38th week of 2013 patent applcation highlights part 65 |
Patent application number | Title | Published |
20130245693 | VERTEBRAL FACET JOINT PROSTHESIS AND METHOD OF FIXATION - Devices and methods for altering the spacing and motion at the facet joints of the vertebral column are provided. One embodiment of the invention comprises a prosthesis with surfaces configured to articulate with the facets of the facet joint. A retaining member for anchoring the prosthesis within the facet joint is optionally included. Methods for surgically and less invasively implanting the prosthesis and securing the prosthesis to the articular processes or surrounding soft tissue are also provided. | 2013-09-19 |
20130245694 | APPARATUS AND METHOD FOR DIRECT VERTEBRAL ROTATION - An instrument for spinal rotation that aligns and holds direct vertebral rotation (DVR) lever arms relative to each other to achieve an initial axial alignment of a segment of vertebrae and allows the final DVR rotation by rotating the instrument and lever arms together. A method of direct vertebral rotation that allows rotating the vertebrae to be aligned relative to each other, and collectively rotating the vertebrae to be aligned relative to adjacent spinal segments by rotating the direct vertebral rotation instrument. A system for direct vertebral rotation having at least two pedicle screws. The system also includes at least two levers attachable to the pedicle screws and a clamping instrument configured to clamp the levers. | 2013-09-19 |
20130245695 | VETERINARY PLATE - A bone fixation device includes a plate body which includes (a) a first body portion lying in a first plane, (b) a second body portion lying in a second plane and (c) an interface body portion lying in a third plane. The first plane is angled relative to the second plane and the third plane is angled relative to the first and second planes. A longitudinal axis of the first body portion is angled with respect to a longitudinal axis of the second body portion. The first body portion has first and second openings extending therethrough. The second body portion has third and fourth openings extending therethrough. | 2013-09-19 |
20130245696 | SYSTEM FOR TREATING BONE FRACTURES - An ulnar fixation plate includes a head portion configured to conform to a volar side of an ulnar bone proximate to an ulnar head, the head comprising of first head portion configured to receive a first fixation device, a second head portion configured to receive a second fixation device, and a shaft portion coupled to the head portion with the shaft portion configured to conform to the volar side of the ulnar bone. | 2013-09-19 |
20130245697 | DYNAMIC BONE FIXATION ELEMENT - A dynamic bone fixation element can include a sleeve elongate along a first direction and a fixation member. The sleeve can define a channel that extends from a proximal end through to a distal end along the first direction. The channel has a first cross-sectional dimension. The fixation member has a head, a shaft extending from the head and elongate along a second direction, and an abutment member extending from the shaft and integral with the shaft, wherein the shaft extends through the channel such that the sleeve is captured between the abutment member and the head. At least a portion of the shaft that is within the channel has a second cross-sectional dimension that is less than the first cross-sectional dimension such that the fixation member is moveable with respect to the sleeve along a direction that has a directional component transverse to the first direction. | 2013-09-19 |
20130245698 | CRANIOTOMY CLOSURES - Craniotomy closures comprising surgical fasteners are described for use in reattaching a skull flap removed from the skull of a patient during brain surgery. Methods of using the same are also described. Surgical strips used in combination with the fasteners are shaped to follow the perimeter contour of the skull flap. The craniotomy closures are designed to encourage bone growth and healing of the skull flap and they can be used to deliver medication and bone growth enhancement materials to the surgical site. | 2013-09-19 |
20130245699 | FRACTURE FIXATION PLATE, SYSTEM AND METHODS OF USE - A plate for fracture fixation, a system and methods are provided including a plurality of individually adjustable heads and various features and accessories to achieve: a.) superior fixation of the plate to osteoporotic diaphyseal bone; b.) improved visualization of the fracture line; c.) intraoperative adjustability to achieve better contact of the plate and the bone; d.) reduced risk of post-surgery tendon rupture; d.) improved fixation of small volar marginal fragments; e.) improved targeting and fixing of particular fractured bone fragments and, f.) reduced surgical operation time. | 2013-09-19 |
20130245700 | CMC REPAIR USING SUTURE-BUTTON CONSTRUCT - A button and attached suture loop for CMC repair. A suture strand is threaded through holes in the button to attach the button to the suture. The suture ends are then brought together (by being swaged, spliced or cinched together, for example) to form the suture loop comprising a continuous, uninterrupted suture loop with a single strand of swaged-together ends. The swaged-together ends are attached to a suture passing instrument such as a K-wire (Kirschner wire) that is also used to drill a hole through adjoining metacarpals (for example, the first and second metacarpals). The swaged-together ends of the suture are then passed through the drill holes in the first and second metacarpals, and the ends of the suture are pulled until the button abuts one of the first and second metacarpals. A second button is used to secure the cut suture ends to the other metacarpal. | 2013-09-19 |
20130245701 | ANCHORING SYSTEMS AND METHODS FOR SURGERY - A surgical ring and related methods for plantar plate reconstruction and other surgical procedures are described. In particular, the described anchoring systems and surgical methods may include an anchor configured to wrap at least partially around a first bone associated with an affected joint, and wrap at least partially around a tissue alongside the first bone. The anchor may be compressed in a number of ways so as to compress the tissue alongside the first bone against the first bone. The anchor may be formed from a compressible material, configured with an open shape, and/or or include mechanically closeable or compressible features, and the like. The anchor may be formed from various materials including non-bioabsorbable, bioabsorbable, and/or superelastic materials. The first bone may be a metatarsal or phalanx and the tissue alongside the first bone may be a ligament, a plantar plate, or similar tissue. | 2013-09-19 |
20130245702 | SPINAL IMPLANT SYSTEM AND METHOD - A spinal implant system includes a first member comprising walls that include a first end surface defining a first locking cavity, a second end surface and an outer surface extending therebetween. A second member includes a first arm having an inner surface that defines a first cavity and a second arm having an inner surface that defines a second cavity. The inner surface of the first arm includes a first projection disposable in the first cavity and the inner surface of the second arm includes a second projection disposable in the second cavity. A third member includes a first extension having an inner surface that defines a first cavity and a second extension having an inner surface that defines a second cavity. The third member is configured for axial translation relative to the second member between a first orientation and a second orientation. Methods of use are disclosed. | 2013-09-19 |
20130245703 | METHOD AND APPARATUS FOR SACROILIAC JOINT FIXATION - Disclosed is a fixation device for sacroiliac joint stabilization. The fixation device includes an elongated body comprising a bone anchor at a distal end. An axially moveable proximal anchor is carried by the proximal end of the fixation device. In one embodiment, the device is inserted through the ilium of the pelvis and the bone anchor is rotated into position within the sacrum. The proximal anchor is distally advanced with respect to the bone anchor to provide compression across the sacroiliac joint. | 2013-09-19 |
20130245704 | SURGICAL SYSTEM INCLUDING POWERED ROTARY-TYPE HANDPIECE - A surgical system which may include a controller, a data entry device, a powered surgical handpiece and a surgical tool adapted to couple to the surgical handpiece. The surgical handpiece can include motor direction control and feedback, safety stop features, stimulation and nerve integrity monitoring, a tool connector assembly configured to retain a variety of surgical tools and optional navigation and/or electric ratcheting features. | 2013-09-19 |
20130245705 | SPINAL IMPLANT SYSTEM AND METHOD - An extender includes a first arm defining a first longitudinal axis and including a first extension and a second extension. The first extension includes an outer surface and a projection extending from the outer surface, the projection including a ramp and a first locking element. The first extension includes an inner surface defining a longitudinal cavity. The projection is transversely moveable between a first configuration such that the projection extends beyond the outer surface and a second configuration whereby the second extension axially translates within the longitudinal cavity and engages the ramp such that the projection is disposed in alignment with the outer surface and the first locking element engages an implant. Methods of use are disclosed. | 2013-09-19 |
20130245706 | GUIDEWIRE HAVING A DISTAL FIXATION MEMBER FOR DELIVERING AND POSITIONING SHEET-LIKE MATERIALS IN SURGERY - A guidewire for use with an implant delivery system in delivering a sheet-like implant is disclosed. The guidewire can include a distal tissue fixation member for releasable connection to a first location proximate a treatment site. An implant delivery system can include a distal guidewire port for receiving the proximal end of the guidewire. The implant delivery system is tracked over the guidewire to a selected position defined by the guidewire attachment. The tissue fixation member includes means for temporarily or reversibly fixing the distal end of the guidewire to tissue, such as bone. The means for affixing can include a K-wire, a screw, a pin or other fixation member. | 2013-09-19 |
20130245707 | ANATOMICAL LOCATION MARKERS AND METHODS OF USE IN POSITIONING SHEET-LIKE MATERIALS DURING SURGERY - A tissue marker assembly which can be useful with an implant delivery system for delivering a sheet-like implant is disclosed. The tissue marker assembly can include a delivery sleeve with a tissue marker slidably disposed within a lumen therethrough. A proximal handle can be coupled to the tissue marker and delivery sleeve, having a first part and a second part. The second part of the proximal handle can be releasably attached to the tissue marker proximal end so that the second part can be removed to allow the delivery sleeve to be removed proximally over the tissue marker after it is affixed to tissue. The distal portion of the marker can include a plurality of longitudinally extending arms when unconstrained project outward from the shaft to retain the marker's position in tissue. | 2013-09-19 |
20130245708 | EXTERNAL DEFIBRILLATOR - An external defibrillator includes patient electrodes ( | 2013-09-19 |
20130245709 | DYNAMIC MORPHOLOGY BASED ATRIAL AUTOMATIC THRESHOLD - Methods and systems for performing capture threshold tests are described. During an initialization procedure a capture detection interval and capture detection threshold are determined based on peak values of cardiac signals sensed following the supracapture threshold initialization pulses. Following initialization, a plurality of pacing pulses to the atrium are delivered and the peak values of the cardiac signals sensed following each of the plurality of pacing pulses are determined. The peak values are compared to the pacing artifact threshold and the capture detection threshold. A timing of each of the peak values is compared to the capture detection interval. For each pacing pulse, discrimination between a captured response, a noncaptured response, and a fusion response is based on the peak value and timing comparisons. | 2013-09-19 |
20130245710 | INTEGRAL STIMULATION LEAD - An apparatus, such as included as a portion of cardiac rhythm management (CRM) system, can include a subcutaneously-implantable medical device. The subcutaneously-implantable medical device can include a header assembly including a stylet access port, and the apparatus can include an intravascularly-deliverable lead assembly permanently attached to the header assembly and including a lumen to receive a stylet via the stylet access port included in the header assembly. | 2013-09-19 |
20130245711 | NON-INVASIVE VAGAL NERVE STIMULATION TO TREAT DISORDERS - Devices, systems and methods are disclosed for treating a variety of diseases and disorders that are primarily or at least partially driven by an imbalance in neurotransmitters in the brain, such as asthma, COPD, depression, anxiety, epilepsy, fibromyalgia, and the like. The invention involves the use of an energy source comprising magnetic and/or electrical energy that is transmitted non-invasively to, or in close proximity to, a selected nerve to temporarily stimulate, block and/or modulate the signals in the selected nerve such that neural pathways are activated to release inhibitory neurotransmitters in the patient's brain. | 2013-09-19 |
20130245712 | NON-INVASIVE VAGAL NERVE STIMULATION TO TREAT DISORDERS - Devices, systems and methods are disclosed for treating bronchial constriction related to asthma, anaphylaxis, chronic obstructive pulmonary disease (COPD), exercise-induced bronchospasm and post-operative bronchospasm. The treatment comprises transmitting impulses of energy non-invasively to selected nerve fibers that activate neural pathways to reduce the release of acetycholine from airway-related vagal preganglionic neurons within the brain of the patient. The transmitted energy impulses, comprising magnetic and/or electrical energy, stimulate the selected nerve fibers to produce the bronchodilation. | 2013-09-19 |
20130245713 | DEVICE FOR THE DESYNCHRONIZATION OF NEURONAL BRAIN ACTIVITY - A device for desynchronizing neuronal brain activity involving a neuron population firing in a synchronized manner at a pathological frequency. The device includes an electrode configured to generate stimuli that stimulate the neuron population; and a control unit configured to control the electrode to generate the stimuli in sequence, wherein the stimuli succeed each other with a predetermined frequency f. The predetermined frequency f is substantially equal to g×n/m, where g is the pathological frequency, and n and m are integers. | 2013-09-19 |
20130245714 | Method and Apparatus for Event-Triggered Reinforcement of a Favorable Brain State - Methods and apparatuses are disclosed for potentiating a favorable brain state that is associated with relief in symptoms of a brain condition. Techniques include monitoring one or more brain signals and detecting an episode of a favorable brain state based on the one or more brain signals, the favorable brain state associated with a decrease in one or more symptoms of a brain condition of the patient. Then, in response to the detection of the favorable brain state episode, electrical stimulation that potentiates the favorable brain state is delivered to the brain of the patient, the electrical stimulation delivered within a window of time opened for detection of each favorable brain state episode. | 2013-09-19 |
20130245715 | FIELD AUGMENTED CURRENT STEERING USING VOLTAGE SOURCES - A neurostimulation comprises a plurality of electrical terminals configured for being respectively coupled to an array of electrodes, at least three configurable sources respectively coupled to at least three of the electrical terminals, and control circuitry configured for programming each of the at least three configurable sources to be either a current source or a voltage source. A method of providing neurostimulation therapy to a patient using an array of electrodes implanted adjacent neural tissue of the patient, comprises conveying electrical stimulation energy between a first one the electrodes and a second one of the electrodes, thereby creating an electrical field potential within the neural tissue, regulating a first current flowing through the first electrode, and regulating a first voltage at a third different one of the electrodes, thereby modifying a shape of the electrical field potential within the neural tissue. | 2013-09-19 |
20130245716 | SLEEVE FOR STIMULATION OF TISSUE REGENERATION - The regenerative sleeve encompasses the wound site of an amputated appendage and provides an environment conducive to tissue regeneration. The sleeve includes a tubular reservoir having an outer body that encloses the end of the appendage including the wound site and provides a sealed wound space between the wound site and the outer body. The sleeve also includes a cuff disposed in an opening formed in the outer body, the cuff being configured to fit on the appendage, and an access port disposed on the outer body and configured to allow administration of fluids to the wound space. The sleeve assembly was effective in supporting early stages of murine digit tip regeneration when combined with a porcine urinary bladder matrix (UBM) pepsin digest and electrical stimulation. | 2013-09-19 |
20130245717 | Using Alternative Stimulus Waveforms To Improve Pitch Percepts Elicited With Cochlear Implant Systems - A cochlear implant system is described which includes an electrode array for implantation in the scala tympani of a cochlea. Electrodes on the outer surface of the electrode array apply electrode stimulation signals to nearby neural tissue. An implantable stimulator module develops the electrode stimulation signals. The electrode stimulation signals have different waveforms. A basal waveform for one or more electrodes at the basal end of the electrode array has the form of a sequence of conventional high-amplitude short-duration electrode stimulation signals. An apical waveform for one or more electrodes at the apical end of the electrode array has the form of a sequence of lower-amplitude longer-duration electrode stimulation signals. The apical waveform is adapted to selectively stimulate peripheral neural processes towards the apical end of the electrode array so as to provide a tonotopic place-pitch response to the electrode stimulation signals. | 2013-09-19 |
20130245718 | SYSTEMS AND METHODS FOR MONITORING NEUROSTIMULATION DOSING - Various implantable device embodiments may comprise a neural stimulator configured to deliver a neurostimulation therapy with stimulation ON times and stimulation OFF times where a dose of the neurostimulation therapy is provided by a number of neurostimulation pulses over a period of time. The neural stimulator may be configured to monitor the dose of the delivered neurostimulation therapy against dosing parameters. The neural stimulator may be configured to declare a fault if the monitored dose does not favorably compare to a desired dose for the neurostimulation therapy, or may be configured to record data for the monitored dose of the delivered neurostimulation therapy, or may be configured to both record data for the monitored dose of the delivered neurostimulation therapy and declare a fault if the monitored dose does not favorably compare to a desired dose for the neurostimulation therapy. | 2013-09-19 |
20130245719 | SYSTEM AND METHOD FOR ESTIMATING LOCATION AND DEPTH OF STIMULATION LEADS - A method and external control device for performing a medical procedure on a patient in which at least one stimulation lead is implanted. An electrical signal is conveyed from the stimulation lead into tissue of the patient. An electrical parameter indicative of tissue impedance is measured in response to the conveyance of the electrical signal. One of a plurality of different anatomical regions in which the stimulation lead is implanted is selected and/or a depth in which the stimulation is implanted is determined based on the measured electrical parameter. A stimulation parameter is defined based on the selected one anatomical region and/or implantation depth. Electrical stimulation energy from the stimulation lead is conveyed into the one determined anatomical region in accordance with the defined stimulation parameter. | 2013-09-19 |
20130245720 | Using the Case of an Implantable Medical Device to Broaden Communication Bandwidth - An improved implantable pulse generator (IPG) containing improved telemetry circuitry is disclosed. The IPG includes a telemetry coil within the conductive IPG case, not in the non-conductive header as is typical, which simplifies IPG design. The improved resonant circuit of which the coil is a part does not include a discrete tuning resistor with the coil, which tuning resistor was traditionally used to increase communication bandwidth of the coil to render it suitable for FSK telemetry. In lieu of the tuning resistor, the coil is intentionally inductively coupled to the case by positioning the coil a certain distance away from the case. Such coupling decreases the effective inductance and increases the effective series resistance in the improved resonant circuit, both of which increase the communication bandwidth. As such, suitable FSK telemetry can be achieved, even though the improved resonant circuit without the case would not on its own have suitable bandwidth. | 2013-09-19 |
20130245721 | External Controller/Charger System for an Implantable Medical Device Capable of Automatically Providing Data Telemetry Through a Charging Coil During a Charging Session - An external controller/charger system for an implantable medical device is disclosed, in which the external controller/charger system provides automatic switching between telemetry and charging without any manual intervention by the patient. The external controller/charger system includes an external controller which houses a telemetry coil and an external charging coil coupled to the external controller. Normally, a charging session is carried out using the external charging coil, and a telemetry session is carried out using the telemetry coil. However, when a patient requests to carry out telemetry during a charging session, the external charging coil is used instead of the internal telemetry coil. | 2013-09-19 |
20130245722 | SYSTEMS AND METHODS FOR MONITORING FOR NERVE DAMAGE - Various device embodiments may comprise an implantable medical device for implantation in a body and for applying neural stimulation to a neural target in the body. The device may comprise a neural stimulation electrode configured for use in stimulating the neural target, a neural stimulator configured to deliver neural stimulation through the electrode to the neural target, a sensor configured to sense a physiological response to stimulation of motor fibers at the neural target, and a controller operatively connected to the neural stimulator to control the neural stimulation and operatively connected to the sensor to receive a signal indicative of the physiological response. The controller may be configured to detect a potential neural injury and perform an action in response to the detected potential neural injury. | 2013-09-19 |
20130245723 | NEUROSTIMULATION SYSTEM FOR PREVENTING MAGNETICALLY INDUCED CURRENTS IN ELECTRONIC CIRCUITRY - A neurostimulation device capable of being placed between an active stimulation state and an inactive stimulation state and method of using same. The neurostimulation device comprises a plurality of electrical terminals configured for being respectively coupled to a plurality of stimulation electrodes, a first solid-state switching device coupled to a first one of the electrical terminals, a variable power source coupled to the first switching device, and a controller configured for, when the neurostimulation device is in the inactive stimulation state, prompting the variable power source to selectively output a relatively low voltage to place the first switching device into a first open state and a relatively high voltage to place the first switching device into a second open state. | 2013-09-19 |
20130245724 | SYSTEM AND METHOD FOR FACILITATING PHOTOTHERAPEUTIC TREATMENT - A phototherapeutic device comprises a system for facilitating phototherapeutic treatment. The system comprises an input device configured to receive input from a user. The system further comprises a display device configured to communicate information to the user. The system further comprises a controller. The controller is configured to receive user identification data from the input device. The controller is further configured to retrieve treatment history based on the user identification data. The controller is further configured to retrieve a treatment protocol based on the user identification data. The controller is further configured to generate a suggested treatment based on the retrieved treatment history and the retrieved treatment protocol. The controller is further configured to communicate the suggested treatment to the display device. | 2013-09-19 |
20130245725 | APPARATUS AND METHODS FOR OPTICAL STIMULATION OF NEURAL TISSUES - An apparatus for stimulating a neural tissue of a living subject. The neural tissue is characterized with a thermal diffusion time, T | 2013-09-19 |
20130245726 | Methods and Apparatus for Multi-Vessel Renal Neuromodulation - Methods and apparatus are provided for multi-vessel neuromodulation, e.g., via a pulsed electric field. Such multi-vessel neuromodulation may effectuate irreversible electroporation or electrofusion, necrosis and/or inducement of apoptosis, alteration of gene expression, action potential attenuation or blockade, changes in cytokine up-regulation and other conditions in target neural fibers. In some embodiments, the multi-vessel neuromodulation is applied to neural fibers that contribute to renal function. Such multi-vessel neuromodulation optionally may be performed bilaterally. | 2013-09-19 |
20130245727 | SYSTEMS AND METHODS FOR THERMOLIPOLYSIS USING RF ENERGY - Disclosed herein are systems and methods for preferentially heating subcutaneous tissue. Systems for heating subcutaneous tissue may comprise one or more radio-frequency (RF) electrodes having contoured tissue contacting surfaces, such as electrodes with concave or convex surface contours. Methods may comprise applying RF voltage or current from one or both of the handpieces to attain a target tissue and/or electrode temperature and to maintain the tissue and/or electrode at that temperature. | 2013-09-19 |
20130245728 | VAGINAL REMODELING DEVICE AND METHOD - This invention provides devices and methods for remodeling the female genital tissue, the device comprising a treatment tip, wherein the distal end of the treatment tip is conical, spherical, hemispherical, oval or circular in shape. The device further comprises one or more energy delivery elements for simultaneous cooling of the vaginal epithelium and transmission of energy for heating the tissues underneath the epithelium. In one embodiment, said device may further comprise one or more of the following: one or more temperature sensors for measuring the temperature at or below the epithelium; one or more directional sensors mounted on the hand piece or treatment tip; and one or more depth markers to show the depth of penetration of the treatment tip into the vagina. In another embodiment, this invention provides a device having a finger holder with electrodes for remodeling the female genital tissue. | 2013-09-19 |
20130245729 | COLD THERAPY SYSTEMS AND METHODS - A cold therapy system including a cooling bath; a therapy pad in fluid communication with the cooling bath; a pump positioned and arranged to pump water from the cooling bath to the therapy pad and back to the cooling bath; and a control unit controlling the pump, the control unit programmed to operate the pump according to a cycle in which the pump is operated at less than maximum to cause the therapy pad temperature to be raised and to conserve a cooling resource within the cooling bath. | 2013-09-19 |
20130245730 | INFLATABLE CONVECTIVE PAD FOR SURGERY - An inflatable convective pad for warming a person during surgery has two ends, two sides, and at least two openings, each located in an area of the pad between the two ends and between a respective side and the center of the pad. The openings, which may be in the form of slits, allow the threading of a sheet or the person's arms through the pad to restrain the arms during surgery. | 2013-09-19 |
20130245731 | SYSTEMS AND METHODS WITH INTERRUPT/RESUME CAPABILITIES FOR TREATING SUBCUTANEOUS LIPID-RICH CELLS - Systems for removing heat from a subject's subcutaneous lipid-rich regions, such as tissue, organs, cells, and so forth, are described herein. In various embodiments, the system includes a treatment device and a controller for controlling a treatment process. The controller is configured to detect and compensate for an interruption in the treatment process. | 2013-09-19 |
20130245732 | LEAD HEADER AND MANUFACTURE THEREOF - A lead header for an implantable medical lead is in the form of a metal sheet bent to form a metal tube having a lumen. The metal sheet has a protruding portion that extends radially inwardly into the lumen. The protruding portion may be lip arranged in connection with one of the longitudinal sides of the metal sheet that is bent to protrude radially inwardly into the lumen, or it may be a dent formed in the metal sheet. In either case, the protruding portion is configured to transform a rotation of a helical fixation element of the medial lead that is at least partly present in the lumen into a longitudinal movement of the helical fixation element relative to the lead header. | 2013-09-19 |
20130245733 | INTEGRATED SWITCHING CIRCUIT AND PULSE GENERATOR IN A NEUROSTIMULATOR LEAD - A stimulation lead for connecting a pulse generator having a plurality of outputs to electrodes of an electrode array includes a flexible body and the electrode array. The electrode array is distal to the flexible body and the flexible body has a proximal portion and an interface portion. A selection circuit within the interface portion has a plurality of inputs, each input of the selection circuit connected to an output of the pulse generator and a plurality of outputs, each output of the selection circuit being coupled to a respective one of the electrodes of the electrode array. The plurality of outputs of the selection circuit are greater in number than the plurality of outputs of the pulse generator. | 2013-09-19 |
20130245734 | NEUROSTIMULATION LEAD DESIGN WITH VARYING RF IMPEDANCE FILARS - An implantable stimulation lead includes a lead body having a proximal end and a distal end; a plurality of electrodes disposed along the distal end of the lead body; a plurality of terminals disposed along the proximal end of the lead body, and a plurality of conductors disposed in the lead body and including a first conductor and a second conductor. Each conductor electrically couples at least one of the electrodes to at least one of the terminals. The first conductor has a RF impedance that is at least 25% greater in magnitude than the second conductor. | 2013-09-19 |
20130245735 | IMPLANTABLE MEDICAL ELECTRICAL LEAD AND CONNECTOR ASSEMBLY - An implantable system that includes a lead and an implantable signal generator wherein the plurality of electrical contacts and the plurality of insulating regions on the lead, and the plurality of electrical connectors and the plurality of electrical insulators in the connector block are configured so that each of the plurality of electrical contacts form operable connections to the electronic circuitry through each of the plurality of electrical connector, and the insulating regions and the electrical insulators electrically isolate adjacent operable connections. Leads, and methods are also disclosed. | 2013-09-19 |
20130245736 | IMPLANTABLE MEDICAL ELECTRICAL LEAD AND CONNECTOR ASSEMBLY - An implantable system that includes a lead and an implantable signal generator wherein the plurality of electrical contacts and the plurality of insulating regions on the lead, and the plurality of electrical connectors and the plurality of electrical insulators in the connector block are configured so that each of the plurality of electrical contacts form operable connections to the electronic circuitry through each of the plurality of electrical connector, and the insulating regions and the electrical insulators electrically isolate adjacent operable connections. Leads, and methods are also disclosed. | 2013-09-19 |
20130245737 | IMPLANTABLE MEDICAL LEAD HAVING REDUCED DIMENSION TUBING TRANSITION - Lead body designs for forming a fluid tight seal between a multilumen tube and other portions of a lead body are provided. One lead body design has a multilumen tube having a first portion defining a first number of lumens and a second reduced dimension portion defining a second number of lumens, the second number of lumens being smaller than the first number of lumens. The reduced dimension portion is attached to a distal tip portion of the lead body, forming a fluid tight passageway through the multilumen tube to the distal tip portion. Also provided are methods for forming such multilumen tubes and incorporating such multilumen tubes into a lead body. | 2013-09-19 |
20130245738 | ELECTRODE ARRAY WITH ELECTRODES HAVING CUTOUT PORTIONS AND METHODS OF MAKING THE SAME - A lead for brain stimulation includes a lead body having a distal end. At least one cable extends within the lead body, each cable comprising at least one conductor. The lead further includes a plurality of electrodes coupled to the at least one cable. Each of the plurality of electrodes defines a cutout portion that receives and attaches to a one of the at least one cable. | 2013-09-19 |
20130245739 | SELF-ANCHORED STIMULATOR LEAD AND METHOD OF INSERTION - An implantable electrical lead comprising an elongate lead body comprising first and second ends and an outer housing defining an interior channel. At least one electrical contact is positioned along the elongate lead body. An anchoring system is disposed at one end of the elongate lead body. The anchoring system is movable between an elongate configuration and a compressed configuration. The compressed configuration has a greater diameter than the elongate configuration. A linkage is provided having a first end attached to the anchoring system, an intermediate portion disposed within the interior channel of the elongate lead body, and a second end disposed outside of the elongate lead body adjacent to the second end of the elongate lead body. Movement of the linkage away from the elongate lead body moves the anchoring system from the elongate configuration to the compressed configuration. | 2013-09-19 |
20130245740 | Ear Implant Electrode and Method of Manufacture - A novel electrode array is described for ear implant systems such as cochlear implants (CI) and vestibular implants (VI). The electrode array includes electrode wires for carrying electrical stimulation signals. At a terminal end of each electrode wire is an electrode stimulation contact for applying the electrical stimulation signals to adjacent neural tissue. An electrode carrier of resilient material encases the electrode wires and has an outer surface with a plurality of contact openings exposing the stimulation contacts. Multiple bend control elements are distributed along the length of the electrode array to control bending flexibility of the electrode array as a function of a bend radius threshold to be greater for bending less than the bend radius threshold and lesser for bending greater than the bend radius threshold. | 2013-09-19 |
20130245741 | MRI-SAFE HIGH IMPEDANCE LEAD SYSTEMS - Some embodiments are directed to MRI/RF compatible medical interventional devices. A plurality of spaced apart high impedance circuit segments are configured to have a high Impedance at a high range of radiofrequencies and a low impedance at a low range of frequencies. The high impedance circuit segments may comprise co-wound coiled inductors and can reduce, block or inhibit RJ-transmission along the lead system ( | 2013-09-19 |
20130245742 | EXTERNAL STEERABLE FIBER FOR USE IN ENDOLUMINAL DEPLOYMENT OF EXPANDABLE DEVICES - The present disclosure describes treatment of the vasculature of a patient with an expandable implant. The implant is constrained to a reduced delivery diameter for delivery within the vasculature by at least one sleeve. The implant can be constrained to other diameters, such as an intermediate diameter. The sleeves can be expanded, allowing for expansion of the diameter of the expandable implant, by disengaging a coupling member from the sleeve or sleeves from outside of the body of the patient. The expandable implant can comprise a steering line or lines which facilitate bending and steering of the expandable implant through the vasculature of a patient. | 2013-09-19 |
20130245743 | SLEEVE RETRACTION SYSTEM - The present disclosure describes systems for endoluminal devices utilizing a sleeve for constraining an expandable device toward a constrained configuration suitable for endoluminal delivery to a treatment site along vasculature; and a mechanism for retracting at least a portion of the sleeve. | 2013-09-19 |
20130245744 | PROSTHESIS COMPRESSING ARRANGEMENT - A prosthesis | 2013-09-19 |
20130245745 | STENT AND STENT DELIVERY DEVICE - In one embodiment according to the present invention, a stent is described having a generally cylindrical body formed from a single woven nitinol wire. The distal and proximal ends of the stent include a plurality of loops, some of which include marker members used for visualizing the position of the stent. In another embodiment, the previously described stent includes an inner flow diverting layer. | 2013-09-19 |
20130245746 | BIOABSORBABLE STENT WITH TIME DEPENDENT STRUCTURE AND PROPERTIES AND REGIO-SELECTIVE DEGRADATION - A bioabsorbable polymeric stent with time dependent structure and properties and methods of treating a diseased blood vessel with the bioabsorable polymeric stent are disclosed. The structure and properties of the stent change with time and allow the vessel to be restored to a natural unstented state. The bioabsorbable stent loses mechanical integrity in a controlled manner due to modification of selected structural elements. | 2013-09-19 |
20130245747 | Anti-migration features and geometry for a shape memory polymer stent - A radially-expandable stent for implantation in a bodily passageway, being expandable from an initial unexpanded state to an expanded state, having an outer surface with a geometric pattern covering said outer surface to minimize migration after implantation is provided. Also provided is a method of manufacturing such a stent. | 2013-09-19 |
20130245748 | HELICAL HYBRID STENT - An expandable helical stent is provided, wherein the stent may be formed of an amorphous metal alloy or other non-amorphous metal with a securement. The stent is formed from flat or tubular metal in a helical coiled structure which has an undulating pattern. The main stent component may be formed of a single helically coiled component. Alternatively, a plurality of helically coiled ribbons may be used to form a stent heterogeneous in design, material, or other characteristic particular to that stent. The helical tubular structure may be secured with a securement, such as a weld, interlock or a polymer, to maintain the helical coils in a tubular configuration. The helical coils of the main stent component may be spaced apart or nestled to each other. The nestling of the undulation of adjacent helical coils contributes to maintaining the tubular shape of the helically coiled stent. In addition, the nestling of helical coils may prevent the polymer layer from sagging at any point between cycles of the helical coils. | 2013-09-19 |
20130245749 | Covered Stents with Degradable Barbs - The present invention is directed at a removable stent for providing reinforcement to a selected region of a selected body lumen including a resilient cylindrical layer, including at least one bioresorbable extrusion exterior from the resilient cylindrical layer for resisting migration of the removable stent when the removable stent is positioned in the selected region of the selected body lumen. The present invention also includes a temporary implantable endoprosthesis which includes a tubular, radially compressible and axially flexible structure, including at least one bioresorbable extrusion exterior from the resilient cylindrical layer for resisting migration of the removable stent when the removable stent is positioned in the selected region of the selected body lumen. | 2013-09-19 |
20130245750 | BIOMATERIALS WITH ENHANCED PROPERTIES AND DEVICES MADE THEREFROM - Biomaterials with enhanced properties such as improved strength, flexibility, durability and reduced thickness are useful in the fabrication of biomedical devices, particularly those subjected to continuous or non-continuous loads where repeated flexibility and long-term durability are required. These enhanced properties can be attributed to elevated levels of elastin, altered collagen types, and other biochemical changes which contribute to these enhanced properties. Examples of devices which would be improved by use of such tissue include heart valves, including percutaneous heart valves, and vascular grafts, patches and the like. Such enhanced materials can be sourced from specific populations of animals, such as neonatal calves, or in range-fed adult cattle, or can be fabricated or created from cell populations exhibiting such properties. In one embodiment, glutaraldehyde-fixed neonatal pericardial tissue is used to create leaflets in a percutaneous heart valve, and may be used without chemical fixation, with or without processes to remove residual cellular membranes, and utilized as a scaffold material for tissue engineering. | 2013-09-19 |
20130245751 | SYSTEMS AND METHODS FOR ENSURING SAFE AND RAPID DEPLOYMENT OF PROSTHETIC HEART VALVES - A quick-connect heart valve prosthesis that can be quickly and easily implanted during a surgical procedure is provided. The heart valve may include a substantially non-expandable, non-compressible prosthetic valve and a plastically-expandable frame, thereby enabling attachment to the annulus without sutures. A system and method for deployment includes an integrated handle shaft and balloon catheter. A safety member disposed between the balloon catheter and handle shaft prevents premature catheter advancement prior to heart valve placement at the annulus, and also may prevent premature balloon inflation prior to full catheter advancement. | 2013-09-19 |
20130245752 | DEVICE INTENDED TO BE ATTACHED TO OR INTERCONNECTED WITH A CATHETER, CATHETER AND METHOD - A device is intended to be attached to or interconnected with a medical implant, and intended to be attached to or interconnected with a catheter. The catheter is intended for implanting the implant. A catheter is suited for receiving at least one such device and a method provides a delivery implement with an implant detachably disposed in the device. | 2013-09-19 |
20130245753 | TWO-STAGE COLLAPSIBLE/EXPANDABLE PROSTHETIC HEART VALVES AND ANCHORING SYSTEMS - Prosthetic heart valve apparatus is adapted for delivery into a patient in a circumferentially collapsed condition, followed by circumferential re-expansion at the implant site in the patient. The apparatus includes an annular anchoring structure that can be implanted in the patient first. The apparatus further includes an annular valve support structure, which supports a flexible leaflet structure of the valve. The support and leaflet structures are initially separate from the anchoring structure, but they can be implanted in the patient by interengagement of the support structure with the already-implanted anchoring structure. | 2013-09-19 |
20130245754 | ADAPTIVE INTRAOCULAR LENS - An implantable ophthalmic device with flexible, fluid-filled membranes provide dynamically variable optical power to restore lost accommodation in individuals suffering from presbyopia or aphakia without moving parts or reducing the amount of transmitted light. Actuating the device causes the fluid-filled membrane to change curvature, which produces a corresponding change in optical power. For instance, squeezing the edge of the membrane causes the center of the membrane to bulge by an amount proportional to the squeezing force. Alternatively, heating or applying a voltage to the membrane may cause the liquid in the membrane to undergo a phase transition accompanied by a corresponding change in volume that causes the membrane to inflate so as to change the optical power of the device. | 2013-09-19 |
20130245755 | INSTALLATION AND SEALING OF A BATTERY ON A THIN GLASS WAFER TO SUPPLY POWER TO AN INTRAOCULAR IMPLANT - Many modem implantable ophthalmic devices include electronic components, such as electro-active cells, that can leak harmful substances into the eye and/or surrounding tissue. In the implantable ophthalmic devices disclosed herein, electronic components are hermetically sealed to facilitate mechanically connecting components of an implantable ophthalmic device. Furthermore, the device includes at least one battery with a surface comprising electrical contact portions, a housing for the at least one battery, a first wafer bonded to the housing such that the housing and the first wafer form a hermetically sealed surface around the battery, and an electronic circuit electrically connected to the electrical contact portions of the battery. | 2013-09-19 |
20130245756 | COPOLYMERS FOR INTRAOCULAR LENS SYSTEMS - Some embodiments provide a copolymer comprising: an acrylate recurring unit and an optionally substituted vinylaryl recurring unit, wherein a portion of at least one of the recurring units comprises a vinyldialkylsiloxy pendant group. The copolymers may be useful as soft acrylic haptics for intraocular lenses. Some embodiments further relate to intraocular lenses having a hydrophobic soft acrylic optic and a silicone haptic, such as a dual optic accommodative lens a having hydrophobic soft acrylic anterior and posterior optic bodies and a silicone haptic. Related copolymeric composite materials as well as additional embodiments of intraocular lenses, are also described herein. | 2013-09-19 |
20130245757 | METHOD AND DEVICE FOR IMPROVED SOFT TISSUE SURGERY - Methods for determining suitability of an implantable silk scaffold for use in human soft tissue repair by implanting a silk scaffold in a quadruped. The silk scaffold is completely or essentially completely bioresorbed by twelve months after implantation, the silk scaffold (to the extent remaining) with ingrown tissue shows at least about a 60% strength increase by 12 months after implantation, and the thickness of the silk scaffold (to the extent remaining) with ingrown tissue increases by more than 100% by 12 months after implantation. | 2013-09-19 |
20130245758 | INFLATABLE PROSTHESES AND METHODS OF MAKING SAME - An inflatable tissue expander or more permanent prosthesis, suitable for implantation in a breast, is provided. | 2013-09-19 |
20130245759 | MEDICAL DEVICES INCORPORATING SILICONE NANOPARTICLES, AND USES THEREOF - Provided herein are uses of silicone nanoparticles as breast implant materials that reduce immunogenic responses, compared to other breast implant materials. | 2013-09-19 |
20130245760 | MEDICAL DEVICES INCORPORATING CERAGENIN-CONTAINING COMPOSITES - A medical device that includes a coating of a composite material that includes a polymeric material having a void structure and particulate ceragenin material (i.e., ceragenin particles) associated with the void structure. The average particle size of the ceragenin particles in the composite is in a range from 5 nm to 20 μm, 50 nm to 10 μm, 100 nm to 5 Ξm, or 1 μm to 10 μm. The composite has a high loading of ceragenin particles (e.g., about 10% to about 25%, by weight). The composite has good polymer stability, the ability to release ceragenins from the ceragenin particles disposed in the composite over a sustained period of time at a characteristic elution rate, and the ability to kill large numbers of bacteria and other susceptible microbes over the sustained period of time. | 2013-09-19 |
20130245761 | Method And Apparatus For Tibial Fixation Of An ACL Graft - A tensioner system for use in tensioning graft strands in a knee reconstruction procedure can include a handle assembly, a tensioner assembly coupled relative to the handle assembly, and a drive shaft slidably received through and supported by the handle assembly. The tensioner assembly can include an arm support member rotatably coupled to the handle assembly and first and second arm members each rotatably coupled to lateral sides of the arm support member. Each arm member can include at least one graft attachment area adapted to be coupled to a graft strand. The arm support member can be configured to rotate about an axis perpendicular to a longitudinal axis of the tensioner system and perpendicular to an axis of rotation of each of the arm members. The drive shaft can include proximal and distal ends that extend beyond respective proximal and distal ends of the handle assembly. | 2013-09-19 |
20130245762 | TENDON REPAIR IMPLANT AND METHOD OF ARTHROSCOPIC IMPLANTATION - A tendon repair implant for treatment of a partial thickness tear in the supraspinatus tendon of the shoulder is provided. The implant may incorporate features of rapid deployment and fixation by arthroscopic means that compliment current procedures; tensile properties that result in desired sharing of anatomical load between the implant and native tendon during rehabilitation; selected porosity and longitudinal pathways for tissue in-growth; sufficient cyclic straining of the implant in the longitudinal direction to promote remodeling of new tissue to tendon-like tissue; and, may include a bioresorbable construction to provide transfer of additional load to new tendon-like tissue and native tendon over time. | 2013-09-19 |
20130245763 | THREADED IMPLANT - A threaded implant includes a body, exterior surface, interior surface, fenestrations, and threads. The body may be a hollow tubular structure. Alternatively, the body may be solid and cannulated. The surface of the threaded implant may have mesh configuration, beaded configuration, trabecular configuration, holes or any surface conducive to bony in-growth, on-growth and/or through-growth. The threads may be barbed and may allow for easy insertion through the bone. The threaded implant may be tapped into place. A method for fusing bone may involve inserting the implant laterally through the ilium, through the sacral-iliac joint, and into the sacrum. | 2013-09-19 |
20130245764 | ARTIFICIAL SI JOINT - An artificial SI-Joint includes a sacrum component and an ilium component. The sacrum component may include a ridge, foundation, perimeter surface and a fitting member. The ilium component may include a polybearing, edge, foundation, perimeter surface, and a ridge or sockets. The fitting member of the sacrum component may engage the polybearing of the ilium component to restore normal movement of the SI-Joint. The artificial SI-Joint may be implanted as a single unit or as separate pieces that are coupled together. | 2013-09-19 |
20130245765 | TRANSCORPOREAL SPINAL DECOMPRESSION AND REPAIR SYSTEMS AND RELATED METHODS - A system and method are provided for making an access channel through a vertebral body to access a site of neural compression, decompressing it, and repairing the channel to restore vertebral integrity. System elements include an implantable vertebral plate, a guidance device for orienting bone cutting tools and controlling the path of a cutting tool, a bone cutting tool to make a channel in the vertebral body, a tool for opening or partially-resecting the posterior longitudinal ligament of the spine, a tool for retrieving a herniated disc, an implantable device with osteogenic material to fill the access channel, and a retention device that lockably-engages the bone plate to retain it in position after insertion. System elements may be included in a surgery to decompress an individual nerve root, the spinal cord, or the cauda equina when compressed, for example, by any of a herniated disc, an osteophyte, a thickened ligament arising from degenerative changes within the spine, a hematoma, or a tumor. | 2013-09-19 |
20130245766 | Artificial Disc - A medical device includes a base ring configured to be implanted within a body of a patient. The base ring provides a contact surface to a vertebrae. Multiple layers of multiple leveling plates are configured to equalize forces applied to the contact surface of the base ring, where at least one of the layers of the leveling plates engages an inner surface of the base ring. A layer of multiple pads is included with a top surface of the pads configured to maintain a parallel plane and a bottom surface of each of the multiple pads is configured to engage a top surface of one of the layers of the leveling plates. A cover is configured to enclose the multiple layers of the leveling plates, the layer of the multiple pads and the base ring. The cover provides a contact surface to a vertebrae. | 2013-09-19 |
20130245767 | INTERBODY VERTEBRAL PROSTHETIC AND ORTHOPEDIC FUSION DEVICE WITH SELF-DEPLOYING ANCHORS - A prosthesis includes: a body including a first major surface for engaging an endplate of a first vertebral bone of a spine, a second major surface for engaging an endplate of an adjacent, second vertebral bone of the spine; at least one aperture extending from within the body and opening at the first major surface; at least one anchoring element disposed within the aperture and including a shaft having proximal and distal ends; and a drive mechanism engaging the proximal end of the at least one anchoring element and operating to push the at least one anchoring element out through the at least one aperture and into the first vertebral bone, without rotating the at least one anchoring element about an axis thereof. | 2013-09-19 |
20130245768 | Apparatus and Methods for Inserting an Implant - A system and method for inserting an implant into a cavity is disclosed, which may include advancing an implant insertion instrument toward a pair of adjacent bodies, the implant insertion instrument having two opposed ramps, wherein each ramp has a distal tip and wherein the longitudinal axes of the opposed ramps are separated by an initial angle; inserting the distal tips of the opposed ramps between the adjacent bodies, thereby creating an initial interbody cavity between the adjacent bodies; expanding the interbody cavity while maintaining the initial angle between the longitudinal axes of the opposed ramps; placing the implant in a final location between the adjacent bodies; transferring a compressive force urging the adjacent bodies together from the opposed ramps to the implant; and extracting the implant insertion instrument from the interbody cavity. | 2013-09-19 |
20130245769 | INTERBODY DEVICE INSERTION SYSTEMS AND METHODS - Provided is a system for implanting an interbody device into a disc space located between a first and second vertebra includes a guide frame including a guide member having an opening. The system further includes an implant trial including an elongated body and a base plate coupled to the elongated body. The elongated body of the implant trial is releasably coupled to the guide member of the guide frame during use such that the opening guides longitudinal movement of the implant trial relative to the guide frame. The system still further includes a dilator operatively coupled to the elongated body during use for distracting the disc space. The system still further includes an insertion instrument including an elongated body and an insertion member coupled to the elongated body. The elongated body of the insertion instrument is releasably coupled to the guide member of the guide frame during use such that the opening guides longitudinal movement of the insertion instrument relative to the guide frame. The insertion member is releasably coupled to at least a portion of the interbody device during use. | 2013-09-19 |
20130245770 | MODULAR SEGMENTED DISC NUCLEUS IMPLANT - A segmented disc nucleus replacement prosthesis and system for its implantation wherein the segments are made of a compliant, homogeneous material throughout. The prosthesis comprises a plurality of modular segments that mate together in a rail-and-slot arrangement. The rails and slots are configured to interlock and hold together under load despite being formed of compliant materials. In one embodiment, insertion tools and stabilizers are utilized for manipulation of the modular segments, the insertion tools and stabilizers being designed to accommodate for handling the compliant modular segments. | 2013-09-19 |
20130245771 | METHOD FOR LOADING A SPINAL IMPLANT - A method for loading a spinal implant with fusion promoting substances into an implantation space adjacent vertebral bodies of the spine. | 2013-09-19 |
20130245772 | SOLID STATE DEFORMATION PROCESSING OF CROSSLINKED HIGH MOLECULAR WEIGHT POLYMERIC MATERIALS - Solid-state deformation processing of crosslinked high molecular weight polymers such as UHMWPE, for example by extrusion below the melt transition, produces materials with a combination of high tensile strength and high oxidative stability. The materials are especially suitable for use as bearing components in artificial hip and other implants. Treated bulk materials are anisotropic, with enhanced strength oriented along the axial direction. The material is oxidatively stable even after four weeks of accelerated aging in a pressure vessel containing five atmospheres of oxygen (ASTM F2003). Because of its oxidative stability, the deformation processed material is a suitable candidate for air-permeable packaging and gas sterilization, which has thus far been reserved for remelted crosslinked UHMWPE. | 2013-09-19 |
20130245773 | HIGHLY CRYSTALLINE CROSS-LINKED OXIDATION-RESISTANT POLYETHYLENE - The present invention relates to methods for making highly crystalline cross-linked polymeric material, for example, highly crystalline cross-linked ultra-high molecular weight polyethylene (UHMWPE). The invention also provides methods of making antioxidant-doped highly crystalline cross-linked polymeric material using high pressure and high temperature crystallization processes, medical implants made thereof, and materials used therein. | 2013-09-19 |
20130245774 | METHODS AND APPARATUS FOR DELIVERING AND POSITIONING SHEET-LIKE MATERIALS IN SURGERY - An implant delivery system for delivering a sheet-like implant is disclosed. The implant delivery system includes a distal guidewire port for receiving the proximal end of guidewire after the guidewire distal end has been affixed to a first point on bone or other tissue. The implant delivery system is tracked over the guidewire to a selected position defined by the guidewire attachment. The device includes an implant spreader assembly disposed proximate the distal end of a delivery shaft. The implant spreader assembly includes a first arm and a second arm. The arms are coupled to the delivery shaft such that the first arm and second arm are moveable between a closed position and an open position. When pivoting to the open position the distal end of each arm travels in a generally transverse direction to spread a sheet-like implant. | 2013-09-19 |
20130245775 | JOINT IMPLANT TRIAL COMPONENTS - A humeral component of a prosthesis comprises a stem module for fixing the prosthesis into a bone. A joint adapter can be attached, preferably under different angles to the stem module. The joint adapter holds a liner having a recessed spherical cavity, which is the cup of the joint. The joint adapter has an inner surface and a circumferential groove. The liner has an outer surface including a circular recess. This circular recess preferably is concentric to the major body diameter of the liner for interfacing with the circumferential groove of the joint adapter. Furthermore, the liner has a radial slit, which allows compression of the liner for easy insertion and removal. This allows inserting different liners with different sizes thus allowing to try out different sizes to find the best size for the patient. When the best size has been identified, a final liner without a slit may be inserted. | 2013-09-19 |
20130245776 | BONE PREPARATION TOOL KIT AND ASSOCIATED METHOD - A prosthesis ( | 2013-09-19 |
20130245777 | KNEE SYSTEM - A knee system includes a knee prosthesis having a tibial arrangement including a tibial tray configured for attachment to a surgically-prepared surface of a proximal end of the tibia. The tibial arrangement also includes a tibial insert system including a lateral tibial insert and a medial tibial insert. One of the inserts is configured to move in a generally anterior-posterior direction relative to the tibial tray, and the other insert is configured for fixed attachment to the tibial tray. The knee prosthesis also includes a femoral component configured for attachment to a surgically-prepared surface of a distal end of a femur. The femoral component and tibial inserts each have articular surfaces configured to contact and articulate relative to each other during extension and flexion of the knee. | 2013-09-19 |
20130245778 | PROSTHESIS FOR DISTAL RADIOULNAR JOINT - Among other things, there are disclosed embodiments of implants for repairing or relieving damage to the distal radioulnar joint. A component for replacing at least part of the ulnar head includes a concave surface for accommodating a convex surface of a component for attachment to the radius, e.g. in the sigmoid notch of the radius. | 2013-09-19 |
20130245779 | NECK SPARING TOTAL HIP IMPLANT METHODS - A femoral prosthesis. The femoral prosthesis includes an implant body having a proximal end and a distal end and a shoulder at the proximal end, the shoulder being structured and dimensioned for a tight press fit into the neck of a femur. The implant body includes a trunk at the distal end, the trunk having a wedge formed by a tapered portion extending in the direction of the distal end of the implant body. The implant body also includes a medial column extending from the shoulder toward the distal end and a lateral column extending from the shoulder toward the distal end. The wedge, the medial column, and the lateral column to provide multi-planar stability for the implant body and surface area for fixation of the implant body. | 2013-09-19 |
20130245780 | Acetabular Cartilage Implant - Disclosed is a system for replacing a portion of cartilage in an acetabulum. A prosthesis can be positioned within an acetabulum to form a portion of the articulation surface within the acetabulum and to articulate with a femoral bone. For example, an acetabular prosthesis can be implanted to articulate with the natural femoral head. | 2013-09-19 |
20130245781 | ACETABULAR CUP ASSEMBLY FOR MULTIPLE BEARING MATERIALS - A modular acetabular cup assembly ( | 2013-09-19 |
20130245782 | Modular Joint Prosthesis System, Premounted Joint Prosthesis System Part and Sterile Article - A modular hip joint prosthesis system has an intermediate element which has an inner cone for receiving a prosthesis neck and an outer cone, a joint hall head which is embodied as a plug head having an inner cone associated with the outer cone of the intermediate element, and a bipolar joint socket in which an inlay is received in the outer shell in a freely moving manner and which has a ball receiver which is associated with the joint ball head, configured, such that said joint ball head can be received in a movable manner. A premounted joint prosthesis system part for a modular joint prosthesis system and a sterile article are also provided. | 2013-09-19 |
20130245783 | Implant With Antimicrobial Coating - The invention relates to an implant with a coating ( | 2013-09-19 |
20130245784 | METHOD FOR FORMING A TISSUE CONSTRUCT AND USE THEREOF - The present invention relates to a method for forming a tissue construct having a composite structure. The method includes providing a biodegradable substrate, wherein the substrate is adapted to allow deposition or growth of a plurality of cells; providing a vascularized layer comprising a plurality of blood vessels therein; and adhering the vascularized layer to the substrate. | 2013-09-19 |
20130245785 | INTELLIGENT PROSTHETIC SOCKET SYSTEM WITH ACTIVE USER FEEDBACK INTERFACE AND REAL TIME PROSTHESIS DIAGNOSTICS - An apparatus is provided for use with a prosthetic system. The apparatus includes a housing that is disposed within a prosthetic socket. The housing has a vacuum pump and a switch. The a vacuum pump is actuated to maintain a negative air pressure within the prosthetic socket. The switch is configured to allow a user to operate the vacuum pump. | 2013-09-19 |
20130245786 | Pocketed Double Fabric Prosthetic Liner - A prosthetic liner having a base elastic fabric layer impregnated with cushioning material on an interior surface of the base fabric layer and having one or more additional elastic fabric layers secured to and overlapping the base fabric layer to form pockets for introducing and retaining various types of padding selected by the user. | 2013-09-19 |
20130245787 | Real-Time Flexible Vehicle Control Apparatus and Method - An apparatus on an integrated circuit, and method thereof, provides a real-time flexible interface between inputs from a vehicle components and outputs to the vehicle control components. The functions comprises of a programmable interconnection matrix, engine sensors and a control interface. Both engine sensors and control functions comprise of fixed hardwired functions and a customization hardware area. The apparatus therefore provides means for flexible powertrain events control target for the next generation of low-polluting power trains of vehicles. | 2013-09-19 |
20130245788 | NUMERICAL CONTROL SYSTEM USING I/O UNIT FOR TIME MEASUREMENT - In a numerical control system in which a numerical controller and an I/O unit perform serial data communication through a communication line, a counter of the I/O unit starts time measurement with an input signal from an in-machine measurement device as a trigger and stops counting at the start of transmission of DI data. The I/O unit transmits a flag indicative of input of the input signal as a trigger and a value in the stopped counter to the numerical controller. Based on a time value measured by a timer and the counter value, the numerical controller calculates the time of input of the input signal. | 2013-09-19 |
20130245789 | ELECTRIC TOOL AND DATA TRANSMISSION METHOD - An electric tool includes a motor, a light having a function in addition to a data transmission, a switch configured to switch power supply to the light in accordance with a user operation; and a control unit. Upon a switch is switched from OFF to ON, the light is blinked at a frequency above the human-sensible range on the basis of data such as the usage history data of the electric tool. An average of the blinking frequency of the light is approximately 4,800 Hz when a bit rate is set to 9,600 bps, for example. Further, an average of a duty ratio of a drive signal of the light during blinking is approximately 50%. | 2013-09-19 |
20130245790 | INFORMATION PROCESSING APPARATUS, INFORMATION PROCESSING METHOD, AND MEDIUM - An information processing apparatus controls position measurement performed by a position measurement device. The apparatus includes a memory and a processor that executes a process in the memory. The process includes acquiring schedule information associated with the position measurement device and including a start time and an end time, acquiring position information acquired by the position measurement device, and extending a position measurement cycle of the position measurement device compared to a position measurement cycle before the start time of the schedule information when positions that respectively correspond to a plurality of pieces of position information acquired between the start time and the end time are in a given area. | 2013-09-19 |
20130245791 | SYSTEM AND METHOD FOR PROTECTION SYSTEM DESIGN SUPPORT - A method and system for examining, auditing, and safely evaluating process systems, including fluid pressure systems and nuclear plant systems, to aid overpressure design and/or sizing of overpressure equipment. The system includes a server subsystem, a storage subsystem, an assessment subsystem, and optionally a report generation subsystem, including computer hardware and application software for supporting these subsystems. | 2013-09-19 |
20130245792 | CONTROL PROGRAM ADMINISTRATION SYSTEM AND METHOD FOR CHANGING CONTROL PROGRAM - A control arithmetic device controls so that an approval-receiving device displays a content of a new control program that the control arithmetic device received from the editing device. The approval-receiving device receives input of approval information that indicates whether a change of a control program is approved or not from an manager. The control arithmetic device changes the control program to the new control program in the case where the approval information received from the approval-receiving device indicates approval of the control program. | 2013-09-19 |