fastener carrier disposed at least partially within the shaft, in which the carrier is configured to accept fasteners of a plurality of different sizes. Different sized fasteners can be preloaded in interchangeable carriers or even mixed together within a carrier in the fastening device. The device can deliver the fasteners to different depths in a patient's tissue. | 2014-02-27 |
20140058418 | METHODS AND DEVICES FOR MANIPULATING AND FASTENING TISSUE - A tissue displacing and fastening device is provided for manipulating and fastening tissue together. The device includes a tissue displacing elements, which displaces tissue. A fold is formed from the displaced tissue and the tissue is fastened together to secure the fold. | 2014-02-27 |
20140058419 | METHOD OF FORMING THROUGH HOLE - This tissue fastening apparatus is a tissue fastener for clamping first biological tissue and second biological tissue so as to be in close contact with each other, including: a first tissue fixation portion, made of an elastic wire wound in a coil, that is locked on the first biological tissue; and a second tissue fixation portion, made of an elastic wire wound in a coil, that is locked on the second biological tissue, the second tissue fixation portion continuing into the first tissue fixation portion, in which when falling off first and second biological tissue necrotized by being clamped between the first tissue fixation portion and the second tissue fixation portion, the tissue fastener moves only from the second tissue fixation portion to the first tissue fixation portion side and falls off. | 2014-02-27 |
20140058420 | IMPLANT, ESPECIALLY FOR THE OCCLUSION OF BIFURCATION ANEURYSMS - The invention relates to an implant ( | 2014-02-27 |
20140058421 | ANCHORING DEVICE FOR ANCHORING A BORING TOOL IN A LUMEN OR VESSEL - An anchoring device ( | 2014-02-27 |
20140058422 | Helically Advancing Constriction Crossing Mechanism And Wire Guide Positioning Method For Performing Percutaneous Vascular Procedures - A vascular procedure includes sliding a constriction crossing mechanism over a wire guide having a tip positioned at a proximal side of a constriction, and rotating a sheath of the mechanism about an axis relative another sheath of the mechanism. The method further includes helically engaging the sheaths, and guiding an intraluminal treatment device into or past the vascular constriction. The mechanism includes a first sheath and a second sheath, and a tip coupled with the first sheath. The mechanism further includes a helical coupling between the first and second sheaths, which is configured to convert a torque on one of the sheaths to an axial force on the other of the sheaths for crossing a vascular constriction with the tip. An anchoring mechanism coupled with one of the sheaths includes a deployed state resisting displacement of the second sheath within a vascular structure of a patient. | 2014-02-27 |
20140058423 | ATHERECTOMY APPARATUS, SYSTEMS AND METHODS - Described here are devices and methods for performing atherectomies. Generally, the atherectomy devices may comprise a handle, a cutter assembly, and a catheter or catheter assembly therebetween. The cutter assembly may include a cutter housing and a cutter comprising a first cutting element and a second cutting element, each of which may be rotated relative to the atherectomy device to cut occlusive material. | 2014-02-27 |
20140058424 | NOVEL MICROFABRICATED INSTRUMENTS AND METHODS TO TREAT RECURRENT CORNEAL EROSIONS - In one embodiment, the present invention provides a device and method for treating recurrent corneal erosion. In one embodiment, the method includes the steps of contacting an epithelium layer of a cornea with an array of glass micro-rods including a plurality of sharp features having a length that penetrates a Bowman's layer of the eye, wherein the plurality of sharp features of the array of glass micro-rods produces a plurality of punctures in the Bowman's layer of the eye that are of micro-scale or less. In another embodiment, the present invention provides a method and device for drug delivery. In one embodiment, the device includes an array of glass micro-rods, wherein at least one glass micro-rod of the array of glass micro-rods includes a sharp feature opposite a base of the array of glass micro-rods, wherein the sharp feature includes a treated surface for delivering a chemical compound to the eye. | 2014-02-27 |
20140058425 | MANUALLY OPERATED SURGICAL DEVICES WITH OPERATIVE PORTIONS FORMED OF A SEE-THROUGH MATERIAL - The disclosure is directed to a manually operated surgical device comprises a proximal control means portion for manually operating the device; and a see-through distal operative means portion operably coupled to the proximal control means, wherein the distal operative means portion is formed of a material that is different than the material forming the proximal control means portion. | 2014-02-27 |
20140058426 | METHOD OF AND APPARATUS FOR POSITIONING AND MAINTAINING THE POSITION OF ENDOSCOPIC INSTRUMENTS - The present invention provides an apparatus for, and a method of, accurate positioning of endoscopic instruments. Accurate positioning of the instruments is accomplished through the inclusion of a steering ability within the device. After the endoscopic instrument is properly positioned, the present invention may use rapid exchange technology, soft locks, and mechanical locks to maintain the position of the endoscopic instrument. Rapid exchange technology is used to minimize displacement forces present on the guidewire or catheters. Soft locks and mechanical locks resist movements caused by displacement forces. | 2014-02-27 |
20140058427 | ULTRASONIC SURGICAL INSTRUMENT BLADES - An ultrasonic surgical instrument including an ultrasonically actuated blade or end effector having a treatment portion. The blade can define a central axis and at least one axis which is transverse to the central axis, wherein the transverse axis can lie within a plane which is perpendicular, or normal, to the longitudinal axis and can define a cross-section of the treatment portion. Such a cross-section can include a central portion and a step extending from the central portion, wherein the central portion can comprise a width, and wherein the step can comprise a cutting edge. In at least one embodiment, the cutting edge can be defined by first and second surfaces which define an angle therebetween. In various embodiments, the position of the cutting edge and/or the angle between the cutting edge surfaces can be selected in order to balance the blade with respect to the transverse axis. | 2014-02-27 |
20140058428 | TWIST-TO-CHARGE MECHANISM OF LANCING DEVICE - A lancing device includes a housing, a lancet carrier translational within the housing, a drive spring for propelling the lancet carrier through a translational lancing stroke, and a charging mechanism. The charging mechanism includes a first cam member that is rotatable relative to the housing, a second cam member that abuts the first cam member, is coupled to the lancet carrier, and is restricted from rotation relative to the housing, and a rotatable handle co-rotationally attached to the first cam member. Rotation of the handle rotates the first cam member with it, causing the first cam member to rotate against the second cam member, which in response traverses axially because it is restricted from rotation, thereby retracting the lancet carrier to a retracted or charged state. | 2014-02-27 |
20140058429 | COLLAPSIBLE SHEATH AND TAPERED DILATOR FOR TISSUE PUNCTURE ACCESS - A tissue puncture access assembly that includes a sheath and a dilator. The sheath is operable between an expanded position with a first maximum outer diameter, and a collapsed position with a second maximum outer diameter that is less than the first maximum outer diameter. The dilator is insertable through the sheath and has a leading end positionable distal of a distal end of the sheath. The sheath is operated into the collapsed position prior to and during insertion with the dilator into a tissue puncture. The sheath is operated into the expanded position once positioned in the tissue puncture. | 2014-02-27 |
20140058430 | INTRANASAL BONE REMODELING DEVICES AND THEIR PLACE IN MINIMALLY INVASIVE SINUS PROCEDURES - A method is provided for accessing and treating at least one of a maxillary sinusitis, sphenoid sinusitis and frontal sinusitis. A perforation is created in an uncinate via an anterior keyhole. A position of an MSO is verified using a probe. The probe is used to verify dimensions of the MSO. A verification is made that an anteroposterior length of the ostium is sufficient. A targeted medial displacement of a medial wall of the maxillary sinus and uncinate is made using an uncinate medializing device. | 2014-02-27 |
20140058431 | CORING TOOL - The present invention related to a coring tool for preparing a core or opening through tissue and methods of use thereof. In one embodiment, the present invention include a coring tool including: (a) a frame having proximal and distal directions; (b) an operator interface element mounted to the frame and movable between a rest position and an actuated position; (c) a coring head having at least one cutting blade, the coring head being mounted to the frame for movement in the proximal and distal directions; and (d) a actuation mechanism connected between the coring head and the operator interface element, the actuation mechanism including a selector element having first and second positions, the actuation mechanism being arranged to move the coring head distally responsive to movement of the interface element from the rest position toward the actuated position when the selector element is in the first position, and to move the coring head proximally responsive to movement of the interface element from the rest position toward the actuated position when the selector element is in the second position. | 2014-02-27 |
20140058432 | INSTRUMENTS AND METHODS FOR FORMING A CAVITY - A cavity creating device having a cavity creating axis is introduced through a percutaneous access path into a cancellous bone volume, e.g., within a vertebral body. The cavity creating device is manipulated to form a cavity in the cancellous bone volume. The manipulation includes deflecting the cavity creating device along the cavity creating axis relative to the axis of the access path. A material, such as bone cement, can be conveyed into the cavity. | 2014-02-27 |
20140058433 | BRONCHIAL ISOLATION DEVICES FOR PLACEMENT IN SHORT LUMENS - Methods and devices are adapted for regulating fluid flow to and from a region of a patient's lung, such as to achieve a desired fluid flow dynamic to a lung region during respiration and/or to induce collapse in one or more lung regions. Pursuant to an exemplary procedure, an identified region of the lung is targeted for treatment. The targeted lung region is then bronchially isolated to regulate airflow into and/or out of the targeted lung region through one or more bronchial passageways that feed air to the targeted lung region. | 2014-02-27 |
20140058434 | RELEASABLE DEVICE SYSTEM - A medical implant deployment system for placing an implant at a preselected site within a vessel, duct or body lumen of a mammal. The reusable deployment system includes a mechanical coupling assembly at the distal end of a positioning member, having a first configuration in which the coupling assembly distal end is insertable or removable from the implant proximal end and a second configuration where the coupling assembly distal end is interlockingly engaged with the implant proximal end. Once the implant is properly positioned the coupling assembly is actuated, thereby releasing the implant at a desired position within the body. | 2014-02-27 |
20140058435 | IMPLANT DELIVERY AND RELEASE SYSTEM - A medical implant deployment system for placing an implant at a preselected site within a vessel, duct or body lumen of a mammal comprising a reloadable deployment system includes a mechanical coupling assembly at the distal end of a delivery member, having an extended configuration in which the coupling assembly is adapted to receive or release the implant proximal end and a retracted configuration where the coupling assembly distal end is interlockingly engaged with the implant proximal end. Once the implant is properly positioned the coupling assembly is actuated, thereby releasing the implant at a desired position within the body. | 2014-02-27 |
20140058436 | BLOOD FLOW DISRUPTION DEVICES AND METHODS FOR THE TREATMENT OF VASCULAR DEFECTS - A blood flow disruption device for embolizing blood flowing into a vascular defect between a proximal vascular segment and a distal vascular segment, wherein the device includes a porous inner flow disruption element configured to extend through the defect between the proximal vascular segment and the distal vascular segment, whereby a first portion of the blood flowing into the inner flow disruption element from the proximal vascular segment is directed to flow into the defect and a second portion of the blood flowing into the inner flow disruption element is directed to flow into the distal vascular segment. A porous outer flow disruption element coaxially surrounds the inner flow disruption element and is radially expansible from a collapsed state to an expanded state. The outer flow disruption element, in its expanded state, promotes sufficient hemostasis of the first portion of the blood within the defect to embolize the defect. | 2014-02-27 |
20140058437 | Removable Embolus Blood Clot Filter - A removable blood clot filter includes a number of locator members and anchor members disposed radially and extending angularly downward from a hub. The locator members include a number of linear portions having distinct axes configured to place a tip portion approximately parallel to the walls of a blood vessel when implanted and to apply sufficient force to the vessel walls to position the filter near the vessel centerline. The anchor members each include a hook configured to penetrate the vessel wall to prevent longitudinal movement due to blood flow. The hooks may have a cross section sized to allow for a larger radius of curvature under strain so that the filter can be removed without damaging the vessel wall. | 2014-02-27 |
20140058438 | CARRIER TUBES FOR CLOSURE DEVICES - A deployment device having a carrier tube, for bringing a sealing plug into position within a puncture tract or incision and deploying the sealing plug within the incision or puncture tract, towards the outer surface of a tissue puncture, is provided. The carrier tube is designed to facilitate easier deployment and improved compaction of the sealing plug, the sealing plug often made of collagen. The carrier tube is adapted to prevent the premature hydration of the sealing plug, where premature hydration of the sealing plug may result in difficulty in deploying the sealing plug. The carrier tube is designed to facilitate easier loading of puncture tract closing elements into the distal end of the carrier tube. | 2014-02-27 |
20140058439 | SEALING MECHANISM FOR CLOSURE DEVICES - A deployment device for bringing a sealing plug into position within a puncture tract or incision, and bringing an anchor into position adjacent a tissue puncture, is provided. The deployment device is designed to facilitate easier positioning of the sealing plug, wherein a separate tamping tool is not required. The sealing plug is held in place on the shaft of the anchor by a structure, for example, a knob or boss. The anchor, anchor shaft, and sealing plug may be made of various biocompatible resorbable materials such that the anchor may resorb very quickly, leaving the tissue or artery lumen clear, and the sealing plug may resorb more slowly, to assist in maintaining hemostasis. The deployment device may include a bypass device which maintains the anchor in either an extended or bent configuration. Further, the anchor may include at least one rib, to provide support to the anchor. | 2014-02-27 |
20140058440 | BALLOON BAILOUT AND BIOADHESIVE DELIVERY DEVICE FOR SUTURE BASED CLOSURE AND METHODS - A vascular closure assembly is configured to seal a vascular puncture in a vessel. The vascular closure assembly includes a balloon location device and a sealant delivery device. The balloon location device includes an inflation tube and an inflatable balloon positioned at a distal end of the inflation tube and operable, when inflated, between a first position blocking blood flow through the vessel and a second position sealing the puncture from within the vessel. The sealant delivery device includes a sealant delivery tube having a first lumen sized to advance over the inflation tube to the puncture, and a second lumen configured to deliver a volume of sealant to the puncture. The first lumen may include a rapid exchange feature. | 2014-02-27 |
20140058441 | BIOADHESIVE MIXING AND DELIVERY DEVICE AND METHODS - A tissue puncture closure device includes a delivery member, a handle assembly, and a sealant cartridge. The delivery member includes a sealant lumen and is insertable into a tissue puncture. The handle assembly is mounted to a proximal end of the delivery member and includes a cartridge chamber and a plunger member. The sealant cartridge is insertable into the cartridge chamber. The sealant cartridge has at least first and second sealant chambers carrying at least first and second sealant components, respectively. Operation of the handle assembly ejects the first and second sealant components into the sealant lumen for delivery to the tissue puncture. | 2014-02-27 |
20140058442 | SEALANT STORAGE, PREPARATION, AND DELIVERY SYSTEMS AND RELATED METHODS - A bioadhesive sealant storage and preparation system may comprise a plurality of containers and an adapter. The plurality of containers may comprise a first container having a first bioadhesive sealant component therein, and a second container having a second bioadhesive sealant component therein. The adapter may comprise a manifold comprising a plurality of channels formed therein, an inlet region sized and configured to receive the plurality of containers and facilitate fluid communication between each container of the plurality of containers and a respective channel of the plurality of channels, and an outlet region sized and configured to receive a syringe and provide fluid communication between the syringe and the plurality of channels. | 2014-02-27 |
20140058443 | VASCULAR WOUND CLOSURE DEVICE AND METHOD - A method and apparatus for closing a vascular wound includes an apparatus that can be threaded over a guidewire into place at or adjacent the wound. The apparatus includes a chamber that encloses a hemostatic material therein. When the apparatus is positioned adjacent the wound as desired, the hemostatic material is deployed from the chamber. A blocking member distal of the hemostatic material functions as a barrier to prevent the hemostatic material from entering the wound. Blood contacts the hemostatic material, and blood clotting preferably is facilitated by a hemostatic agent within the material. Thus, the vascular puncture wound is sealed by blood clot formation. | 2014-02-27 |
20140058444 | Devices for Securely Closing Tissue Openings with Minimized Scarring - Devices, tools, systems, kits and methods for closing a tissue opening non-invasively are presented. The devices include a tissue closure device that reliably induces eversion of tissue edges that define a tissue opening. The devices may be used in combination with an applicator tool to provide easy and uniform apposition of the tissue closure devices across the tissue opening. Further embodiments provide for releasable locking of the tissue closure devices, allowing for drainage of wound edema and/or treatment of infection, without removal and reapplication of the devices. Still further embodiments allow for the passing of moisture or other substances that may collect under a tissue closure device. | 2014-02-27 |
20140058445 | HIGH TENSION SUTURE ANCHOR - The present invention describes a bio-medically compatible gripping device capable of radial collapse in accordance with the shrinkage of a nylon or other polymeric material cored surgical cable undergoing tension while maintaining a firm grip throughout the process. It provides a gripping device capable of maintaining a grip on the outer surface of a slippery delicate cable, the grip being approximately uniform along both the length and circumference of the cable. The present invention also provides a gripping device capable of maintaining a grip, yet not damage, a delicate cable under high tension for a period of time adequate for as the healing process to occur. | 2014-02-27 |
20140058446 | SPINAL IMPLANT SYSTEM - A spinal implant system and method of assembling the system. The system includes an implant, an integral holder/connector to grasp the implant and to connect to a plate before the assembly is inserted into a patient. | 2014-02-27 |
20140058447 | Spinal Facet Implants with Mating Articulating Bearing Surface and Methods of Use - Superior and/or inferior facets of one or more facet joints may be replaced by superior and/or inferior facet joint prostheses. In one embodiment, a kit of superior or inferior prostheses is provided, in which the prostheses have at least two dimensions that vary among members of the kit independently of each other. Each prosthesis may have a bone engaging surface having a surface that is polyaxially rotatable against a corresponding resection of a vertebra. Each prosthesis may also have an articulating surface shaped such that, after attachment to the spine, the replaced or partially replaced facet joints provide a larger medial-lateral range of motion when the spine is flexed than when the spine is extended. Crosslinks may be used to connect left and right prosthesis together in such a manner that they are stabilized in a position in which they are seated directly against the vertebra. | 2014-02-27 |
20140058448 | Minimally Invasive Spine Restoration Systems, Devices, Methods and Kits - The invention discloses methods, devices, systems and kits for repairing, replacing and/or augmenting natural facet joint surfaces and/or facet capsules. An implantable facet joint device of one embodiment comprises a cephalad facet joint element and a caudal facet joint element. The cephalad facet joint element includes a member adapted to engage a first vertebra, and an artificial cephalad bearing member. The caudal facet joint element includes a connector adapted for fixation to a second vertebra at a fixation point and an artificial caudal bearing member adapted to engage the cephalad bearing member. The artificial caudal bearing member is adapted for a location lateral to the fixation point. In another embodiment, an implantable facet joint device comprises a cephalad crossbar adapted to extend mediolaterally relative to a spine of a patient, the crossbar having opposite first and second ends, a connector element adapted to connect the crossbar to a first vertebra, a first artificial cephalad bearing member adapted for connection to the first end of the crossbar and adapted to engage a first caudal facet joint element connected to a second vertebra, and a second artificial cephalad bearing member adapted for connection to the second end of the crossbar and adapted to engage a second caudal facet joint element connected to the second vertebra. | 2014-02-27 |
20140058449 | Linked Bilateral Spinal Facet Implants and Methods of Use - Superior and/or inferior facets of one or more facet joints may be replaced by superior and/or inferior facet joint prostheses. In one embodiment, a kit of superior or inferior prostheses is provided, in which the prostheses have at least two dimensions that vary among members of the kit independently of each other. Each prosthesis may have a bone engaging surface having a surface that is polyaxially rotatable against a corresponding resection of a vertebra. Each prosthesis may also have an articulating surface shaped such that, after attachment to the spine, the replaced or partially replaced facet joints provide a larger medial-lateral range of motion when the spine is flexed than when the spine is extended. Crosslinks may be used to connect left and right prosthesis together in such a manner that they are stabilized in a position in which they are seated directly against the vertebra. | 2014-02-27 |
20140058450 | SPINAL CORRECTION SYSTEM AND METHOD - A spinal construct comprises a first member defining a longitudinal axis and extending between a first end and a second end being offset relative to the longitudinal axis. A second member defines a longitudinal axis and extends between a first end and a second end being offset relative to the longitudinal axis of the second member. The second ends are connected to define an axis of rotation such that the members are relatively rotatable about the second ends and the axis of rotation is offset relative to the longitudinal axes. Systems and methods are disclosed. | 2014-02-27 |
20140058451 | Polyaxial Screw - The present invention generally is directed toward a spinal fixation system whereby a coupling element allows the physician to selectively lock or unlock either the connection between the coupling element and a fastener, such as to allow for repositioning of the coupling element, or the connection between the coupling element and an elongate rod. The locking or unlocking of these connections may be made independently and as desired by the physician. | 2014-02-27 |
20140058452 | Polyaxial Screw - The present invention generally is directed toward a spinal fixation system whereby a coupling element allows the physician to selectively lock or unlock either the connection between the coupling element and a fastener, such as to allow for repositioning of the coupling element, or the connection between the coupling element and an elongate rod. The locking or unlocking of these connections may be made independently and as desired by the physician. | 2014-02-27 |
20140058453 | Prosthetic Ligament Having a Helical Bone Fastener - An intervertebral connection system wherein the bone anchor has a helical configuration. Also included is a method of installing a bone fastening connection system, comprising the steps of:
| 2014-02-27 |
20140058454 | Multi-Axial Connection System - A system and method for a multi-axial connection of an apparatus to bone. The system may include a fastener inserted into a body and a head of the fastener held within a chamber of the body through a combination of a retention ring, a pressure cap, a rod, and a compression element. The compression element applies force to the rod which, in turn, pushed on the pressure cap. The force on the pressure cap urges it against the head of the fastener and pushed it against the retention ring. The force on the retention ring causes it to expand to the walls of the chamber. Once the ring can no longer expand within the chamber, the head of the fastener is wedged between the retention ring and the pressure cap. | 2014-02-27 |
20140058455 | Bone Fixation System - A bone fixation system has a bone implant with an implant body. The implant body defines an upper surface, a bone-facing surface spaced from the upper surface along a transverse direction, and at least one aperture defined by an inner wall. A bone fixation element is configured for insertion at least partially through the aperture. The bone fixation element defines a proximal end and a distal end spaced from the proximal end along a central axis. The bone fixation element has a head and a shaft that extends relative to the head toward the distal end. The head defines a first ridge, a second ridge spaced from the first ridge, and a groove disposed between the first and second ridges. The groove can receive at least a portion of the inner wall to couple the bone fixation element to the bone implant. | 2014-02-27 |
20140058456 | Distal Radius Fracture Fixation Plate with Ulnar Buttress - A distal volar fixation plate includes a body portion and a head portion angled upwards relative to the body portion. The head portion includes a lower surface, a central portion, a radial side and an ulnar side. The head portion defines a buttress portion extends greater distally on the ulnar side than on the radial side to support the volar lip of the lunate fossa. | 2014-02-27 |
20140058457 | ANCHOR-IN-ANCHOR SYSTEM - An anchor-in-anchor fixation system is provided for securing underlying structure, such as bone. The fixation system includes a linkage that defines first and second bores, a first bone anchor having a shaft for fixation to underlying bone, and a head that is configured to attach to the linkage in the first bore, and a second bone anchor having a shaft for fixation to underlying bone and a head that is configured to attach to the linkage in the second bore. | 2014-02-27 |
20140058458 | POLYAXIAL SCREW ASSEMBLY - A polyaxial screw assembly includes a pedicle screw, a coupling, an insert, and a housing. The pedicle screw includes a shank having a helical thread formed thereon and a head at one end. The coupling is positioned on top the pedicle screw and releasably engages portions of the head. The coupling and pedicle screw are positioned within a distal portion of the housing. The pedicle screw is slid through an opening in the insert and the insert is thread into the distal portion of the housing to retain the coupling and the pedicle screw within the housing. The pedicle screw is rotatable and pivotable relative to the housing. Compressing the coupling within the housing locks the pedicle screw in a desired orientation. | 2014-02-27 |
20140058459 | Pedicle Screw Fixation System and Method for Use of Same - A pedicle screw fixation system and method for use of the same are disclosed. In one embodiment, a tulip is provided for holding a head of a pedicle screw substantially along a longitudinal axis. The tulip includes opposing first and second U-shaped receiving slots aligned along a transverse axis. A rod is received by the opposing first and second U-shaped receiving slots. A coupling collar includes a plurality of resilient fingers circumferentially disposed therearound such that a snap fit engagement with the head of the pedicle screw formed. The coupling collar includes a first deformable face operable for contact with the rod. A set screw is for adapted for driving engagement through the tulip along the longitudinal axis such that a second deformable face is positioned for contact with the rod. The first and second deformable faces conform to the shape of the rod in response to forceful engagement therewith. | 2014-02-27 |
20140058460 | Orthopedic fastener device - An orthopedic structure includes a method for making a threaded fastener with thread geometry and leading edge geometry which provides greater precision during installation. Specifically, thread pitch and tooth profiles are independently variable. A leading portion of the fastener advances bone shards forward of the forward of the fastener to reduce insertion torque and prevent the shards from residing in the upstream tooth profile for better retention. | 2014-02-27 |
20140058461 | Fenestrated Bone Screw - Improved bone screws are provided. The bone screws comprise a head portion that is connected to a shaft portion. The shaft portion can comprise one or more fenestrations that extend along a length of the screw. The fenestrations can be straight, or they can include angled bends and arcuate curves. At least a portion of the bone screws can be shot-peened or cold-worked in order to increase the strength of the bone screws to allow for use in, among other regions, the cervical region of the spine. | 2014-02-27 |
20140058462 | HAMMER TOE IMPLANT WITH EXPANSION PORTION FOR RETROGRADE APPROACH - An implant for fusing adjacent bones is disclosed. The implant includes an elongate threaded member and a flexible portion extending from the elongate threaded member. The flexible portion includes a plurality of prongs configured to be reversibly compressed toward an axis defined by the elongate threaded member. | 2014-02-27 |
20140058463 | BONE ANCHORING DEVICE - A bone anchoring device includes a receiving part for receiving a rod, the receiving part has a first bore coaxial with a longitudinal axis and a second bore, and an anchoring element having a first end for insertion into the bone and a second end positionable within a second bore, the anchoring element being movable relative to the receiving part in limited angular range about the longitudinal axis, the angles lying in a single plane. The bone anchoring device further includes a fixation element cooperating with the receiving part to lock the anchoring element relative to the receiving part. The anchoring element is pivotable relative to the receiving part around one rotational axis transverse to the longitudinal axis. | 2014-02-27 |
20140058464 | BI-PLANAR PERSUADER - The present disclosure relates generally to surgical instruments for spinal surgery. More specifically, the present disclosure relates to a bi-planar rod persuader for urging a spinal rod into a screw, and methods regarding the same. The bi-planar rod persuader may include an implant holder, which may also include a holding sleeve. A securing foot may be attached to the distal end of the holding sleeve, and the holding sleeve may also include a threaded opening at the proximal end for receiving a stem that drives the securing foot between a first position and second position. The implant holder may also include a threaded part to engage a reduction knob. A handle assembly may also be provided, which may include two pivotally attached arms. A rod hook may be connected to one of the arms and a guide attached to the other of the arms. | 2014-02-27 |
20140058465 | APPARATUS FOR SECURING A SPINAL ROD SYSTEM - The present invention includes an apparatus for securing a spinal rod with an anchoring device, the apparatus including a tubular body defining a longitudinal axis from a proximal end to a distal end; a connecting element positioned within the tubular body and along the longitudinal axis, the connecting element engaged by a first internal shaft and a second internal shaft, the tubular body, first internal shaft and second internal shaft coaxial with one another; the first internal shaft rotatably engages the connecting element such that rotation of the first internal shaft results in axial translation of the connecting element; and the second internal shaft engages the connecting element such that rotation of the second internal shaft results in rotation of the connecting element. | 2014-02-27 |
20140058466 | SURGICAL GUIDING TOOLS AND SYSTEMS AND METHODS OF MANUFACTURING SURGICAL GUIDING TOOLS - The present application relates to surgical guiding tools that may be used for guiding a surgical instrument during bone surgery. A surgical guiding tool may include a body including one or more clamps configured to attach the surgical guiding tool to one or more portions of the bone, wherein a first clamp of the one or more clamps includes a snap-fit portion including a flexible structure for increasing a clamping force of the first clamp and allowing ease of removal of the surgical guiding tool from the bone. The surgical guiding tool may further include at least one aperture for guiding a surgical instrument. The present application further provides methods for manufacturing surgical guiding tools and uses of the tools for placement onto a bone. | 2014-02-27 |
20140058467 | IMPLANTABLE MEDICAL DEVICE WITH CONTROL OF NEURAL STIMULATION BASED ON BATTERY STATUS - An implantable medical device is powered by a battery to deliver one or more therapies including at least one non-life-sustaining therapy such as neural stimulation for enhancing quality of life of a patient. When the battery approaches its end of life, the implantable medical device reduces power consumption of the neural stimulation (e.g., intensity of the neural stimulation) for extending the remaining battery life while maintaining a certain amount of therapeutic benefits for the patient. In one embodiment, the intensity of the neural stimulation is reduced in a tiered manner. In one embodiment in which the implantable medical device also delivers at least one life-sustaining cardiac stimulation therapy, the neural stimulation is disabled or adjusted to reduce its power consumption (e.g., intensity) while the intensity of the cardiac stimulation therapy is maintained when the battery is near its end of life. | 2014-02-27 |
20140058468 | USE CASE-BASED SERVICES - An apparatus comprises an external device for communication with an implantable device. The external device includes a communication circuit configured to receive a communication signal from at least a third device separate from the external device and the implantable device, a locating circuit configured to determine a location of the external device using the received communication signal, a port configured to receive user identity information into the external device, and a control circuit electrically coupled to the communication circuit, the locating circuit, and the port. The control circuit is configured to allow user access to an implantable device feature according to the determined location and received user identity information. | 2014-02-27 |
20140058469 | PULSE DETECTION USING PATIENT PHYSIOLOGICAL SIGNALS - The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates optical characteristics of light transmitted into a patient to ascertain physiological signals, such as pulsatile changes in general blood volume proximate a light detector module. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided. | 2014-02-27 |
20140058470 | MULTI-STAGE ATRIAL CARDIOVERSION THERAPY LEADS - Devices and methods of use for treating atrial arrhythmias. A single-pass lead includes a body portion having at least two electrodes configured to be positioned within or adjacent a right atrium of a heart of a patient, and a distal portion having at least two electrodes configured to be positioned within a blood vessel proximate the left atrium. The lead is configured to operated by an implantable therapy generator programmed to deliver a multi-stage therapy by activating various combinations of at least one electrode of the body portion of the lead and at least one electrode of the distal portion of the lead. | 2014-02-27 |
20140058471 | MEASURING AUTONOMIC TONE USING ATRIOVENTRICULAR DELAY - An autonomic status indicator representative of a sympathetic/parasympathetic balance of a subject can use atrioventricular (AV) delays measured during recovery from (or in response to) elevated atrial pacing while the subject is at rest. | 2014-02-27 |
20140058472 | BIVENTRICULAR-TRIGGERED PACING IN THE CONTEXT OF MULTI-SITE LEFT VENTRICULAR PACING - Biventricular-triggered pacing is a pacing mode that can employ in cardiac resynchronization pacing at elevated heart rates. Described herein are methods and devices for implementing biventricular pacing in the context of multi-site left ventricular pacing. | 2014-02-27 |
20140058473 | Uterine Electrical Stimulation System and Method - Some embodiments of the invention provide a system and method for treating insufficient uterine contractions after labor and delivery. The system includes a control module and a current source controlled by the control module to produce stimulating current at a frequency greater than or equal to about 5.0 Hertz. The system also includes one or more stimulation electrodes to provide the stimulating current to the patient in order for the patient to produce tonic uterine contractions. | 2014-02-27 |
20140058474 | DEVICES AND METHODS FOR STIMULATING NERVES - A device for stimulating nerves adjacent the vagina includes a nerve stimulating element coupled to a body. The nerve stimulating element is positioned to stimulate the vesical, Frankenhauser's and/or inferior hypogastric plexuses. The device may reside in the vaginal fornices. | 2014-02-27 |
20140058475 | METHOD FOR PROGRAMMING IMPLANTABLE DEVICE - A programming system for selecting an electrode configuration for use in a medical electrical stimulator coupled to an electrode array. A programmer is configured for providing a set of electrode configurations for the electrode array, automatically testing a first portion of the set of electrode configurations in a first order, allowing the selection of one or more of the tested electrode configurations, determining whether a suitable number of electrode configurations from among the first portion have been selected within a predefined interval, and automatically testing a second portion of the set of electrode configurations in a second order if the suitable number of electrode configurations from among the first portion are not selected within the predefined interval. The programmer may further allow the selection of the tested electrode configurations, and adjusting parameters during the testing, wherein the adjusting is controllably shared in parallel between a clinician and a patient. | 2014-02-27 |
20140058476 | APPARATUS AND METHODS FOR REHABILITATING A MUSCLE AND ASSESSING PROGRESS OF REHABILITATION - Apparatus and methods for rehabilitating a muscle are provided including one or more electrodes configured to be positioned in or adjacent to tissue, one or more sensors configured to sense muscle contraction and to generate a sensor signal based on the muscle contraction, and a pulse generator operatively coupled to the one or more electrodes, e.g., via a lead, and having a controller configured to receive the sensor signal and to adjust the stimulation frequency based on the sensor signal to cause the muscle to contract where muscle contraction is smooth and continuous. | 2014-02-27 |
20140058477 | Synergistic Muscle Activation Device - Systems and methods of use for guiding the flow of energy through a subject to stimulate tissue. | 2014-02-27 |
20140058478 | Reduction of Transient Sounds in Hearing Implants - A method is described for generating electrode stimulation signals for electrode contacts in a cochlear implant electrode array. An input audio signal is processed to generate band pass channel signals that each represent an associated band of audio frequencies. A channel envelope is extracted from each channel signal. The input audio signal and the channel envelopes are processed to produce transient reduced envelopes based on: i. determining for each channel envelope a normalized channel-specific transient indicator characterizing transient noise present in the channel signal, ii. determining a combined transient indicator as a function of the channel-specific transient indicators, and iii. applying a channel-specific gain to the channel envelopes as a function of the combined transient indicator to produce the transient reduced envelopes. The transient reduced envelopes are then used to generate electrode stimulation signals to the electrode contacts. | 2014-02-27 |
20140058479 | Minimizing Interference Between Charging and Telemetry Coils in an Implantable Medical Device - An improved implantable pulse generator (IPG) containing improved telemetry circuitry is disclosed. The IPG includes charging and telemetry coils within the IPG case, which increases their mutual inductance and potential to interfere with each other; particularly problematic is interference to the telemetry coil caused by the charging coil. To combat this, improved telemetry circuitry includes decoupling circuitry for decoupling the charging coil during periods of telemetry between the IPG and an external controller. Such decoupling circuitry can comprise use of pre-existing LSK circuitry during telemetry, or new discrete circuitry dedicated to decoupling. The decoupling circuitry is designed to prevent or at least reduce induced current flowing through the charging coil during data telemetry. The decoupling circuitry can be controlled by the microcontroller in the IPG, or can automatically decouple the charging coil at appropriate times to mitigate an induced current without instruction from the microcontroller. | 2014-02-27 |
20140058480 | REMOTE CONTROL OF POWER OR POLARITY SELECTION FOR A NEURAL STIMULATOR - A system, including: an implantable neural stimulator including electrodes, at least one antenna and an electrode interface; a radio-frequency (RF) pulse generator module comprising an antenna module configured to send an input signal to the antenna in the implantable neural stimulator through electrical radiative coupling, the input signal containing electrical energy and polarity assignment information that designates polarity assignments of the electrodes in the implantable neural stimulator; and wherein the implantable neural stimulator is configured to: control the electrode interface such that the electrodes have the polarity assignments designated by the polarity assignment information, create one or more electrical pulses suitable for modulation of neural tissue using the electrical energy contained in the input signal, and supply the electrical pulses to the electrodes through the electrode interface such that the electrodes apply the electrical pulses to the neural tissue with the polarity assignments designated by the polarity assignment information. | 2014-02-27 |
20140058481 | NEURAL STIMULATOR SYSTEM - An implantable neural stimulator method for modulating excitable tissue in a patient including: implanting a neural stimulator within the body of the patient such that one or more electrodes of the neural stimulator are positioned at a target site adjacent to or near excitable tissue; generating an input signal with a controller module located outside of, and spaced away from, the patient's body; transmitting the input signal to the neural stimulator through electrical radiative coupling; converting the input signal to electrical pulses within the neural stimulator; and applying the electrical pulses to the excitable tissue sufficient to modulate said excitable tissue. | 2014-02-27 |
20140058482 | IMPLANTABLE ELECTRICAL STIMULATION SYSTEMS WITH SHIELDED CONTROL MODULE AND METHODS FOR MAKING AND USING - An implantable control module for an electrical stimulation system includes a header coupled a sealed body. The header includes at least one connector assembly. The control module also includes a conductive shield disposed over at least a portion of the connector assembly or connector assemblies of the header. The conductive shield is provided to hinder generation of current in the header or in a portion of a lead received in the header in response to application of an external radiofrequency (RF) or magnetic field. A similar shield can also be used to shield a connector assembly disposed on the end of a lead extension or any other component of the electrical stimulation system. | 2014-02-27 |
20140058483 | STIMULI GENERATING METHODS, DEVICES AND CONTROL SYSTEMS TO INDUCE VISUAL EVOKED POTENTIALS USING IMPERCEPTIBLE FLICKERING MULTI-COLOR LIGHTS - Visual or photic stimuli generating methods, devices and control systems for inducing steady-state visual evoked potential (SSVEP) from human viewers without causing discomfort to the viewers or distorting the embedding images are disclosed. The control system includes a stimuli-generating device and an electroencephalography (EEG) sensing device. The stimuli-generating device includes a first and a second light source. The first light source generates a flickering light with a first wavelength while a second light source generates another flickering light with one or more wavelength(s) differ from that of the first one. Together, the light sources generate visual/photic stimuli flickering above their critical flicker fusion threshold while maintaining the colorfulness and hue of the embedding images. At least one electrode of the EEG sensing device is connected to each viewer, configured to receive and analyze his/her EEG signals in order to detect and determine his/her responses to the stimuli. | 2014-02-27 |
20140058484 | SYSTEM AND METHOD FOR DETERMINING AND CONTROLLING CORE BODY TEMPERATURE - Systems and methods for accurate temperature modification of a patient, or selected regions thereof, including inducing hypothermia. The temperature modification is accomplished using an in-dwelling heat exchange catheter within which a fluid heat exchange medium circulates. A heat exchange cassette attached to the circulatory flow lines of the catheter, the heat exchange cassette being sized to engage a cavity within a control unit. A temperature measurement scheme for obtaining body core temperature is provided, including methods of obtaining and analyzing temperature data to provide feedback to the control unit for use in controlling the heating and cooling of the heat exchange medium so as to heat or cool a patient to a desired target temperature. | 2014-02-27 |
20140058485 | PATIENT COMFORT APPARATUS AND SYSTEM - An apparatus, a system, and a method for thermally comforting a patient include pneumatic, convective device providing thermal treatment for persons or animals, which is adapted for use in combination with a clinical garment such as a hospital gown, robe, bib, and other equivalents. The pneumatic convective device provides convective warming focused or directed primarily on the thorax or body core. The pneumatic convective device includes at least one inlet for being accessed through a clinical garment, a region in distribution with the inlet for distributing a stream of pressurized, thermally treated air, and a permeable member for emitting pressurized, thermally treated air from the distribution region. | 2014-02-27 |
20140058486 | SECURABLE ICE PACK DEVICE - An ice pack device that may be secured to an appendage to be treated. The ice pack device may include a body portion that includes an ice pack compartment. The ice pack compartment may secure ice, refrigerant gel, or liquids. Extending from the body portion may be at least one first strap and at least one second strap. The ice pack device may be secured to the appendage by wrapping the straps around the appendage and releasably connecting them. | 2014-02-27 |
20140058487 | SYSTEMS AND METHODS FOR IMPROVING RF COMPATIBILITY OF ELECTRICAL STIMULATION LEADS - An implantable lead for stimulating patient tissue includes a lead body. A jacket is disposed over at least a portion of a length of the lead body. The jacket has an outer surface and an opposing inner surface. At least a portion of the outer surface of the jacket forms at least a portion of an outer surface of the lead. At least a portion of the inner surface of the jacket is open to the lead body. The jacket defines apertures each extending completely through the jacket. Electrodes are disposed along a distal end of the lead body. Terminals are disposed along a proximal end of the lead body. Conductors electrically couple the electrodes to the terminals. Conductor insulation is disposed over each of the conductors. At least a portion of the conductor insulation is in fluid communication with the local environment external to the lead via the apertures. | 2014-02-27 |
20140058488 | ELECTRICAL STIMULATION LEAD WITH JUNCTION AND METHODS OF MAKING AND USING - A lead arrangement includes a plurality of proximal leads, a distal lead, and a junction electrically and mechanically coupling the plurality of proximal leads to the at least one distal lead. Each proximal lead has a proximal end and a distal end and includes conductive contacts disposed along the proximal end and conductive wires coupled to the conductive contacts and extending to the distal end of the proximal lead. Each distal lead has a proximal end and a distal end and includes electrodes disposed along the distal end and conductive wires coupled to the electrodes and extending to the proximal end of the distal lead. The junction includes conductive tabs and a non-conductive material encapsulating the conductive tabs. The conductive wires of the at least one distal lead and the conductive wires of the plurality of proximal leads are attached to the conductive tabs of the junction. | 2014-02-27 |
20140058489 | ELECTRICALLY CONDUCTIVE AND MECHANICALLY SUPPORTIVE POLYMER MATERIALS FOR BIOMEDICAL LEADS - An implantable medical lead connecting to a device header of a medical apparatus and having an electrode, a conductor, and a conductive polymer layer formed on at least a portion of the medical lead. An insulative sheath surrounds the conductive polymer layer for electrical insulation. The conductive polymer layer and insulative sheath maintain mechanical and electrical continuity of the lead in the event of fracture. The conductive polymer layer is composed of conductive polymers and may contain one or more dopants for improving electrical characteristics, mechanical characteristics, and processability. | 2014-02-27 |
20140058490 | BIPOLAR SPINAL CORD STIMULATION TO ACTIVATE THE EXPIRATORY MUSCLES TO RESTORE COUGH - Methods and devices are provided for electrical stimulation of the expiratory muscles in humans or other mammals to produce cough in patients with spinal cord injuries resulting in paralysis of the expiratory muscles. An electrode, or a group of two or more electrodes (i.e. wire lead electrodes, disc electrodes, etc.) are positioned along the spinal cord, usually along the dorsal epidural surface. The electrodes can be located at different spinal cord levels and can be located in a parallel arrangement. Electrical stimulation, such as bipolar electrical stimulation, is then applied to activate the expiratory muscles and produce cough. | 2014-02-27 |
20140058491 | MRI COMPATIBLE CO-RADIALLY WOUND LEAD ASSEMBLY - An MRI compatible lead assembly construct is provided. The construct includes at least two filter components constructed from an electrode wire. One filter component may be a resonant LC filter at or near an electrode/wire interface that resolves the issue of insufficient attenuation by effectively blocking the RF induced current on the wire from exiting the wire through the electrode. The second filter component may include one or more non-resonant filter(s) positioned along the length of the electrode wire that resolve(s) the issue of excessive heating of the resonant LC filter by significantly attenuating the current induced on the wire before it reaches the resonant LC filter. The non-resonant filter(s) may also attenuate the RF current reflected from the resonant LC filter thereby resolving the issue of the strong reflected power from the resonant filter and the associated dielectric heating. | 2014-02-27 |
20140058492 | MRI COMPATIBLE ELECTRODE CIRCUIT - An MRI compatible electrode circuit construct is provided. The construct includes at least two filter components constructed from an electrode wire. One filter component may be a resonant LC filter at or near an electrode/wire interface that resolves the issue of insufficient attenuation by effectively blocking the RF induced current on the wire from exiting the wire through the electrode. The second filter component may include one or more non-resonant filter(s) positioned along the length of the electrode wire that resolve(s) the issue of excessive heating of the resonant LC filter by significantly attenuating the current induced on the wire before it reaches the resonant LC filter. The non-resonant filter(s) may also attenuate the RF current reflected from the resonant LC filter thereby resolving the issue of the strong reflected power from the resonant filter and the associated dielectric heating. | 2014-02-27 |
20140058493 | MRI COMPATIBLE ELECTRODE CIRCUIT - An MRI compatible electrode circuit construct is provided. The construct includes at least two filter components constructed from an electrode wire. One filter component may be a resonant LC filter at or near an electrode/wire interface that resolves the issue of insufficient attenuation by effectively blocking the RF induced current on the wire from exiting the wire through the electrode. The second filter component may include one or more non-resonant filter(s) positioned along the length of the electrode wire that resolve(s) the issue of excessive heating of the resonant LC filter by significantly attenuating the current induced on the wire before it reaches the resonant LC filter. The non-resonant filter(s) may also attenuate the RF current reflected from the resonant LC filter thereby resolving the issue of the strong reflected power from the resonant filter and the associated dielectric heating. | 2014-02-27 |
20140058494 | X-Ray Identification for Active Implantable Medical Device - An active implantable medical device is disclosed herein having a radio-opaque marker. The radio-opaque marker can be formed within an exterior wall of the device or within recesses on the outside of the exterior wall. The implantable medical device can be a leadless pacemaker. The shape of the radio-opaque marker can be designed to facilitate visualization and identification of the location, orientation, and rotation of the implanted medical device by conventional fluoroscopy. Methods of use are also disclosed. | 2014-02-27 |
20140058495 | PORTABLE ASSEMBLIES, SYSTEMS, AND METHODS FOR PROVIDING FUNCTIONAL OR THERAPEUTIC NEUROSTIMULATION - Neurostimulation assemblies, systems, and methods make possible the providing of short-term therapy or diagnostic testing by providing electrical connections between muscles and/or nerves inside the body and stimulus generators and/or recording instruments mounted on the surface of the skin or carried outside the body. Neurostimulation assemblies, systems, and methods may include a carrier and an electronics pod, the electronics pod including stimulation generation circuitry and user interface components. A power source and/or flash memory may be incorporated in neurostimulation assembly and/or the return electrode. The assemblies, systems, and methods are adapted to provide coordinated neurostimulation to multiple regions of the body. | 2014-02-27 |
20140058496 | DECELLULARIZED BIOLOGICALLY-ENGINEERED TUBULAR GRAFTS - This disclosure describes decellularized, biologically-engineered tubular grafts and methods of making and using such decellularized, biologically-engineered tubular grafts. | 2014-02-27 |
20140058497 | Deployment of Stents within Bifurcated Vessels - Systems and methods for deploying stents within bifurcated vessels in a true pantaloons configuration (Kamat technique) are disclosed. A device including a balloon catheter and a stent surrounding the catheter is inserted into a bifurcated blood vessel. The catheter includes a first lumen configured to accept a first guide wire, which exits the device at a distal end. The device is advanced within a main branch using the first guide wire until it reaches the carina, thus causing the second guide wire to enter a second side branch. The second wire exits the device at a tapered edge of the catheter from under the stent. The stent may then be deployed within the main branch. The stent may then be splayed across the carina with kissing balloons and the procedure may be completed with the kissing balloon deployment of two stents accurately at the carina in each side branch. | 2014-02-27 |
20140058498 | IMPLANT COMPRISING A NON-WOVEN FABRIC - The invention relates to a membrane implant for the treatment of vascular malformations, said implant being implantable by endovascular methods into the vessel to be treated, wherein the membrane implant consists of an expandable stent ( | 2014-02-27 |
20140058499 | Crush Recoverable Polymer Scaffolds - A medical device includes a polymer scaffold crimped to a catheter having an expansion balloon. The scaffold, after being deployed by the balloon, provides a crush recovery of about 90% after the diameter of the scaffold has been pinched or crushed by 50%. The scaffold has a pattern including an asymmetric closed cell connecting links connecting the closed cells. | 2014-02-27 |
20140058500 | RADIOPAQUE SUPER-ELASTIC INTRAVASCULAR STENT - The intravascular stent is formed from a composite wire includes an inner core of radiopaque metal, a polymer layer coaxially disposed about the inner core, and an outer metal layer coaxially disposed about the polymer layer. The intermediary polymer layer acts as a barrier material between the inner core and the outer sheath, so that the inner core and outer sheath may be made of dissimilar metallic layers, and the intermediary polymer layer will prevent a galvanic reaction between the inner core and the peripheral metal layer. The intravascular stent has ends flared radially outwardly to prevent radially and longitudinally inward deformation of the ends of the stent when the stent is disposed in a desired location in a patient's vasculature. | 2014-02-27 |
20140058501 | APPARATUS FOR TREATMENT OF CARDIAC VALVES AND METHOD OF ITS MANUFACTURE - A prosthetic valve including a replacement valve having a tubular valve body wall, an expandable stent having a framework with first and second ends, and suturing holding the framework to the valve body at the first and second ends. The suturing at the first end is colored differently from the suturing at the second end. | 2014-02-27 |
20140058502 | INTEGRATED HEART VALVE DELIVERY SYSTEM - Embodiments of the present disclosure provide a delivery apparatus for delivering a prosthetic heart valve to a native valve site via the human vasculature without the need for a separate introducer sheath. The delivery apparatus is particularly well-suited for advancing a prosthetic valve through the aorta (i.e., in a retrograde approach) for replacing a stenotic aortic valve. | 2014-02-27 |
20140058503 | ARTIFICIAL VALVE LEAFLET - An artificial mitral valve has a ring, an anterior cusp-side region, a posterior cusp-side region and a valve leaflet connected along an outer edge of the ring. The valve leaflet includes an anterior cusp forming member connected to the anterior cusp-side region and a posterior cusp forming member connected to the posterior cusp-side region. The anterior cusp forming member is provided with has an upper edge joined to the ring and a lower edge that forms a bifurcated portion. The upper edge is made up of a pair of right and left edges that incline inward and upward from the right and left sides, and a curved edge interposed between the inclined edges that curves along the anterior cusp-side region. The posterior cusp forming member has an upper edge joined to the ring and a lower edge that forms a bifurcated portion. | 2014-02-27 |
20140058504 | INSTRUMENT OF PATTERNING CUSP FOR CARDIAC VALVE RECONSTRUCTION AND COMPONENT THEREOF - In a case of repairing an aortic valve by forming a valve cusp with a biomembrane, the shape and the size of a valve cusp can be determined easily. An instrument including a valve cusp sizer for measuring the size of the valve cusp and a template for scribing lines for the shape of a valve cusp conforming to the measured size of the valve cusp, in which the valve cusp sizer has a plurality of differently-sized sizer blocks attached to each of the top ends of grip members respectively and each sizer block has an arcuate surface formed by cutting each of differently-sized circular cylinders at an angle conforming to the central angle for the commissure portions and, the template is formed with a scribing portion including a substantially semi-circular valve cusp base forming portion. | 2014-02-27 |
20140058505 | ADJUSTABLE ANNULOPLASTY RING SIZING INDICATOR - An adjustment tool enables manipulation of a prosthetic anatomical device such as an annuloplasty ring. The tool includes a compression member which is operative for retarding rotation of the adjustment shaft to preclude inadvertent rotation thereof during use of the tool by the surgeon. A locking device is associated with the adjustment tool to enable the releasable attachment of the tool to the anatomical device during its adjustment by manipulation of the tool. The locking device is oriented into operative and inoperative positions by the engagement and disengagement of locking elements. A scale may be provided on the adjustment tool to assist a surgeon in determining the size or amount of adjustment to the size of the anatomical device during its adjustment. | 2014-02-27 |
20140058506 | 3-COIL WIRELESS POWER TRANSFER SYSTEM FOR EYE IMPLANTS - A three-coil electromagnetic induction power transfer system is disclosed for epiretinal prostheses and other implants. A third, buffer coil is disposed between an external transmitting coil and a receiver coil buried within the body to improve efficiency and robustness to misalignments. One or more of the coils can be manufactured using micromechanical machining techniques to lay out conductors in a ribbon of biocompatible insulator, folding lengths of the insulated conductor traces longitudinally over one another, and then spiraling them into a ring. The traces change axial position in the ring by shifting across fold lines. One or more U-shaped sections on the traces can be folded so that adjacent traces can project opposite one another, lengthening the resulting ribbon that can be wound into a coil. | 2014-02-27 |
20140058507 | Intraocular Accommodating Lens and Methods of Use - Described herein are intraocular lenses and methods of implantation. In one aspect, the lens includes a shape changing optical element; a force translation element having a first end region coupled to the optical element and a second end region extending towards a ciliary structure, and an attachment portion coupled to the second end region of the force translation element and configured to contact the ciliary structure. The force translation element is configured to functionally transmit movements of the ciliary structure into a force exerted upon the optical element to effect an accommodating and a disaccommodating change of the optical element. | 2014-02-27 |
20140058508 | SYNTHETIC SCAFFOLDS AND ORGAN AND TISSUE TRANSPLANTATION - Articles, compositions, and methods for growing tissues and organs using bioreactors, including rotating bioreactors, are provided. Synthetic scaffolds for growing artificial tissue and organ transplants are also provided. | 2014-02-27 |
20140058509 | Medical Devices, Systems, and Kits for the Medialization of a Vocal Cord - Medical devices, systems, methods, and kits for the medialization of a vocal cord are described. An embodiment of a medical device comprises a proximal portion, a distal portion, and an elongate body extending from the proximal portion to the distal portion. The elongate body defines a thread extending from the proximal portion and the distal portion. | 2014-02-27 |
20140058510 | BONE IMPLANT - A bone implant can be made from a wire that defines an aperture for receiving a bone fixation means. The wire can be selected to stably fix a bone across a fracture location. | 2014-02-27 |
20140058511 | DYNAMIC SURGICAL IMPLANT - A surgical implant device capable of conforming to a variety of surface topographies facilitates the growth and regeneration of site to which the device is applied. The device employs a plurality of elongate members supporting a column of discrete, rotatable elements in contact with each adjacent element. Anchor plates secure the respective ends of the elongate members, such anchor plates attachable to bone. The implant device provides and ordered array of individually rotatable elements to form a surface that permits bodily fluids to pass therethough. | 2014-02-27 |
20140058512 | Intevertebral Implant - An intervertebral spacer for therapeutic treatment of a patient includes at least one link sized and dimensioned to fit within an intervertebral space in the patient, and is configured to maintain a separation of two adjacent vertebrae for a period of time. A rigid guiding object, which may be a tool or a successive link, is insertable into the patient, to guide other links into the patient using an MIS approach. A pivot is connected between successive links, or between a guide tool and a link, configured to limit a relative range of angular orientation between the link and the guiding tool, or successive links. Multiple links are so joined to form a chain pushable by the last link, and pullable by the first link, to form a chain which may be formed into a curved configuration corresponding to the patient's intervertebral space. | 2014-02-27 |
20140058513 | Intervertebral Implant - An intervertebral spacer for therapeutic treatment of a patient includes at least one link sized and dimensioned to fit within an intervertebral space in the patient, and is configured to maintain a separation of two adjacent vertebrae for a period of time. A rigid guiding object, which may be a tool or a successive link, is insertable into the patient, to guide other links into the patient using an MIS approach. A pivot is connected between successive links, or between a guide tool and a link, configured to limit a relative range of angular orientation between the link and the guiding tool, or successive links. Multiple links are so joined to form a chain pushable by the last link, and pullable by the first link, to form a chain which may be formed into a curved configuration corresponding to the patient's intervertebral space. | 2014-02-27 |
20140058514 | Insertion tool for Inter-body Vertebral Prosthetic Device With Self-Deploying Screws - An apparatus for inserting an intervertebral prosthesis within a spine of a mammal includes: a handle including a drive nut operating to produce rotational torque in response to user-input about a central axis; a first drive shaft including a proximal end in communication with the drive nut, receiving rotational torque therefrom, and imparting rotational torque to the first drive shaft about a first axis, which is laterally offset from the central axis; and a distal end of the first drive shaft including a first drive head; and a chuck disposed at a distal end of the tool for engaging the intervertebral prosthesis during implantation, wherein the first drive shaft extends through the chuck and the first drive head engages a first gear of the intervertebral prosthesis, such that rotation of the first gear causes rotation and deployment of a first anchoring element of the intervertebral prosthesis. | 2014-02-27 |
20140058515 | SURFACE EXPANDING SPACER - An interbody spacer comprising a series of stacked walls connected by a common base, wherein the spacer collapses when pressed into an access delivery tube. During insertion, the walls can flex as a unit, like bending a deck of cards, to traverse bends in the access tube. Upon distally exiting the portal of the access delivery tube, the walls track apart (like spreading fingers) to create a wide base of support for the vertebral body endplate. A graft delivery device that uses a conveyor belt-type approach to deliver bone graft from the device to a location in a patient. In some embodiments, the conveyor-belt is manually actuated. | 2014-02-27 |