47th week of 2014 patent applcation highlights part 56 |
Patent application number | Title | Published |
20140343590 | Device, And A Method For Treatment Of Increased Blood Pressure - Methods and devices are presented which act by cutting the renal nerves slowly through. The minimally invasive implantable devices can be delivered through state of the art delivery catheters into the renal arteries as known from stenting, and do not require external generators, thereby being easily to introduce in normal equipped radiology catheter labs. | 2014-11-20 |
20140343591 | ROLLER DEVICE - The invention relates to a device for inserting pigment into the skin comprising a roller head unit comprising 2 or more distal arms; a rotatable structure comprising needles extending therefrom, attached to said roller head unit between said distal arms; a tubular member attached to the proximal end of said roller head unit; an elastic element placed within the distal portion of the inner lumen of said tubular member; a pin placed within said tubular member proximal to said elastic element. | 2014-11-20 |
20140343592 | EMBOLISM FILTER WITH SELF-DEPLOYABLE GUIDEWIRE STOP - An embolism filter adapted to selectively stop an embolism filter along a length of guidewire, including a filter adapted to encircle a guidewire and at least one self-deploying stop attached to the filter and which selectively stops movement of said filter. | 2014-11-20 |
20140343593 | Catheter with Vessel Lining and Methods for Using Same - Systems for providing access across a site of obstruction and methods for manufacturing and using such systems. Such systems may include a sleeve having an inflation lumen; a bushing disposed in a distal section of the sleeve; and an everting member coupled to the sleeve with the bushing, the everting member being movable from an inverted position inside the sleeve to an everted position outside the sleeve in response to an increase in pressure in the inflation lumen. | 2014-11-20 |
20140343594 | MEDICAL DEVICE FOR MODIFICATION OF LEFT ATRIAL APPENDAGE AND RELATED SYSTEMS AND METHODS - A medical device and system for modifying a left atrial appendage (“LAA”), as well as related methods, are provided. In accordance with one embodiment, a medical device includes a plurality of frame segments coupled with at least one ring member, the at least one ring member having an inner surface defining notches radially spaced therein, each of the frame segments configured to be positioned within one of the notches of the at least one ring member to collectively form a frame structure. Each frame segment includes a hub portion and at least one leg portion, the hub portion having an upper surface configured to be captured in one of the notches defined in the at least one ring member, and the at least one leg portion extending from the hub portion. With this arrangement, a tissue growth member is coupled to the frame segments. | 2014-11-20 |
20140343595 | THROMBECTOMY DEVICE - The invention relates to a thrombectomy device with a substantially cylindrical stent structure ( | 2014-11-20 |
20140343596 | METHODS AND APPARATUS FOR FLOW RESTORATION - Methods for restoring blood flow in occluded blood vessels using an apparatus having a self-expandable distal segment that is pre-formed to assume a superimposed structure in an unconstrained condition but can be made to take on a volume-reduced form making it possible to introduce it with a microcatheter and a push wire arranged at the proximal end, with the distal segment in its superimposed structure assuming the form of a longitudinally open tube and having a mesh structure of interconnected strings or filaments or struts. In a preferred embodiment, the distal segment has a tapering structure at its proximal end where the strings or filaments or struts converge at a connection point. | 2014-11-20 |
20140343597 | MIGRATION RESISTANT EMBOLIC FILTER - An embolic filter is disclosed and can include a head. A plurality of bent legs can extend from the head. Each bent leg can be configured to engage an inner wall of a vein and prevent the embolic filter from migrating in a cranial direction. A plurality of straight legs can also extend from the head. Each straight leg can be configured to prevent the embolic filter from migrating in a caudal direction. | 2014-11-20 |
20140343598 | ENDOLUMINAL FILTER WITH FIXATION - An endoluminal filter including a first support member ( | 2014-11-20 |
20140343599 | Devices and Systems to Mitigate Traumatic Brain and Other Injuries Caused by Concussive or Blast Forces - A system for reducing the damaging effects of radiant energy, blast, or concussive events includes applying pressure to at least one jugular vein to reduce the egress of blood from the cranial cavity during or before the incidence of the imparting event. Reducing blood outflow from the cranial cavity increases intracranial volume and/or pressure of the cerebrospinal fluid to reduce the risk of traumatic brain injury and injuries to the spinal column. Reducing blood outflow further increases the intracranial pressure and volume, and thereby increases the pressure and volume of the cochlear fluid, the vitreous humor and the cerebrospinal fluid to thereby reduce the risk of injury to the inner ear, internal structure of the eye and of the spinal column. In addition, increasing intracranial pressure and volume reduces the likelihood of brain injury and any associated loss of olfactory function | 2014-11-20 |
20140343600 | MULTI-MODE INFLATABLE LIMB OCCLUSION DEVICE - Methods for adaptive cuff inflation for the purposes of occluding a limb of a subject include inflating a cuff to a pressure at or above limb occlusion pressure and periodically deflating the cuff to detect amplitude of oscillometric oscillations reaching or exceeding a predetermined threshold, whereby indicating that the cuff pressure has reached an updated systolic blood pressure. Selecting the cuff to be wide enough to define limb occlusion pressure at or below the systolic blood pressure assures that this maneuver does not compromise cessation of blood flow to the limb. Devices are disclosed configured to operate in at least two of the following three operating modes: a tourniquet mode, a remote conditioning mode and a blood pressure monitoring mode. | 2014-11-20 |
20140343601 | CLIP-BASED SYSTEMS AND METHODS FOR TREATING SEPTAL DEFECTS - Systems and methods for treating internal tissue defects, such as septal defects, with clip-based devices are provided. An exemplary clip-based device includes a tubular body having at least a first and a second deflectable member coupled thereto. The first and second members are coupled on opposite ends of the tubular body and configured to deflect between an undeployed configuration and a deployed configuration. In the deployed configuration, each member extends outwardly away from the tubular body in a position configured to abut a tissue surface. The first and second members are preferably configured to maintain a tissue wall therebetween and at least partially close any opening in the tissue wall. | 2014-11-20 |
20140343602 | EXPANDABLE OCCLUSION DEVICE AND METHODS - An occlusion device and method for occluding an undesirable passage through tissue, such as a septal defect, that provides an expandable cylinder or other structure that occludes the passage internally or by covering one or more openings to the passage. The occlusion device includes a wire lattice or mesh that expands from a contracted catheter-deliverable state to an expanded state that occludes the passage. The lattice or mesh has one or more layers, with layers that provide structural support to the device, and layers that provide a lattice braiding or pore sizes that promote further occlusion by a biological process, such as tissue ingrowth that further occludes the affected passage. | 2014-11-20 |
20140343603 | TROCAR SITE CLOSURE ASSEMBLY - Disclosed herein are trocar site closures, comprising a head with a plurality of arm receiving passages therethrough, an arm received by each of the passages, each passage having a discontinuity which allows each arm to be pulled inward but deters outward movement, and each arm having a grappling portion. The head and arms are inserted into a patient wound, such as a trocar site. The arms engage with tissue surrounding the wound. A pulling force is exerted on the arm proximal ends, drawing the distal ends of the arms toward the head and at least partially closing the wound. The head and at least a portion of the arms remain in the patient, and are preferably made of a biocompatible material. Also disclosed herein is an insertion device used to insert the closure into the wound and at least partially close the wound. | 2014-11-20 |
20140343604 | Soft Tissue Fixation Using A Looped Suture Construct - A looped suture construct is formed by looping a suture on itself and slidably connecting the suture through an anchoring structure such that a looped end and a free end of the suture are on opposite sides of the slidable connection. The anchoring structure may be bone, a suture anchor, or another structure securely attached to bone. The looped end and the free end are passed through the soft tissue to be repaired. The free end is then passed through the looped end. Tension is applied to the free end to draw the soft tissue into contact with the desired bone, whereupon the free end is secured to maintain the tension. The looped suture end remains open and positioned on one side or surface of the soft tissue. Suture anchors of the invention are pre-loaded with at least one suture having a looped end and at least one free end. | 2014-11-20 |
20140343605 | COMPOSITE ANCHOR - The present disclosure relates to a composite anchor. The anchor includes a cannulated proximal portion having a threaded outer surface and a distal portion coupled to the proximal portion, the distal portion including a top portion, a bottom portion, and a through hole, wherein the top portion is configured to be disposed within the cannulation of the proximal portion. | 2014-11-20 |
20140343606 | Adjustable Anchor Systems and Methods - An adjustable anchor system for securing tissue to bone, including an anchor having at least one passage extending from a proximal end toward a distal end. The passage defines a restriction such as a restricted opening. The anchor has at least one bone-engaging feature disposed between the proximal and distal ends. The system further includes a first material formed as a closed loop and capable of being placed through a portion of the tissue, and a second filament having a terminal end, a post limb and a sliding knot tied between the terminal end and the post limb to establish an elongated, adjustable-length loop which extends beyond the proximal end of the anchor and captures the closed loop of the first material. The knot of the second filament is restrained by the restricted opening when tension is applied as desired to the post limb to shorten the elongated loop to draw the tissue toward the anchor. | 2014-11-20 |
20140343607 | Surgical Filament Snare Assemblies - A surgical filament snare assembly including an anchor capable of being fixated in bone and having a filament engagement feature. A first filament has a noose on a first portion of at least a first limb and has a second portion connected to the filament engagement feature of the anchor. Preferably, at least one free filament limb, which in some embodiments is a length of the first filament and in other embodiments is a second filament, is capable of being passed through tissue to be repaired and has at least one end passable through the noose to enable incremental tensioning of the tissue after the anchor is fixated in bone. The noose strangulates the free filament limb when tension is applied to at least one of the free filament limb and the noose. | 2014-11-20 |
20140343608 | EXPANSION INTERSPINOUS FIXATION DEVICE AND METHOD - A device and method for performing interspinous fixation or spinal fusion is provided. The device may generally include a first plate and a second plate, each having an adjustable length, and a mechanical actuator for increasing or reducing the length of the plates and, correspondingly, the device. Operation of the mechanical actuator causes first and second inner expansion portions of each plate to simultaneously slide on an outer fixed portion of the plate, to increase or decrease (depending on the direction of operation of the mechanical actuator) the separation between the first and second inner expansion portions, and thus, lengthen or shorten the plates and device. | 2014-11-20 |
20140343609 | Flexible Spine Stabilization System - A system for flexibly stabilizing a vertebral motion segment by connecting a first vertebra and a second vertebra is disclosed. The system includes an elongate connection element with end portions interconnected by a flexible coupling member. The system includes first and second attachment portions for connecting the connection element to the vertebrae. A first resilient member is positioned between the first end portion and the first attachment portion, and a second resilient member is positioned between the first attachment portion and the second attachment portion. The system is designed such that the second resilient member is compressed when the first and second attachment portions move towards each other, and the first resilient member is compressed when the first and second attachment portions extend away from each other. | 2014-11-20 |
20140343610 | DYNAMIC SPINAL STABILIZATION ASSEMBLY WITH ELASTIC BUMPERS AND LOCKING LIMITED TRAVEL CLOSURE MECHANISMS - A dynamic stabilization assembly includes a core, typically in the form of a tensioned cord, at least one pair of bone anchors, a spacer surrounding the core located between the bone anchors, at least one elastic bumper and at least one fixing or blocking member. The core is slidable with respect to at least one of the bone anchors, the spacer and the bumper. The bumper is compressed. Bone screws of the assembly include closure structures that lock against the bone screw independent of any fixing or sliding of the core with respect to the bone screw. | 2014-11-20 |
20140343611 | NON-INVASIVE ADJUSTABLE DISTRACTION SYSTEM - A spinal distraction system includes a distraction rod having a first end and a second end, the first end being configured for affixation to a subject's spine at a first location, the distraction rod having a second end containing a recess having a threaded portion disposed therein. The system further includes an adjustable portion configured for affixation relative to the subject's spine at a second location remote from the first location, the adjustable portion comprising a housing containing a magnetic assembly, the magnetic assembly affixed at one end thereof to a lead screw, the lead screw operatively coupled to the threaded portion. A locking pin may secure the lead screw to the magnetic assembly. An o-ring gland disposed on the end of the housing may form a dynamic seal with the distraction rod. | 2014-11-20 |
20140343612 | SPINAL CORRECTION SYSTEM - A spinal construct comprises a longitudinal member extending between a first end and a second end and including an intermediate portion. A construct member includes a first surface and a second surface movable relative to the first surface in a configuration for connection with a first portion of vertebral tissue. The construct member defines an implant cavity configured for disposal of the first end. Systems and methods are disclosed. | 2014-11-20 |
20140343613 | BONE ANCHORING MEMBER WITH CLAMP MECHANISM - A multi-piece disc replacement implant for replacing a disc removed by a discectomy including an upper plate member, a lower plate member, and an intermediate resilient member providing movement between te two plate members replicating the natural movement of the spine. The plate members are rigid and have orthogonal sidewalls forming an enclosure. The resilient member is an elastic solid or a multi-chamber balloon structure of fluid-filled sacks that collectively define a non-uniform shape such as an oblate spheroid, or a helically coiled string of beads. Such an implant is capable of supporting the compressive and cyclic loads required of a natural disc. The upper and lower plate members are cooperatively formed to selectively limit the allowable range of motion in any given direction and a provided with protrusions to be received in one or more channels cooperatively formed in the vertebrae and secured in place by a bone screw. | 2014-11-20 |
20140343614 | DENTAL OCCLUSION AND TENSION BAND TIES, SYSTEMS AND METHODS - Embodiments relate to devices, systems, kits and methods for achieving maxillo-mandibular fixation (MMF). In an embodiment, a system comprises a plurality of dental occlusion ties and/or tension band ties (referred to herein as “DO ties” and “TB ties,” respectively). In another embodiment, a system or kit can comprise a plurality of one or both of DO ties and/or TB ties as well as a trimming tool, comfort caps or material, a lip/cheek retractor, and/or an instruction sheet. DO ties and TB ties can simplify the management of mandible fractures and maxilla fractures by helping re-establish precise dental occlusion for MMF. | 2014-11-20 |
20140343615 | METHOD AND SYSTEM FOR STORING AND INSERTING AN IMPLANT - An implant storage and insertion system for a shape memory orthopedic implant allows the implant to be constrained in a deformed state, protected, insulated, held for insertion, and properly positioned in bone. The implant storage and insertion system includes a restraining block having an impact surface. The restraining block engages an implant at a first end, and further a medical instrument engages the restraining block and positions the restraining block at a bone such that the impact surface may be impacted to insert a second end of the implant into the bone. | 2014-11-20 |
20140343616 | ARTHRODESIS COMPRESSION DEVICE - A device for compression in arthrodesis is provided. The device is generally comprised of two screws, a proximal screw and a distal screw, the distal screw being configured to connect to the proximal screw. The proximal screw may have two portions, one portion with external bone threads, and one cylindrical portion. The two portions of the proximal screw may be formed such that they form an angle desirable for arthrodesis, or permanent fixation, of the joint. The distal screw may be inserted into the proximal screw, and may be further provided with additional external bone threads to provide compression at the joint site. | 2014-11-20 |
20140343617 | UNIPLANAR SCREW ASSEMBLY AND METHODS OF USE - The screw assembly includes a screw, an insert, and a body member. The screw includes a longitudinal axis and a proximal end with a head portion and a distal end with a threaded portion. The insert operably couples with the head portion and is configured to rotate relative to the head portion about the longitudinal axis. The body member operably couples with the insert and is configured to pivot relative to the insert in a single plane parallel to the longtudinal axis. In other features, the body member operably couples with the insert and is configured to pivot relative to the insert about a transverse axis normal to a plane parallel to the longtudinal axis. | 2014-11-20 |
20140343618 | SAMPLING INTRINSIC AV CONDUCTION TIME - Methods and/or devices for sampling a patient's intrinsic AV conduction time during cardiac therapy that may, e.g., change the AV delays to values based on the AV delays themselves, previously-sampled intrinsic AV conduction times, and/or one or more other parameters directly related to AV delays to provide a time period during which to measure the patient's intrinsic AV conduction time. | 2014-11-20 |
20140343619 | IMPLANTABLE CARDIAC RESYNCHRONIZER WITH BIVENTRICULAR PACING AND DETECTION OF LOSS OF CAPTURE AND ANODAL STIMULATION - An medical device for stimulating the heart using biventricular stimulation. The device includes a sensor for detecting an endocardial acceleration parameter and a processing circuit configured to receive the endocardial acceleration parameter. The device further includes stimulation electronics coupled to the processing circuit. The processing circuit is configured to use the EA parameter to evaluate the biventricular stimulation. The evaluation includes comparing the value of the EA parameter in biventricular mode to the value of the EA parameter in left only mode or right only mode, and using the comparison and an assessment of the variability of the EA parameter as a function of the AVD in the left or right mode to distinguish between cases comprising: (a) normal operation, (b) a loss of RV or LV capture, (c) possible anodal stimulation. The processing circuit is further configured to conduct at least one update to operational parameters of the device based on the determined case. | 2014-11-20 |
20140343620 | LEADLESS CARDIAC STIMULATION DEVICE EMPLOYING DISTRIBUTED LOGIC - Systems and methods involve an intrathoracic cardiac stimulation device operable to provide autonomous cardiac sensing and energy delivery. The cardiac stimulation device includes a housing configured for intrathoracic placement relative to a patient's heart. A fixation arrangement of the housing is configured to affix the housing at an implant location within cardiac tissue or cardiac vasculature. An electrode arrangement supported by the housing is configured to sense cardiac activity and deliver stimulation energy to the cardiac tissue or cardiac vasculature. Energy delivery circuitry in the housing is coupled to the electrode arrangement. Detection circuitry is provided in the housing and coupled to the electrode arrangement. Communications circuitry may optionally be supported by the housing. A controller in the housing coordinates delivery of energy to the cardiac tissue or cardiac vasculature in accordance with an energy delivery protocol appropriate for the implant location. | 2014-11-20 |
20140343621 | PROBE SYSTEM FOR BRAIN APPLICATIONS - The present invention relates to a probe system for brain applications, especially for neurostimulation and/or neurorecording, comprising at least one lead for brain applications with a first number of stimulation and/or recording electrodes, the lead being connectable to a low-count connector element or having a low-count connector element, whereby the low-count connector element has a second number of connector contacts, whereby the second number of connector contacts is lower than the first number of the electrodes, whereby the low-count connector element is configured such that the low-count connector element can be directly and/or indirectly connected to at least one pulse generator, whereby the probe system further comprises a power-management unit, a controller unit, a communication unit, and a switching unit. Furthermore, the present invention relates to a deep brain stimulation system, a low-count connector element, and to a method of manufacturing a probe system for a deep brain stimulation system. | 2014-11-20 |
20140343622 | SELECTIVE HIGH FREQUENCY SPINAL CORD MODULATION FOR INHIBITING PAIN WITH REDUCED SIDE EFFECTS, AND ASSOCIATED SYSTEMS AND METHODS - Selective high-frequency spinal cord modulation for inhibiting pain with reduced side effects and associated systems and methods are disclosed. In particular embodiments, high-frequency modulation in the range of from about 1.5 KHz to about 50 KHz may be applied to the patient's spinal cord region to address low back pain without creating unwanted sensory and/or motor side effects. In other embodiments, modulation in accordance with similar parameters can be applied to other spinal or peripheral locations to address other indications. | 2014-11-20 |
20140343623 | METHODS AND SYSTEMS FOR AUTOMATICALLY TURNING ON AND OFF DRG STIMULATION AND ADJUSTING DRG STIMULATION PARAMETERS - Methods and systems described herein can be used to automatically turn on and off stimulation of a target dorsal root ganglion (DRG) and/or adjust stimulation parameters. At least one of an input signal (indicative of an electrical field resulting from an electrical signal propagated by adjacent distal sensory nerve fibers toward the target DRG), an output signal (indicative of an electrical field resulting from an electrical signal propagated by adjacent proximal sensory nerve fibers away from the target DRG) or a DRG signal (indicative of an electrical field produced by cell bodies of primary sensory neurons within the target DRG and resulting from an electrical signal propagated by sensory nerve fibers within the target DRG) is/are obtained and analyzed. Delivery of electrical stimulation is turned on and off and/or at least one of pulse amplitude, pulse width and/or pulse repetition rate is/are adjusted based on results of the analysis. | 2014-11-20 |
20140343624 | NEUROMODULATION OF SUBCELLULAR STRUCTURES WITHIN THE DORSAL ROOT GANGLION - Devices, systems and methods are provided for the targeted treatment of abnormal sensory conditions. In such conditions, physical stimuli is transduced into neuronal impulses that are subsequently transmitted to the central nervous system for processing. Such transduction is achieved by primary sensory neurons in the dorsal root ganglions. Subcellular structures on primary sensory neurons can significantly modulate the function of these neurons, thereby affecting the transduction and reducing the abnormal sensory experiences. Thus, devices, systems and methods are provided for neuromodulating subcellular structures on primary sensory neurons of the dorsal root ganglions. | 2014-11-20 |
20140343625 | MUSCLE STIMULATION DEVICE - A surface NMES stimulation device the device has a control processor, a voltage regulator connected to a high voltage supply, a bridge of control switches, and electrodes or electrode terminals connected in the bridge to receive drive signals via the control switches. The processor directs a drive scheme for the bridge control switches in which charge build-up on a user's skin is allowed to dissipate to ground in an inter-pulse interval. An isolation capacitor isolates the high voltage supply from the electrodes, and charging of the capacitor only occurs if a switch allows it. Sensors senses supply voltage and bridge current and the processor monitors there to determine further stimulation and faults. | 2014-11-20 |
20140343626 | RETENTION OF A MAGNET IN A COCHLEAR IMPLANT - A system for retaining a magnet in a cochlear implant, comprising a retainer embedded within an encapsulant of the cochlear implant, and a magnet case engaged with the retainer. A retainer for retaining a magnet within a cochlear implant comprising a number of first fasteners that couple with a number of corresponding second fasteners of a magnet case hermetically sealing the magnet, and a number of supports embedded within an encapsulant of the cochlear implant. | 2014-11-20 |
20140343627 | METHOD AND SYSTEM FOR MODULATING EATING BEHAVIOR BY MEANS OF NEURO-ELECTRICAL CODED SIGNALS - Method and systems modulating eating behavior comprising (i) generating at least one confounding neuro-electrical signal that is adapted to modulate the sense of taste in the body, (ii) generating at least one confounding neuro-electrical signal that is adapted to modulate the sense of smell in the body, and (ii) transmitting at least one of the confounding neuro-electrical signals to a subject to modulate the subject's sense of taste or smell. In a preferred embodiment, both confounding neuro-electrical signals are transmitted to the subject to modulate the subject's sense of taste and smell. | 2014-11-20 |
20140343628 | AUTOMATIC CURRENT BALANCING WITH LOCK CONTROL FOR A CLINICIAN PROGRAMMER - A method of programming electrodes includes automatic current balancing and lock control. A virtual representation of a lead is displayed. The lead includes a plurality of electrodes. A subset of the electrodes is selected for programming. Each of the electrodes in the subset has one of two polarities. The two polarities are anode and cathode. A first percentage of a total stimulation current is assigned to a first one of the electrodes in the subset. In response to a user input, the first percentage is fixed to the first electrode. A plurality of second electrodes in the subset that have the same polarity as the first electrode is identified. Thereafter, a respective second percentage of the total stimulation current is automatically assigned to each of the second electrodes. A sum of the first percentage and the respective second percentages is equal to 100%. | 2014-11-20 |
20140343629 | METHOD AND APPARATUS FOR DISPLAYING A GRAPHICAL IMPEDANCE HISTORY FOR OUTPUT CHANNELS OF A LEAD - A method of displaying impedance information of an implantable medical device is provided. One or more impedance values are received over a period of time for a plurality of channels. The channels may each include an electrode contact on an implantable lead. A graph is displayed that illustrates a variation of the impedance values over at least a portion of the period of time for one or more of the channels. A visual landscape that is representative of the impedance values for the plurality of channels is also displayed. | 2014-11-20 |
20140343630 | ARBITRARY WAVEFORM GENERATOR & NEURAL STIMULATION APPLICATION - A method, device and/or system for generating arbitrary waveforms of a desired shape that can be used for generating a stimulation pulse for medical purposes such as for spinal cord stimulation therapy. | 2014-11-20 |
20140343631 | CONNECTOR ASSEMBLIES FOR IMPLANTABLE STIMULATORS - Exemplary systems include a stimulator configured to be implanted within a patient, the stimulator having a body defined by at least one side surface disposed in between distal and proximal end surfaces, and a connector assembly configured to be coupled to the stimulator and extend parallel to the at least one side surface of the stimulator. The connector assembly is further configured to facilitate removable coupling of a lead having one or more electrodes disposed thereon to the stimulator. | 2014-11-20 |
20140343632 | TRANSVASCULAR NERVE STIMULATION APPARATUS AND METHODS - Electrode structures for transvascular nerve stimulation combine electrodes with an electrically-insulating backing layer. The backing layer increases the electrical impedance of electrical paths through blood in a lumen of a blood vessel and consequently increases the flow of electrical current through surrounding tissues. The electrode structures may be applied to stimulate nerves such as the phrenic, vagus, trigeminal, obturator or other nerves. | 2014-11-20 |
20140343633 | ELECTRICALLY IDENTIFIABLE ELECTRODE LEAD AND METHOD OF ELECTRICALLY IDENTIFYING AN ELECTRODE LEAD - An electrically identifiable medical electrode lead. The lead includes a flexible lead body having a distal end and a connector end. The lead also includes a plurality of electrodes disposed near the distal end of the flexible lead body. The lead further includes a connector disposed at the connector end of the flexible lead body, the connector including a plurality of contacts. The lead additionally includes a plurality of conductors supported by and passing through the flexible lead body, the plurality of conductors including electrical conductors that provide paths for electrical current from the connector to the plurality of electrodes. Finally, the lead includes a memory circuit supported by the flexible lead body and being in electrical communication with a contact of the plurality of contacts in the connector. | 2014-11-20 |
20140343634 | Self Resonant Transmitting Device - A device for powering an implant within a body of a subject from a location external to the subject, wherein the implant requires a threshold rate of power increase in order to operate in at least one mode, may include an antenna configured to wirelessly transmit energy to the implant. The device may also include a power storage unit configured to store energy from a power source incapable of delivering the threshold rate of power increase to enable the implant unit to operate in the at least one mode and a power release unit configured to release a pulse of energy from the power storage unit to the antenna after the power storage unit collects an amount of energy sufficient to enable the implant unit to operate in the at least one mode. | 2014-11-20 |
20140343635 | TRANSVASCULAR NERVE STIMULATION APPARATUS AND METHODS - Electrode structures for transvascular nerve stimulation combine electrodes with an electrically-insulating backing layer. The backing layer increases the electrical impedance of electrical paths through blood in a lumen of a blood vessel and consequently increases the flow of electrical current through surrounding tissues. The electrode structures may be applied to stimulate nerves such as the phrenic, vagus, trigeminal, obturator or other nerves. | 2014-11-20 |
20140343636 | TRANSVASCULAR NERVE STIMULATION APPARATUS AND METHODS - Electrode structures for transvascular nerve stimulation combine electrodes with an electrically-insulating backing layer. The backing layer increases the electrical impedance of electrical paths through blood in a lumen of a blood vessel and consequently increases the flow of electrical current through surrounding tissues. The electrode structures may be applied to stimulate nerves such as the phrenic, vagus, trigeminal, obturator or other nerves. | 2014-11-20 |
20140343637 | CONTROL OF NEURAL MODULATION THERAPY USING CERVICAL IMPEDANCE - An implantable apparatus can comprise an electrical test energy delivery circuit configured to provide an electrical test signal to a cervical location in a patient body. A detector circuit can use the electrical test signal to detect cervical impedance and generate a cervical impedance signal representing fluctuations in the detected cervical impedance. The implantable apparatus can comprise a therapy delivery circuit, such as configured to provide electrical neural modulation therapy using a neural modulation timing parameter, and a processor circuit that can be coupled to the electrical test energy delivery circuit, the detector circuit, and the therapy delivery circuit. The processor circuit can be configured to determine a pulsatile signal or pulse pressure signal, such as using the cervical impedance signal, identify a characteristic of the pulsatile signal or pulse pressure signal, and control a neural modulation therapy using the timing parameter and the identified pulse pressure signal characteristic. | 2014-11-20 |
20140343638 | NON-INVASIVE METHOD FOR SLIMMING A HUMAN BODY USING LASER ENERGY OF WAVELENGTHS SHORTER THAN 632 NM - A noninvasive method of slimming a patient's body by applying laser energy having a wavelength shorter than 632 nm externally through the skin of the patient. One or more areas of a patient's body, preferably the more fatty regions, such as the abdominal, buttock, lower back, thigh, bust or arm regions, is measured. Objective measurements are made of body criteria, including external dimension, percentage body fat, fat mass, or body mass. Sufficient laser energy, preferably in a range of 0.03-0.1 J/cm | 2014-11-20 |
20140343639 | Thermal Control System - A thermal control unit for delivering temperature-controlled fluid to one or more patient therapy devices (e.g. pads, blankets, etc.) that are in contact with a patient is disclosed. The thermal control unit allows multiple patient therapy devices to be fluidly coupled thereto and to individually monitor the temperatures, flow rates, and/or connections/disconnections of the patient therapy devices. A user interface enables a user to designate outlet ports to the therapy devices as active or inactive, and the control unit provides notifications to the user if any of the active ports experience an undesired condition, or if a patient therapy device is connected to an inactive port. The user interface further allows the user to designate one of multiple patient temperature probes as a primary probe. The primary probe is used to control the temperature of the fluid circulating through the control unit. | 2014-11-20 |
20140343640 | SYSTEMS AND METHODS FOR REDUCING BODY TEMPERATURE - Systems and methods for lowering the body temperature of a patient or inducing hypothermia are generally described. In certain embodiments, the core body temperature of a patient can be lowered by using a heat exchanger. In certain embodiments, the heat exchanger of configured to facilitate transfer of heat from an intubation gas to a cooling fluid prior to delivering the intubation gas to the patient (e.g., to the patient's lungs). | 2014-11-20 |
20140343641 | METHODS AND DEVICES FOR NON-INVASIVE CEREBRAL AND SYSTEMIC COOLING - Methods for cerebral cooling are described. Cooling assemblies include elongate tubular members, a reservoir containing a pressurized fluid, and a manifold connecting the reservoir and elongate tubular members. After insertion of the elongate tubular members into the patient's nostrils, a pressurized fluid is delivered onto a surface of the patient's nasal cavity through a plurality of ports in the elongate tubular members. The delivery of the fluid causes cooling by direct heat transfer through the nasopharynx and hematogenous cooling through the carotids and the Circle of Willis. | 2014-11-20 |
20140343642 | Device for treating diseases - A method for treating a disease such as an infectious disease, a cancer or asthma, comprising administering to a patient a stay in a Faraday cage. | 2014-11-20 |
20140343643 | IMPLANTABLE ELECTRODE ARRAY ASSEMBLY INCLUDING A CARRIER WITH EMBEDDED CONTROL MODULES CONTAINED IN PACKAGES, THE PACKAGES EXTENDING OUTWARDLY SO AS TO EXTEND OVER THE CARRIER - An implantable electrode array that includes a carrier on which multiple spaced apart electrodes are disposed. Embedded in the module are control modules. The control modules are contained in packages. Portions of the packages extend outwardly from the carrier so as to be disposed against adjacent surfaces of the carrier. The packages contain conductive tracts that provide conductive links from the conductors internal to the carrier to the packaged control modules. | 2014-11-20 |
20140343644 | MEDICAL LEADS AND TECHNIQUES FOR MANUFACTURING THE SAME - In some examples, the disclosure relates to a medical device comprising a lead including an electrically conductive lead wire; and an electrode electrically coupled to the lead wire, the electrode including a substrate and a coating on an outer surface of the substrate, wherein the lead wire is formed of a composition comprising titanium or titanium alloys, wherein the substrate is formed of a composition comprising one or more of titanium, tantalum, niobium, and alloys thereof, wherein the coating comprises at least one of Pt, TiN, IrOx, and poly(dioctyl-bithiophene) (PDOT). In some examples, the lead wire may be coupled to the lead wire via a weld, such as, e.g., a laser weld. | 2014-11-20 |
20140343645 | ELECTRICAL STIMULATION LEADS AND SYSTEMS WITH ANCHORING UNITS AND METHODS OF MAKING AND USING - An electrical stimulation lead includes a lead body having a distal end portion, a proximal end portion, and a longitudinal length; electrodes disposed along the distal end portion of the lead body; terminals disposed along the proximal end portion of the lead body; conductors electrically coupling the terminals to the electrodes; and at least one anchoring unit disposed along the distal end portion of the lead body. Each anchoring unit includes a cylindrical lead attachment element defining a central lumen within which a portion of the lead is received, and at least one anchoring element this is disposed over the lead attachment element and extends away from the lead attachment element and is configured and arranged for contact with patient tissue to anchor the lead within the patient tissue. | 2014-11-20 |
20140343646 | DUAL SIDE LOAD ANCHOR FOR ELECTRODE LEAD, SYSTEMS CONTAINING THE ANCHOR, AND METHODS OF MAKING AND USING - An implantable lead anchor includes a first anchor shell and a second anchor shell. The first and second anchor shells define two parallel lead channels. The lead anchor also includes an actuating mechanism to operably adjust the first and second anchor shells between a load position and a lock position. In the lock position, the first and second anchor shells are closer together than in the load position and any lead disposed within one of She two parallel lead channels is locked in place. In the load position, the first and second anchor shells are sufficiently spaced apart so that a portion of a lead can be side-loaded between the first and second anchor shells. The lead anchor also includes at least one guide element that extends between the first and second anchor shells to maintain an orientation of the first and second anchor shells relative to each other. | 2014-11-20 |
20140343647 | SYSTEMS AND METHODS FOR MAKING AND USING TIP ELECTRODES FOR LEADS OF ELECTRICAL STIMULATION SYSTEMS - An implantable electrical stimulation lead includes a lead body, electrodes disposed along a distal end of the lead body, terminals disposed along the proximal end of the lead body, and conductors coupling the terminals to the electrodes. The electrodes include a tip electrode having an electrode body with an outer stimulating surface. An internal lumen is defined in the electrode body and extends inwardly from an opening in a proximal end of the electrode body. Side apertures are formed between the outer stimulating surface and the internal lumen. A portion of the lead body is disposed within the internal lumen and side apertures through the opening in the proximal end of the electrode body. That portion of the lead body facilitates retention of the tip electrode on a distal tip of the lead body. | 2014-11-20 |
20140343648 | CONTACTING ARRANGEMENT COMPRISING A FEEDTHROUGH AND A FILTER STRUCTURE AND METHOD OF MAKING - One aspect relates to a contacting arrangement for use in a housing of a medically implantable apparatus. Said contacting arrangement includes an electrical feedthrough device that includes at least one electrically insulating main feedthrough member and at least one electrical conducting element. The conducting element is designed to establish at least one electrically conducting connection between an interior of the housing and an exterior through the main feedthrough member. The conducting element is hermetically sealed with respect to the main feedthrough member. The at least one conducting element comprises at least one cermet. The contacting arrangement further includes an electrical filter structure which is arranged on a face of the feedthrough device. Furthermore, said filter structure is connected to the conducting element by means of at least one electrical surface connection. | 2014-11-20 |
20140343649 | METHOD TO ENHANCE ELECTRODE LOCALIZATION OF A LEAD - An exemplary method includes positioning a lead in a patient where the lead has a longitudinal axis that extends from a proximal end to a distal end and where the lead includes an electrode with an electrical center offset from the longitudinal axis of the lead body; measuring electrical potential in a three-dimensional potential field using the electrode; and based on the measuring and the offset of the electrical center, determining lead roll about the longitudinal axis of the lead body where lead roll may be used for correction of field heterogeneity, placement or navigation of the lead or physiological monitoring (e.g., cardiac function, respiration, etc.). Various other methods, devices, systems, etc., are also disclosed. | 2014-11-20 |
20140343650 | METHOD TO ENHANCE ELECTRODE LOCALIZATION OF A LEAD - An exemplary method includes positioning a lead in a patient where the lead has a longitudinal axis that extends from a proximal end to a distal end and where the lead includes an electrode with an electrical center offset from the longitudinal axis of the lead body; measuring electrical potential in a three-dimensional potential field using the electrode; and based on the measuring and the offset of the electrical center, determining lead roll about the longitudinal axis of the lead body where lead roll may be used for correction of field heterogeneity, placement or navigation of the lead or physiological monitoring (e.g., cardiac function, respiration, etc.). Various other methods, devices, systems, etc., are also disclosed. | 2014-11-20 |
20140343651 | METHOD TO ENHANCE ELECTRODE LOCALIZATION OF A LEAD - An exemplary method includes positioning a lead in a patient where the lead has a longitudinal axis that extends from a proximal end to a distal end and where the lead includes an electrode with an electrical center offset from the longitudinal axis of the lead body; measuring electrical potential in a three-dimensional potential field using the electrode; and based on the measuring and the offset of the electrical center, determining lead roll about the longitudinal axis of the lead body where lead roll may be used for correction of field heterogeneity, placement or navigation of the lead or physiological monitoring (e.g., cardiac function, respiration, etc.). Various other methods, devices, systems, etc., are also disclosed. | 2014-11-20 |
20140343652 | METHOD TO ENHANCE ELECTRODE LOCALIZATION OF A LEAD - An exemplary method includes positioning a lead in a patient where the lead has a longitudinal axis that extends from a proximal end to a distal end and where the lead includes an electrode with an electrical center offset from the longitudinal axis of the lead body; measuring electrical potential in a three-dimensional potential field using the electrode; and based on the measuring and the offset of the electrical center, determining lead roll about the longitudinal axis of the lead body where lead roll may be used for correction of field heterogeneity, placement or navigation of the lead or physiological monitoring (e.g., cardiac function, respiration, etc.). Various other methods, devices, systems, etc., are also disclosed. | 2014-11-20 |
20140343653 | MEDICAL ELECTRICAL LEAD - An improved medical electrical lead is disclosed herein. The lead may include a longitudinally extending body having a distal end, a proximal end, a conductive element extending between the distal and proximal ends, and an electrode coupled to the conductive element utilizing a reflow process. The conductive element and electrode may comprise materials that are incompatible. | 2014-11-20 |
20140343654 | IMPLANTABLE MEDICAL ELECTRICAL LEAD CONDUCTORS AND CONSTRUCTION METHODS - A coiled continuous conductor wire of an implantable medical electrical lead includes a first, electrode length and a second, insulated length, wherein the insulated length of the wire has a radial cross-section defined by a round profile, while the electrode length of the wire has a radial cross-section defined by a flattened profile, a long axis edge of which defines an outer diameter surface of the electrode length. The radial cross-section profile, along the electrode length of wire, is preferably flattened after an entire length of the wire has been coiled. | 2014-11-20 |
20140343655 | SYSTEM AND METHOD FOR SPINAL CORD MODULATION TO TREAT MOTOT DISORDER WITHOUT PARESTHESIA - A method for of performing a medical procedure on a patient suffering from a movement disorder. The method comprises delivering electrical current having a defined pulse rate equal to or greater than 1500 Hz and/or a defined pulse duration equal to or less than 200 Hz to spinal cord tissue of the patient in a manner that modulates neuronal traffic in at least one dorsal column (DC) nerve fiber of the patient, thereby treating symptoms of the movement disorder without causing the patient to perceive paresthesia from the delivered electrical current. | 2014-11-20 |
20140343656 | ELECTRICAL STIMULATION LEADS WITH ANCHORING UNIT AND ELECTRODE ARRANGEMENT AND METHODS OF MAKING AND USING - An electrical stimulation lead includes a lead body having a distal end portion, a proximal end portion, and a longitudinal length; and electrodes disposed along the distal end portion of the lead body. The electrodes include a first set of electrodes and a second set of electrodes. The electrodes of the first set are spaced apart by a first distance and the electrodes of the second set are spaced apart by a second distance that is greater than the first distance and the first set is spaced apart from the second set by a third distance that is greater than or equal to the second distance. The lead also includes terminals disposed along the proximal end portion of the lead body; conductors electrically coupling the terminals to the electrodes; and anchoring units disposed along the distal end portion of the lead body and proximal to the first set of electrodes. | 2014-11-20 |
20140343657 | ATRAUMATIC ELECTRODE LEAD - A cochlear implant includes a processor, an array of electrodes disposed along a flexible body and a lead body connecting the processor to the array of electrodes. The lead body includes a first tube having a first outside diameter, a second tube having a second outside diameter smaller than the first diameter, a portion of the second tube being disposed within the first tube, and wires passing through the first tube and the second tube, the wires comprising a helically coiled portion. A method for forming a lead body is also provided. | 2014-11-20 |
20140343658 | STENT-GRAFT WITH PROXIMAL AND DISTAL ATTACHMENT, DELIVERY CATHETER AND METHODS OF MAKING SAME - A metallic or pseudometallic covered stent in which the stent component and the cover component are each fabricated of biocompatible metallic or pseudometallic materials, in which the cover and the stent are joined by at least one juncture at each of a proximal and distal end of the stent and the cover. A method of joining the stent and the cover is also disclosed. | 2014-11-20 |
20140343659 | DELIVERY AND RELEASE DEVICE FOR STENT-GRAFT - A delivery and release device for stent-graft includes a guiding head and a central tube connected thereto, an outer tube sleeving on the outside of the central tube, a positioning tube sheathed between the central tube and the outer tube, a front fixator, a back fixator and a positioner successively sheathed between the positioning tube and the outer tube. The stent-graft is placed between the back fixator and the positioner. A metal bar is connected to the guiding head along its axial direction with a ring suture being connected to the front fixator. The ring suture sleeves onto the metal bar after passing through the stent-graft. During the release process, the metal bar moves forward in the axial direction to detach from the ring suture, thereby the stent-graft is released. | 2014-11-20 |
20140343660 | STENT DELIVERY SYSTEM - An operating unit in a stent delivery system comprises a displacement body including a first body connected to an outer tube body and a second body which is connected to the first body and meshed with a rotary roller. A first connection surface of the first body is formed with a first convex portion and a first concave portion recessed relative to the first convex portion. The first convex portion engages a second concave portion of the second body and a second convex portion engages the first concave portion. When movement of the displacement body becomes difficult for some reason and the operator forcibly rotates the rotary roller, the engaged state of the second body and the first body is released and the second body is relatively moved, thus preventing movement of the first body in the axial direction. | 2014-11-20 |
20140343661 | PROCESS FOR MEDICAL COMPONENTS AND USES THEREOF - The invention relates to a process for making a medical component such as a medical implant for example a graft or stent-graft, said medical component comprising ultra high molecular weight polyethylene (UHMWPE) fibers, a medical component obtainable by said process as well as uses of said process and medical component. | 2014-11-20 |
20140343662 | Method and Device for Producing a Bioartificial Tissue Construct - The tissue construct with viable cells in an extracellular matrix made of fibrin is produced with a special method, in which a matrix material and cells are shaped into a hollow body, in particular a tubular hollow body, by means of a rotational casting method in a hollow mould ( | 2014-11-20 |
20140343663 | DEVICES AND METHODS FOR ASSISTING MEDICAL TREATMENTS - An intravascular device ( | 2014-11-20 |
20140343664 | IMPLANTABLE FLOW DIVERTER - A flow diverter for implantation into a patient's vessel includes a distal annular support element and a proximal annular support element, the proximal and distal support elements supporting a longitudinally twisted diverter element. The flow diverter is designed to be disposed within a vessel and to impart a rotational or twisting motion to the flow of blood passing therethrough, thereby to reduce the pressure of blood at the center of the vessel. Such flow diversion can reduce the pressure of blood impinging upon an aneurysm at a bifurcation downstream of the vessel. The device can be particularly useful for the treatment of aneurysms occurring at the bifurcation between the basilar artery and the posterior cerebral arteries. | 2014-11-20 |
20140343665 | STENT FOR THE POSITIONING AND ANCHORING OF A VALVULAR PROSTHESIS IN AN IMPLANTATION SITE IN THE HEART OF A PATIENT - The present invention relates to a stent for the positioning and anchoring of a valvular prosthesis in an implantation site in the heart of a patient. Specifically, the present invention relates to an expandable stent for an endoprosthesis used in the treatment of a narrowing of a cardiac valve and/or a cardiac valve insufficiency. So as to ensure that no longitudinal displacement of a valvular prosthesis fastened to a stent will occur relative the stent in the implanted state of the stent, even given the peristaltic motion of the heart, the stent according to the invention comprises at least one fastening portion via which the valvular prosthesis is connectable to the stent. The stent further comprises positioning arches and retaining arches, whereby at least one positioning arch is connected to at least one retaining arch. | 2014-11-20 |
20140343666 | STENT FOR BIFURCATED VESSEL - A stent for a bifurcated vessel includes a stent body ( | 2014-11-20 |
20140343667 | BIOABSORBABLE BIOMEDICAL IMPLANTS - A bioabsorbable biomedical implant is disclosed. The implant includes a tubular scaffold comprising a plurality of interconnected polymer struts. The interconnected polymer struts defines a plurality of deformable cells. The polymer struts have an average thickness of no more than 150 μm. Methods for making the bioabsorbable biomedical implant, including the methods for making the fiber-reinforced polymer composite materials for the tubular scaffold, are also disclosed. | 2014-11-20 |
20140343668 | ANNULOPLASTY RING WITH INTRA-RING ANCHORING - Apparatus is provided that includes an annuloplasty system for use on a subject. The system includes an annuloplasty ring, which includes a sleeve having a lumen, and at least one anchor, shaped so as to define a coupling head and a tissue coupling element, which tissue coupling element is shaped so as to define a longitudinal axis, and is configured to penetrate cardiac tissue of the subject in a direction parallel to the longitudinal axis. The system further includes an anchor deployment manipulator, configured to be removably positioned within the lumen of the sleeve, and, while so positioned, to deploy the tissue coupling element from a distal end of the deployment manipulator through a wall of the sleeve into the cardiac tissue in the direction parallel to the longitudinal axis of the tissue coupling element and parallel to a central longitudinal axis through the distal end of the deployment manipulator. | 2014-11-20 |
20140343669 | METHODS AND APPARATUS FOR DELIVERING A PROSTHETIC VALVE TO A BEATING HEART - A method for delivering a prosthetic valve to a patient's heart having a native valve with a plurality of valve leaflets includes providing a delivery device with a prosthetic valve, advancing the delivery device toward the native valve, and expanding a portion of the prosthetic valve to form a flanged region that is upstream of the valve leaflets. One or more tabs on the prosthetic valve are released so that they expand outward to a position that is transverse to the longitudinal axis of the prosthetic valve. The position of the prosthetic valve is adjusted relative to the valve leaflets and rapid pacing is applied to the patient's heart so that the valve leaflets move inward toward the prosthetic valve or the delivery device. The tabs are further released to allow the tabs to move into their final positions. | 2014-11-20 |
20140343670 | PROSTHETIC HEART VALVE DELIVERY APPARATUS - Certain embodiments of the present disclosure provide a prosthetic valve (e.g., prosthetic heart valve) and a valve delivery apparatus for delivery of the prosthetic valve to a native valve site via the human vasculature. The delivery apparatus is particularly suited for advancing a prosthetic heart valve through the aorta (i.e., in a retrograde approach) for replacing a diseased native aortic valve. The delivery apparatus in particular embodiments is configured to deploy a prosthetic valve from a delivery sheath in a precise and controlled manner at the target location within the body. | 2014-11-20 |
20140343671 | PERIVALVULAR SEALING FOR TRANSCATHETER HEART VALVE - The present disclosure is directed to embodiments of catheter-based prosthetic heart valves, and in particular, prosthetic heart valves having sealing devices configured to seal the interface between the prosthetic valve and the surrounding tissue of the native annulus in which the prosthetic valve is implanted. In one embodiment, a prosthetic heart valve includes an annular sealing member that can be placed in a delivery orientation extending axially away from one end of the valve when the valve is in a radially compressed state. When the valve is expanded, the expansion of the frame causes the sealing member to be pulled to an operative orientation covering a portion of the frame. The present disclosure also discloses new mechanisms and techniques for mounting valve leaflets to a frame of a prosthetic heart valve. | 2014-11-20 |
20140343672 | ARTIFICIAL HEART - An artificial heart, comprising an energy storage device, an actuator device and two pumping chambers, each with an inlet opening and an outlet opening, wherein each pumping chamber is bounded by at least one flexible wall and one rigid wall and the volume of each pumping chamber can is variable by deformation of the flexible wall by means of the actuator device, whereby the flexible wall, starting from a suction position in which the volume of the respective pumping chamber is at a maximum, can be converted to a pumping position in which the volume of the feed chamber is at a minimum by means of the actuator device, wherein the inlet opening and the outlet opening of each pumping chamber each have a non-return valve and the non-return valves can be reciprocally in an opened and a closed position, wherein the actuator device is located between the pumping chambers. | 2014-11-20 |
20140343673 | Extracellular Matrix Encasement Structures and Methods - A remodelable encasement structure comprising a pouch formed from at least one sheet of bioremodelable material, the pouch including an internal region and at least one lead conduit, the internal region being configured to receive a device therein, the lead conduit being configures to receive at least one device lead therein, the bioremodelable material comprising an extracellular matrix (ECM) composition that includes an ECM component derived from a mammalian source. | 2014-11-20 |
20140343674 | PROSTHETIC ELEMENT FOR CONNECTING THE STAPES FOOTPLATE TO A MIDDLE EAR OSSICULAR PROSTHESIS - A prosthetic element enables the stapes footplate to be connected to the foot of a middle ear ossicular prosthesis. The prosthetic connection element is of biocompatible material and forms part of the foot or is connected or connectable to this latter, and includes a body provided with a flat surface intended to rest on the footplate and having an area sufficient to prevent reabsorption of the footplate osseous tissue as a result of the pressure which the ossicular prosthesis exerts on the footplate. The prosthetic element includes at least two pointed projections projecting from the flat surface and intended to penetrate the footplate. | 2014-11-20 |
20140343675 | Balloon Implant Device - A shoulder implant device includes one or more fixation features including an acromial intrusion element and an inflatable humeral balloon portion that receives a fluid through the acromial intrusion element. The intrusion element comprises a valve that can receive multiple needle sticks to add or remove fluid to or from the inflatable humeral balloon. The device is implanted in a subacromial space such that the one or more fixation features at least secure the device to the acromion and the inflatable balloon portion rests against the proximal end of the corresponding humerus. Fluid in the balloon portion maintains separation of the acromion and the humerus to reduce or prevent impingement. | 2014-11-20 |
20140343676 | Skin Substitute and Wound Dressing with Variable Pore Sizes - An improved skin substitute is presented comprised of a silicone layer backed up with a woven nylon fabric layer, the silicone layer possessing a regular pattern of slits that permit the porosity of the skin substitute to be adjusted by clinicians by means of applying tension to the skin substitute that differentially opens the slits. A variety of therapeutic substances can be applied to the skin substitute to promote healing, including aloe and other medicinal preparations. | 2014-11-20 |
20140343677 | Intervertebral devices and related methods - Intervertebral devices and systems, and methods of their use, are disclosed having configurations suitable for placement between two adjacent vertebrae, replacing the functionality of the disc therebetween. Intervertebral devices and systems contemplated herein are implantable devices intended for replacement of a vertebral disc, which may have deteriorated due to disease for example. The intervertebral devices and systems are configured to allow for ample placement of therapeutic agents therein, including bone growth enhancement material, which may lead to better fusion between adjacent vertebral bones. The intervertebral devices and systems are configured for use in minimally invasive procedures, if desired. | 2014-11-20 |
20140343678 | Adjustable Implant and Insertion Tool - An adjustable spinal implant includes a lower body, an upper body, a locking pawl, and a locking key. The upper body and the lower body are pivotable relative to one another between a collapsed position and an expanded position. The upper body includes a locking flange that extends towards the lower body. The locking pawl is coupled to the lower body and is moveable between a locked position such that the upper and lower bodies are fixed relative to the one another and an unlocked position such that the upper and lower bodies are moveable relative to one another. The locking key is moveable between a locked state such that the locking pawl is fixed in the locked position and an unlocked state wherein the locking pawl is moveable between the locked position and the unlocked position. | 2014-11-20 |
20140343679 | DISC-FACET VERTEBRAL DEVICE - This prosthesis ( | 2014-11-20 |
20140343680 | BONE PREPARATION TOOL KIT AND ASSOCIATED METHOD - A prosthesis ( | 2014-11-20 |
20140343681 | UNICONDYLAR TIBIAL KNEE IMPLANT - An implant providing for both short and long term stability and fixation is disclosed. The implant includes a plurality of projections extending from a bone contacting surface, and a porous material covering at least portions of the surface and projections. The orientation of the projections and the porous material provide for the stability and fixation. Methods of forming and utilizing the implant are also disclosed. | 2014-11-20 |
20140343682 | CONVERTIBLE ACETABULAR BEARING - An acetabular bearing is configured to be convertible between direct connection with the acetabulum of a patient's hip, and connection to an acetabular cup shell or other mounting structure, which is configured to be connected to the acetabulum. | 2014-11-20 |
20140343683 | MEDICAL STENT HAVING MOVEMENT PREVENTION MEANS - The present invention provides a medical stent with a stopper which can be inserted into lumens of a human such as the duodenum, the colon, the biliary tract, and the esophagus, and that is useful for lesions due to stricture caused by benign and malignant tumors. | 2014-11-20 |
20140343684 | CATHETER OR STENT DELIVERY SYSTEM - A method for delivering catheters, and stents composed of soft, compliant polymers through anatomical passages. These devices have a bulbous anchorage end with a diameter greater than the rest of the catheter. To facilitate implant and delivery a pusher catheter or sheath with an internal lumen larger than the outer diameter of the catheter but smaller than the outer diameter of the bulbous anchorage end. The distal end of pusher catheter or the sheath physically engages the proximal end of the bulbous anchorage end and applies an axial force to coaxially advance the catheter over a guidewire though anatomical passages. This method allows a physician to move the catheter to an anatomical site without the device exhibiting buckling due to axial force applied. Similarly, this delivery method will allow more force to be applied to the distal end of the catheter diminishing the likelihood of buckling. | 2014-11-20 |
20140343685 | FEMORAL COMPONENT FOR A HIP PROSTHESIS - A femoral component for a hip prosthesis has a proximal end for disposition at a superior position in a femur and a distal end opposite the proximal end. The femoral component has opposite medial and lateral sides and opposite anterior and posterior faces extending between the medial and lateral sides. At least a proximal part of the femoral component has a first superior-to-inferior taper so that a medial to lateral dimension decreases gradually from the proximal end toward the distal end, a second superior-to-inferior taper so that an anterior to posterior dimension of the femoral component decreases gradually from the proximal end toward the distal end and a lateral-to-medial taper so that an anterior to posterior dimension of the femoral component decreases gradually from the lateral side toward the medial side. | 2014-11-20 |
20140343686 | ORTHOPEDIC AUGMENTS HAVING RECESSED POCKETS - Systems, devices, and methods are described for providing orthopedic augments having recessed pockets that receive a fixation material. The orthopedic augments include an outer surface that interfaces with a patient's tissue or bone, and an inner surface that interfaces with an implant, the inner surface comprising a recessed pocket configured to receive a fixation material, a rim around at least a portion of the recessed pocket, and a port in the rim, wherein the recessed pocket extends along the inner surface in at least a direction laterally from the port. | 2014-11-20 |
20140343687 | Substrate with a Structured Surface and Methods for the Production Thereof, and Methods for Determining the Wetting Properties Thereof - An implant includes a microstructured hyperhydrophilic surface with protrusions and depressions in which a spacing between the protrusions as a statistical mean is in a range of 1 to 100 μm and a profile height of the protrusions and depressions as a statistical mean is in the range of 1 to 80 μm. | 2014-11-20 |
20140343688 | LAMINATED TISSUE GRAFTS COMPOSED OF WHARTON'S JELLY AND METHODS OF MAKING AND USING THE SAME - Described herein are tissue grafts derived from the placenta with improved physical and biological properties. In one aspect, the tissue graft includes a first membrane comprising Wharton's jelly laminated with amnion, chorion, or a combination thereof. The presence of Wharton's jelly in the grafts enhances the performance of allograft amniotic-derived, caderivic allograft, xenograft, or alloplast soft tissue substitutes. | 2014-11-20 |
20140343689 | SYSTEM AND METHOD FOR PERCUTANEOUSLY ADMINISTERING REDUCED PRESSURE TREATMENT USING A FLOWABLE MANIFOLD - A reduced pressure delivery system for applying a reduced pressure to a tissue site includes a manifold delivery tube having a passageway and a distal end, the distal end configured to be percutaneously inserted and placed adjacent the tissue site. A flowable material is provided and is percutaneously deliverable through the manifold delivery tube to the tissue site. The flowable material is capable of filling a void adjacent the tissue site to create a manifold having a plurality of flow channels in fluid communication with the tissue site. A reduced pressure delivery tube is provided that is capable of fluid communication with the flow channels of the manifold. | 2014-11-20 |