| 10th week of 2015 patent applcation highlights part 71 |
| Patent application number | Title | Published |
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| 20150066056 | CLAMP DEVICE FOR MINIMALLY INVASIVE PROCEDURES AND USES THEREOF - Provided herein is a clamp device that can be used in minimally invasive procedures, including surgeries such as laparoscopic surgeries, for clamping a tissue or an organ or a portion of a tissue or organ. Also provided herein are methods of clamping a tissue or an organ or a portion thereof during minimally invasive surgery using the clamp device provided herein. Also provided are systems for performing a minimally invasive surgery that include the clamp device for minimally invasive surgery provided herein and an injection device configured to access an endoscopic port for the minimally invasive surgery. | 2015-03-05 |
| 20150066057 | Surgical Clip Applier - A surgical clip applier is provided including a clip pusher bar having a flexible tab and a camming plate configured to effectuate closure of the pair of jaws. The camming plate includes a lost motion portion and the flexible tab is configured to engage the lost motion portion during an initial movement of the clip pusher bar to cause the camming plate to move with the clip pusher bar. The flexible tab is configured to disengage from the lost motion portion during a subsequent movement of the clip pusher bar to allow the clip pusher bar to move relative to the camming plate. | 2015-03-05 |
| 20150066058 | METHOD AND APPARATUS FOR MENISCAL REPAIR - A cleat for securing suture to tissue, the cleat comprising an elongated body having a distal end and a proximal end, the distal end having a distal slot extending proximally into the elongated body, and the proximal end having a proximal slot extending distally into the body; the distal slot comprising a wide section and a narrow section, wherein the wide section has a width such that the suture is slidably accommodated therein and the narrow section has a width such that the suture is bound therein, and further wherein the wide section is disposed distally of the narrow section. A method for securing a first object to a second object, the method comprising providing a suture and a plurality of cleats slidably mounted on the suture; passing one end of the suture and a first cleat through the first object and the second object; tensioning the suture so as to secure the suture to the first cleat; passing a subsequent portion of the suture and a second cleat through the first object and the second object; and tensioning the suture so as to secure the suture to the second cleat. | 2015-03-05 |
| 20150066059 | SOFT TISSUE REPAIR - Methods and instruments for repairing soft tissues of a skeletal joint such as for example of the foot or hand are presented. | 2015-03-05 |
| 20150066060 | Methods for Tissue Repair - A method of closing a tissue wound includes providing a wound closure device having a first fastener, a second fastener, and a flexible member extending between the first and second fasteners and movably attached to the second fastener by a one-way knot formed in the flexible member between the first and second fastener, positioning the first fastener against tissue, passing the flexible member across the wound, positioning the second fastener against tissue, and pulling on a free end of the flexible member to shorten a length of the flexible member between the first and second fasteners, thereby closing the wound. | 2015-03-05 |
| 20150066061 | METHOD AND APPARATUS FOR MENISCAL REPAIR - An anchor for securing suture to tissue, the anchor comprising:
| 2015-03-05 |
| 20150066062 | SURGICAL INSTRUMENT FOR DEPLOYING A PROSTHESIS - The present invention relates to a surgical instrument ( | 2015-03-05 |
| 20150066063 | Surgical Implant - A surgical implant ( | 2015-03-05 |
| 20150066064 | TISSUE STABILIZATION SYSTEM - Methods and systems are provided for tissue stabilization. Some aspects include a carrier member having a length, width, and thickness, wherein the length and width are each at least two times greater than the thickness; attachment members extending from the carrier member and that engage connective tissue; and stabilizing members, each of which can couple a respective attachment member to the carrier member and is substantially positionally fixed relative to the carrier member. | 2015-03-05 |
| 20150066065 | INSERTABLE PROSTHESIS AND PROSTHESIS BOARD FOR ANASTOMOSIS - Prosthetic devices are provided used for anastomosis of extremity with lateral, extremity with extremity and lateral with lateral without clamping and sutureless or with quick clamping sutureless, in which the graft is inserted in at least one of the intraluminal parts of the tubular member of the insertable prosthesis, the flanges including lateral inserts allowing the configuration of different prosthesis sets. Also described is a board of prostheses including one flange with multiple holes through which intraluminal parts or occluders will be inserted, according to the need of the anastomosis to be carried out. Also provided are prostheses in which the grafts cover only externally their extraluminal parts. | 2015-03-05 |
| 20150066066 | ADJUSTABLE VASCULAR RING, MEANS FOR TREATING SFS SYNDROME AND IMPLANTABLE KIT COMPRISING SUCH A RING, MOULD AND METHOD FOR OBTAINING SUCH A RING - The invention relates to a perivascular ring having an inner diameter adjustable by inflation/deflation and adapted to be implanted and closed about a vessel for controlling the inner diameter of said vessel and thus the flow and/or pressure of a fluid flowing in said vessel. The ring of the invention is capable of regulating blood flow to the liver, in particular after an hepatectomy or hepatic transplant, and to substantially improve the survival chances of the patient. The ring according the invention has an adjustable inner diameter (φ | 2015-03-05 |
| 20150066067 | ULTRASONIC SURGICAL INSTRUMENTS - An ultrasonic surgical blade comprising a body having a proximal end and a distal end. The distal end of the body is movable relative to a longitudinal axis by vibrations produced by a transducer. The body comprises a longitudinally extending bore formed within the ultrasonic surgical blade. The ultrasonic surgical blade is configured to emit a spray from the bore at the distal end thereof to substantially prevent fluid from contacting the distal end of the ultrasonic surgical blade. | 2015-03-05 |
| 20150066068 | BALLOON CATHETER - A balloon catheter includes an outer conduit having an outer surface, and an inner conduit having an outer surface. The inner conduit is suitable for passage over a guide wire, and the inner conduit is movably disposed within the lumen of the outer conduit. There is also a balloon having a proximal margin and a distal margin, such that the proximal margin of the balloon is attached to the outer surface of the distal tip of the outer conduit and the distal margin of the balloon is attached to the outer surface of the portion of the inner conduit that extends beyond the distal tip of the outer conduit. And there is a fluid port for introducing an expansion fluid into the annular space formed between the inner surface of the outer conduit and the outer surface of the inner conduit and into the lumen of the balloon, and for the removal of the expansion fluid. | 2015-03-05 |
| 20150066069 | Valvuloplasty Catheter And Methods - A valvuloplasty catheter has a dog-bone shaped balloon with semi-compliant smaller diameter waist and non-compliant larger diameter bulbous end regions. The balloon centers across the valve with the waist adjacent to the annulus. One bulbous region serves to hyperextend the valve leaflets and the other assists in stabilizing the balloon position to reduce migration. The semi-compliant waist increases in diameter as fluid enters the balloon until it comes into contact with the valve annulus. The pressure within the balloon per unit of volume delivery has a greater slope after contact with the annulus than before resulting in a change in slope for the pressure versus volume curve. The diameter of the balloon and annulus are determined at this inflection point when the balloon contacts the annulus. | 2015-03-05 |
| 20150066070 | SIDE BRANCH BALLOON - An improved balloon catheter structure includes a beveled distal tip, a reinforced distal portion, and an elastic or split sleeve over at least a portion of the balloon. The balloon may have a short length and a marker at its midline. The catheters are particularly useful for crossing through stent walls at vessel bifurcations. | 2015-03-05 |
| 20150066071 | NASAL DILATOR AND BOUGIE - A nasal dilator and bougie is disclosed. The dilator includes, for example, an elongated member terminating in an end and a slidable member having a terminal end movable to the end of the elongated member in a first position. A dilation portion at the end of the elongated member has a first diameter and a second diameter greater than the first diameter when the slidable member is in the first position. An actuator can move the slidable member. | 2015-03-05 |
| 20150066072 | CATHETER LUMEN PARTITIONER - A catheter lumen partitioner and methods for treating aneurysm are disclosed. | 2015-03-05 |
| 20150066073 | DETACHMENT MECHANISMS FOR IMPLANTABLE DEVICES - The present invention relates to detachment mechanisms for delivering and releasing implantable devices into a body lumen. According to certain aspects, systems of the invention include a junction that couples an implantable device to a delivery member. The junction includes an anodic portion and a cathodic portion galvanically coupled to the anodic portion such that the anodic portion corrodes when exposed to an electrolytic fluid, thereby detaching the implantable device from the delivery member without application of energy from an external power source. | 2015-03-05 |
| 20150066074 | MEDICAL DEVICE FOR MODIFICATION OF LEFT ATRIAL APPENDAGE AND RELATED SYSTEMS AND METHODS - Several embodiments are set forth of devices, systems and methods for modifying an atrial appendage such as a left atrial appendage (LAA). In one embodiment, a medical device includes a frame member and a tissue growth member. The frame member includes a unitary, seamless central portion having a plurality of struts defining a multi-cellular structure and an anchoring system, the plurality of struts extending between and configured to self-expand and directly bias the anchor system to anchor the frame member at least partially within the LAA. With this arrangement, the tissue growth member is attached to the frame member to occlude the LAA. | 2015-03-05 |
| 20150066075 | INTRODUCER SHEATH WITH EMBOLIC PROTECTION - The embolic protection device comprises an embolic filter attached to an inner sheath. The embolic filter includes at least a first catheter access port and a second catheter port. At least the first catheter port will typically be radially expandable to receive catheters of different diameters and will be located at an atypical end of an aero conical structure at a downstream end of the filter. | 2015-03-05 |
| 20150066076 | SURGICAL FORCEPS - A forceps includes an end effector assembly having first and second jaw members movable between a spaced-apart position and an approximated position for grasping tissue therebetween. A knife assembly having a cutting blade disposed at a distal end thereof is also provided. The knife assembly is translatable relative to the end effector assembly between a retracted position and an extended position, wherein the cutting blade extends between the jaw members to cut tissue grasped therebetween. The knife assembly includes a proximal component and a first distal component that includes the cutting blade. The proximal and first distal components are removably coupled to one another to facilitate replacement of the first distal component while the end effector assembly remains in a substantially assembled condition, i.e., without requiring substantial disassembly of the end effector assembly. | 2015-03-05 |
| 20150066077 | Device For Occluding An Opening In A Body And Associated Methods - The disclosure relates to a device for occluding an opening in a body and associated methods. The device of this disclosure has the advantage that a second element of the device can be made more flexible than a first element and thereby the device is less prone to increase the rupture size of an opening. In one example, a device ( | 2015-03-05 |
| 20150066078 | Looped Tissue Fixation Device - A tissue fixation device includes a barbed body in a general figure eight configuration including a first loop intersecting a second loop. The barbed body may include a third loop at a proximal end thereof, and/or a pledget at a distal end thereof. The configuration of the tissue fixation device may vary depending upon the performance requirements desired of the tissue fixation device for the envisaged application of use. | 2015-03-05 |
| 20150066079 | SUTURE TAPE WITH EXTERIOR SUTURE STRANDS - Tape constructs for fixation of soft tissue to bone, or of soft tissue to soft tissue. The tape construct includes a thin tape material with at least one thread positioned on the exterior of the thin tape material. Preferably, two threads are provided only on the exterior of the thin tape material, the threads extending in a direction about longitudinal with the thin tape material and abutting the edges or rims of the tape. The two exterior threads act like a parachute for compression of tissue and also allow the tape to fold easily to reduce the diameter of the tape construct for tissue passing and instrument passing. The construct is a simple, collapsible, flexible, parachute-like structure that allows easy threading and passing through instruments. | 2015-03-05 |
| 20150066080 | High-Strength Multi-Component Suture - A method for making an expanded, and optionally multi-component and/or colored PTFE monofilament is disclosed. The method includes forming a first paste by mixing a PTFE powder with a hydrocarbon solvent; forming an extrusion preform by pressing the first paste into a form; curing the extrusion preform by exposing the extrusion preform to a first temperature for a first time duration; forming a green monofilament by extruding the first paste through a die; expanding the green monofilament by exposing the green monofilament to a second temperature for a second time duration, the second time duration occurring after the first time duration; stretching the green monofilament substantially along a longitudinal axis of the green monofilament, the stretching the green monofilament occurring after the expanding the green monofilament; and sintering the green monofilament after the stretching the green monofilament. The method may include doing all or some of the expanding, stretching and sintering steps simultaneously. | 2015-03-05 |
| 20150066081 | VARIABLE DENIER YARN AND SUTURE - A method of suturing includes: (1) wrapping a first segment of a suture through a traction loop; (2) pulling the traction loop and the first segment through an opening in a suture lock; (3) continuing to pull the traction loop such that a second segment of the suture extends through the opening, wherein the second segment has a greater denier than the first segment such that the second segment more nearly fills an entire dimension of the opening than the first segment; and (4) locking the suture in place with the second segment in the opening. | 2015-03-05 |
| 20150066082 | CARDIAC TISSUE ANCHORING DEVICES, METHODS, AND SYSTEMS FOR TREATMENT OF CONGESTIVE HEART FAILURE AND OTHER CONDITIONS - A heart tissue gripping device may include a body portion, an elongate shaft, and a tissue gripping member that is attached to the distal end of the elongate shaft. The tissue gripping member being may be positioned adjacent a heart surface by insertion through an incision in the body. The tissue gripping member may releasably attach to tissue of the heart surface to facilitate a surgical instrument in performing one or more procedures. A coupling of the tissue gripping member may releasably attach the surgical device to the tissue gripping member to allow the device to access the tissue of the heart surface. | 2015-03-05 |
| 20150066083 | PACIFIER WITH MANETIC COUNTERWEIGHT BASE - A pacifier with magnetic counterweight base; The invention is of a pacifier with nipple and a round body and also a magnetic counterweight base which counter acts the weight of the nipple and forces the nipple to stay upright on any surface the pacifier is placed. The magnetic base allows for mounting to any metal surface or specifically designed clothing. | 2015-03-05 |
| 20150066084 | Instrument Kit for Spinal Osteosynthesis - A surgical kit for fastening vertebrae via the posterior approach or via the posterolateral approach, comprising: at least one vertebral or pedicle screw, and a fitting tube co-operating with the screw; the fitting tube having two rigid branches, each of the two branches having, on the inside face of its proximal end, at least one shoulder; the kit further comprising a retractable securing insert for securing together the branches; wherein the screw head has at least two longitudinal extensions, extending in the distal direction, each of said extensions being configured to enable said screw head to be inserted into a space of complementary shape formed between the inside surface of the proximal end of one of the rigid branches and the outside surface of the proximal end of said retractable insert, when the retractable insert is fully engaged in the fitting tube. | 2015-03-05 |
| 20150066085 | Systems and Methods for Internal Bone Fixation - Internal bone fixation devices and methods for using the devices for repairing a weakened or fractured bone are disclosed herein. A device for use in repairing a fractured bone includes a delivery catheter having an elongated shaft with a proximal end, a distal end, and a longitudinal axis therebetween, wherein the delivery catheter has an inner void for passage of at least one reinforcing material and an inner lumen for passage of a light source; a conformable member releasably engaging the distal end of the delivery catheter, wherein the conformable member moves from a deflated state to an inflated state when the at least one reinforcing material is delivered to the conformable member; and an adapter releasably engaging the proximal end of the delivery catheter for receiving the light source and the at least one reinforcing material. | 2015-03-05 |
| 20150066086 | IMPLANT FOR STABILIZING SPINOUS PROCESSES - An implant for stabilizing spinous processes of adjacent vertebral bodies can include first and second contact elements. The first contact element is placed onto a first side of the spinous processes and the second contact element is placed onto a second side of the spinous processes. The implant includes at least one clamping element which couples to the first contact element, can be moved relative to the second contact element, and extends through the intervertebral space between the spinous processes and the second contact element. The implant also includes at least one fixing element on the second contact element which can be brought into engagement with the at least one clamping element to clamp the second contact element in the direction of the first contact element along the at least one clamping element. The first contact element is movable relative to the at least one clamping element. | 2015-03-05 |
| 20150066087 | Spinous Process Fusion Devices - The present disclosure generally relates to a device for positioning and immobilizing at least two adjacent vertebrae. In particular, in one or more embodiments, the present disclosure relates to spinous process fusion devices that distract and immobilize the spinous processes of adjacent vertebrae. | 2015-03-05 |
| 20150066088 | SURGICAL INSTRUMENT AND METHOD - A surgical instrument includes a first member defining a longitudinal axis. A second member is disposed with the first member and is axially translatable relative to the first member. A first body is connected to the first member and is translatable along an arcuate path relative to the first member. The first body is connected to a first implant support. A second body is connected to the second member and is translatable along an arcuate path relative to the second member. The second body is connected to a second implant support. Systems and methods of use are disclosed. | 2015-03-05 |
| 20150066089 | ROD PERSUADER, SYSTEM AND METHOD - A spinal rod persuader, system and method can include an outer tube, an inner tube, and a locking element. A first actuation mechanism can be movable in a linear fashion along a longitudinal axis direction to cause the locking element to move in a linear fashion over the inner tube and to lock the inner tube onto a pedicle screw. A second actuation mechanism can be rotated to cause the outer tube to move in a longitudinal axis direction with respect to the inner tube to push the spinal rod into a final position with respect to the pedicle screw while the pedicle screw is locked to the inner tube. A slot and/or tab structure can be provided in the outer tube such that actuation of the slot/tab will allow disassembly of the inner tube, outer tube and locking element with respect to each other. | 2015-03-05 |
| 20150066090 | SPINAL IMPLANT - This disclosure relates to a spinal implant that can provisionally retain a rod in an assembly head without having to first lock the rod relative to the assembly head. The spinal implant has a clip insert structured to retain the rod in the assembly head. The clip insert has a top portion with a cylindrical opening and extending over the cylindrical opening to cover the connection rod in part when the connection rod is engaged in the clip insert. The top portion is deformable by application of force on the connection rod to engage the connection rod with the clip insert. The clip insert and the assembly head are mechanically decoupled and can be fully received within the assembly head. The mechanical forces to which the assembly head is subjected are not transmitted to the clip insert. | 2015-03-05 |
| 20150066091 | SYSTEMS FOR VERTEBRAL ADJUSTMENTS AND ROD REDUCTION - An instrument for compression and distraction of a vertebral segment and reducing a surgical rod includes a first arm, a second arm, a coupler, and a reducer. The first arm includes a first aperture for receiving a first screw extender that attaches to a first vertebra. The second arm pivotably couples to the first arm and includes a second aperture for receiving a second screw extender that attaches to a second vertebra. The coupler links the first arm to the second arm to position the first arm relative to the second arm for compression and distraction of the first vertebra relative to the second vertebra. The reducer is received within the second aperture for reducing a surgical rod within the second screw extender. | 2015-03-05 |
| 20150066092 | SPINE STABILIZATION SYSTEM WITH SELF-CUTTING ROD - A spine stabilization system is provided. The system utilizes a self-cutting rod having a sharp cutting edge that can be anchored to a patient's spine with pedicle screws. The system can be percutaneously delivered, low profile, and allow cutting of surrounding tissue rather than simply spreading the tissue apart during rod insertion. | 2015-03-05 |
| 20150066093 | PROXIMAL TIBIAL POSTERIOR PLATEAU LOCKING COMPRESSION PLATE - A proximal posterior tibial plateau locking compression plate is revealed. This locking compression plate mainly includes a fixing plate and a pressing head having at least one threaded fixing hole and bent forward from the fixing plate. At least one lateral threaded fixing hole is arranged along the two sides the fixing plate and a plurality of lower threaded fixing holes is disposed on the fixing plate, extending downward. The threaded fixing hole on the pressing head, each lateral threaded fixing hole and each lower threaded fixing hole are mounted with a threaded fastener. Thereby the fractured bone fragments on the rear side of the proximal tibia, including those avulsed by the posterior cruciate ligament, are reduced anatomically and fixated rigidly. This locking compression plate not only allows the surgical staff to treat the fractured bone conveniently but also enables the patient to regain their pre-injury activities smoothly. | 2015-03-05 |
| 20150066094 | ORTHOPEDIC IMPLANT IN THE FORM OF A PLATE TO BE FIXED BETWEEN TWO BONE PARTS - A plate is disclosed for compressing together first and second bone parts. The plate includes screw holes adapted to receive screws for insertion into first and second bone parts, respectively, at least one of the screw holes being a compression slot with formations configured to ensure, when a respective screw is seated within the slot, an adjustable compression force adapted to bring the first and second bone parts closer together. The plate also comprises a circular guide pin hole for insertion of a pin into one of the first and second bone parts, and another guide pin hole, in the form of an elongate slot, for insertion of a pin into the other of the first and second bone parts. The plate may also include a curvature adapted to cause at least a pair of screws inserted into screw holes of the plate to converge. | 2015-03-05 |
| 20150066095 | SYSTEMS AND METHODS FOR USING POLYAXIAL PLATES - Certain embodiments of the invention provide plates for treating periarticular fractures or other non-full body weight bearing applications that combine polyaxial fixation with a low profile and enhanced contouring that more closely conforms to bone. Such plates can be designed to achieve buttressing effect and/or to be used in a reinforcement mode. Other features can be combined with these. Such plates can be created for use on bone sites such as on a tibia, fibula, metatarsal, calcaneous, other foot bone, humerus, radius, ulna, spinal, maxillofacial, as well as sites on other bones. | 2015-03-05 |
| 20150066096 | CERVICAL PLATE WITH A FEEDBACK DEVICE FOR SELECTIVE ASSOCIATION WITH BONE SCREW BLOCKING MECHANISM - A bone plate having at least one screw hole adapted to receive a bone screw, a blocker having a blocking end for blocking a bone screw from further backout of bone the blocker being predisposed in a blocking position wherein the blocking end at least partially overlaps a portion of the screw hole, the blocker being moveable from the blocking position by contact with the bone screw during insertion of the bone screw into the screw hole, and a blocker fixation element having an open orientation at which the blocker can move from the blocking position and a closed orientation preventing substantial movement of the blocker from the blocking position. The blocker fixation element cannot be moved to the closed orientation unless the screw head passes the blocker, thereby revealing that the blocker fixation element is in position to prevent substantial movement of the blocker. | 2015-03-05 |
| 20150066097 | BONE ANCHOR AND BONE ANCHOR ASSEMBLY COMPRISING THE SAME - A bone anchor ( | 2015-03-05 |
| 20150066098 | SYMMETRICAL OUTPUT NEUROSTIMULATION DEVICE - A method and system of providing therapy to a patient using electrodes implanted adjacent tissue. The method comprises regulating a first voltage at an anode of the electrodes relative to the tissue, regulating a second voltage at a cathode of the electrodes relative to the tissue, and conveying electrical stimulation energy between the anode at the first voltage and the cathode at the second voltage, thereby stimulating the neural tissue. The system comprises a grounding electrode configured for being placed in contact with the tissue, electrical terminals configured for being respectively coupled to the electrodes, a first regulator configured for being electrically coupled between an anode of the electrodes and the grounding electrode, a second regulator configured for being electrically coupled between an anode of the electrodes and the grounding electrode, and control circuitry configured for controlling the regulators to convey electrical stimulation energy between the anode and cathode. | 2015-03-05 |
| 20150066099 | METHODS, SYSTEMS, AND DEVICES FOR PAIRING VAGUS NERVE STIMULATION WITH MOTOR THERAPY IN STROKE PATIENTS - A method of treating motor deficits in a stroke patient, comprising assessing a patient's motor deficits, determining therapeutic goals for the patient, based on the patient's motor deficits, selecting therapeutic tasks based on the therapeutic goals, performing each of the selected therapeutic tasks repetitively, observing the performance of the therapeutic tasks, initiating the stimulation of the vagus nerve manually at approximately a predetermined moment during the performance of the therapeutic tasks, stimulating the vagus nerve of the patient during the performance of the selected therapeutic tasks, and improving the patient's motor deficits. | 2015-03-05 |
| 20150066100 | METHODS, SYSTEMS, AND DEVICES FOR PAIRING VAGUS NERVE STIMULATION WITH MOTOR THERAPY IN STROKE PATIENTS - A method of treating motor deficits in a stroke patient, comprising assessing a patient's motor deficits, determining therapeutic goals for the patient, based on the patient's motor deficits, selecting therapeutic tasks based on the therapeutic goals, performing each of the selected therapeutic tasks repetitively, observing the performance of the therapeutic tasks, initiating the stimulation of the vagus nerve manually at approximately a predetermined moment during the performance of the therapeutic tasks, stimulating the vagus nerve of the patient during the performance of the selected therapeutic tasks, and improving the patient's motor deficits. | 2015-03-05 |
| 20150066101 | METHODS, SYSTEMS, AND DEVICES FOR PAIRING VAGUS NERVE STIMULATION WITH MOTOR THERAPY IN STROKE PATIENTS - A method of treating motor deficits in a stroke patient, comprising assessing a patient's motor deficits, determining therapeutic goals for the patient, based on the patient's motor deficits, selecting therapeutic tasks based on the therapeutic goals, performing each of the selected therapeutic tasks repetitively, observing the performance of the therapeutic tasks, initiating the stimulation of the vagus nerve manually at approximately a predetermined moment during the performance of the therapeutic tasks, stimulating the vagus nerve of the patient during the performance of the selected therapeutic tasks, and improving the patient's motor deficits. | 2015-03-05 |
| 20150066102 | UNWANTED STIMULATION DETECTION DURING CARDIAC PACING - The disclosure relates to systems and methods for cardiac rhythm management. In some cases, a system may include a pulse generator for generating pacing pulses for stimulating a heart of a patient; a memory; and a sensor configured to sense a response to a unwanted stimulation and to produce a corresponding sensor signal. A processing circuit may receive the sensor signal for a time after one or more pacing pulses, and may derive a time-frequency representation of the sensor signal based on the received sensor signal. The processing circuit may use the time-frequency representation of the sensor signal to help identify unwanted stimulation. Once unwanted stimulation is detected, the processing circuit may change the pacing pulses to help reduce or eliminate the unwanted stimulation. | 2015-03-05 |
| 20150066103 | UNWANTED STIMULATION DETECTION DURING CARDIAC PACING - The disclosure relates to systems and methods for cardiac rhythm management. In some cases, a system may include a pulse generator for generating pacing pulses for stimulating a heart of a patient; a memory; and a sensor configured to sense a response to a unwanted stimulation and to produce a corresponding sensor signal. A processing circuit may receive the sensor signal for a time after one or more pacing pulses, and may derive a time-frequency representation of the sensor signal based on the received sensor signal. The processing circuit may use the time-frequency representation of the sensor signal to help identify unwanted stimulation. Once unwanted stimulation is detected, the processing circuit may change the pacing pulses to help reduce or eliminate the unwanted stimulation. | 2015-03-05 |
| 20150066104 | METHOD AND SYSTEM FOR PROVIDING ELECTRICAL STIMULATION TO A USER - A method for providing electrical stimulation to a user as a user performs a set of tasks during a time window, the method comprising: providing an electrical stimulation treatment, characterized by a stimulation parameter and a set of portions, to a brain region of the user in association with the time window; for each task of the set of tasks: receiving a signal stream characterizing a neurological state of the user; from the signal stream, identifying a neurological signature characterizing the neurological state associated with the task; and modulating the electrical stimulation treatment provided to the brain region of the user based upon the neurological signature, wherein modulating comprises delivering a portion of the set of portions of the electrical stimulation treatment to the brain region of the user, while maintaining an aggregate amount of the stimulation parameter of the treatment provided during the time window below a maximum limit. | 2015-03-05 |
| 20150066105 | SYSTEMS AND METHODS FOR TREATING ESSENTIAL TREMOR OR RESTLESS LEG SYNDROME USING SPINAL CORD STIMULATION - A method for treating essential tremor or restless leg syndrome using spinal cord stimulation includes implanting a lead near a spinal cord of a patient. The lead includes a plurality of electrodes disposed on a distal end of the lead and electrically coupled to at least one contact terminal disposed on a proximal end of the lead. Electrical signals are provided from a control module coupled to the lead to stimulate a portion of the spinal cord of the patient using at least one of the electrodes. The electrical signals reduce, alleviate, or eliminate at least one adverse effect of essential tremor or restless leg syndrome. | 2015-03-05 |
| 20150066106 | Flexible Circuit Electrode Array Embedded in a Cured Body - Polymer materials are useful as electrode array bodies for neural stimulation. They are particularly useful for retinal stimulation to create artificial vision, cochlear stimulation to create artificial hearing, and cortical stimulation, and many related purposes. The pressure applied against the retina, or other neural tissue, by an electrode array is critical. Too little pressure causes increased electrical resistance, along with electric field dispersion. Too much pressure may block blood flow. Common flexible circuit fabrication techniques generally require that a flexible circuit electrode array be made flat. Since neural tissue is almost never flat, a flat array will necessarily apply uneven pressure. Further, the edges of a flexible circuit polymer array may be sharp and cut the delicate neural tissue. It is advantageous that the array edges not contact tissue. | 2015-03-05 |
| 20150066107 | SYSTEM AND METHOD FOR ANIMAL-HUMAN NEURAL INTERFACE - Aspects of the invention include system and method for transmitting neural data extracted from an electrical signal of a non-human mammal to a human. The system includes an electrode implantable into the animal auditory nerve, brainstem, or midbrain of the non-human mammal, configured to record the electrical signal of the non-human mammal, the electrical signal being in the form of sequences of pulses or pulse trains encoding frequency information of the non-human mammal, a processing device electrically coupled with the electrode, configured to process the electrical signal and convert the processed electrical signal into a digital signal, a transmitting device electrically coupled with the processing device, configured to transmit the digital signal, and a receiving device electrically coupled with the transmitting device, configured to receive the transmitted digital signal, convert the received digital signal into a sensory output perceptible to the human, and apply the sensory output to the human. | 2015-03-05 |
| 20150066108 | SYSTEMS AND METHOD OF ADJUSTING THE COMPLIANCE VOLTAGE IN A NEUROMODULATION DEVICE - A therapeutic neuromodulation system configured for providing therapy to a patient. The therapeutic neuromodulation system comprises a plurality of electrical terminals configured for being respectively coupled to a plurality of electrodes implanted within tissue, analog output circuitry configured for delivering therapeutic electrical energy between the plurality of electrical terminals in accordance with a set of modulation parameters that includes a defined current value, a voltage regulator configured for supplying an adjustable compliance voltage to the analog output circuitry, and control/processing circuitry configured for automatically performing a compliance voltage calibration process at a compliance voltage adjustment interval by periodically computing an adjusted compliance voltage value as a function of a compliance voltage margin. The control/processing circuitry may also be configured for automatically adjusting at least one of the compliance voltage adjustment interval and the compliance voltage margin during the compliance voltage calibration process. | 2015-03-05 |
| 20150066109 | Methods and Systems of Electrode Polarity Switching in Electrical Stimulation Therapy - Methods for electrically stimulating body tissues to improve function or reduce symptoms provide an electrical stimulation system having two or more electrodes that are capable of being switched independently from a hyperpolarizing (depolarizing) state to a hypopolarizing state. Multiple combinations of hyperpolarizing electrodes and hypopolarizing electrodes are created by polarity switching to determine a polarity configuration having the best performance as determined by symptom reporting and clinical diagnostic tests. Polarity switching is triggered manually or is programmed to be switched automatically. Determining the configuration providing electrical stimulation resulting in the greatest benefit allows the system to be operated with one or more electrodes in a hypopolarizing state, thereby reducing energy requirements, tissue tolerance, and tissue fatigue. | 2015-03-05 |
| 20150066110 | Medical Device Application for an External Device Using Data Logged at an Implantable Medical Device - A Medical Device Application (MDA) is disclosed for an external device (e.g., a cell phone) that can communicate with an Implantable Medical Device (IMD). The MDA receives data logged in the IMD, processes that data in manners reviewable by an IMD patient, and that can control the IMD based on such processed data. The MDA can use the logged data to adjust IMD therapy based on patient activity or posture, and allows a patient to learn optimal therapy settings for particular activities. The MDA can also use the logged data to allow a patient to review details about IMD battery performance, whether such battery is primary or rechargeable, and to control stimulation parameters based on that performance. The MDA also allows a patient to enter medicine dose information, to review the relationship between medicinal therapy and IMD therapy, and to adjust IMD therapy based on the dosing information. | 2015-03-05 |
| 20150066111 | PROGRAMMING INTERFACE FOR SPINAL CORD NEUROMODULATION - A tool for assisting in the planning or performing of electrical neuromodulation of a patient's spinal cord. The tool may have various functions and capabilities, including calculating a volume of activation, registering an electrode(s) shown in a radiologic image, constructing functional images of the patient's spinal anatomy, targeting of neuromodulation, finding a functional midline between multiple electrodes, determining the three-dimensional position of multiple electrodes, and/or accommodating for electrode migration. In certain embodiments, the tool can be embodied as computer software or a computer system. | 2015-03-05 |
| 20150066112 | METHOD FOR CONTROLLING TELEMETRY IN AN IMPLANTABLE MEDICAL DEVICE BASED ON POWER SOURCE CAPACITY - An implantable microstimulator configured for implantation beneath a patient's skin for tissue stimulation to prevent and/or treat various disorders, uses a self-contained power source. Periodic or occasional replenishment of the power source is accomplished, for example, by inductive coupling with an external device. A bidirectional telemetry link allows the microstimulator to provide information regarding the system's status, including the power source's charge level, and stimulation parameter states. Processing circuitry automatically controls the applied stimulation pulses to match a set of programmed stimulation parameters established for a particular patient. The microstimulator preferably has a cylindrical hermetically sealed case having a length no greater than about 27 mm and a diameter no greater than about 3.3 mm. A reference electrode is located on one end of the case and an active electrode is located on the other end. The case is externally coated on selected areas with conductive and non-conductive materials. | 2015-03-05 |
| 20150066113 | Radiolucent Metal Case Plate to Facilitate Communications in an Implantable Medical Device - Disclosed is an improved case for an implantable medical device having an internal communication coil in which a lower-conductivity, more-radiolucent metallic plate is provided proximate to the coil. The remainder of the case can be formed of a higher-conductivity metallic material which is easier to form and thus lends itself to the manufacture of implantable medical devices with smaller cases for example. As both the plate and the remainder of the case are metallic, they can be easily joined by reliable laser welding techniques for example. | 2015-03-05 |
| 20150066114 | Construction for an Implantable Medical Device Employing an Internal Support Structure - Disclosed are designs and methods of construction for an implantable medical device employing an internal support structure. The single-piece support structure holds various electronic components such as a communication coil and a circuit board, and further is affixed to a battery, thus providing a subassembly that is mechanically robust. The support structure further provides electrical isolation between these and other components. Method of construction allows for the subassembly to be adhered to a case of the implantable medical device at the support structure, and possibly also at the battery, without electrically shorting the battery to the case. | 2015-03-05 |
| 20150066115 | Construction for an Implantable Medical Device Having a Battery Affixed to the Case - Disclosed are designs and methods of construction for an implantable medical device employing an internal support structure. The single-piece support structure holds various electronic components such as a communication coil and a circuit board, and further is affixed to a battery, thus providing a subassembly that is mechanically robust. The support structure further provides electrical isolation between these and other components. Method of construction allows for the subassembly to be adhered to a case of the implantable medical device at the battery, and possibly also at the support structure. The battery includes an insulating cover having holes. An adhesive is used consistent with the location of the holes to affix the battery to the case without electrically shorting the battery to the case. | 2015-03-05 |
| 20150066116 | Blanket - A wellness and/or heat blanket has autonomous, optically conductive fibers which are present in a proportion of 40 g/m | 2015-03-05 |
| 20150066117 | THERMOTHERAPY DEVICE - A thermotherapy device for treatment of neonates has a bordered lying surface ( | 2015-03-05 |
| 20150066118 | Intravascular Neuromodulation Device Having a Spiral Track and Associated Methods - Assemblies, systems, and methods for intravascular neuromodulation include a method of positioning a treatment device and a track element at a treatment site in an artery of a human patient and transforming the track element from a delivery configuration to a deployed configuration to form a spiral-shaped track tending to be in apposition with an inner wall of the artery. The treatment device has a distally-located neuromodulation element for sliding along the spiral-shaped track. The method can also include delivering energy via the neuromodulation element across the inner wall of a renal artery to heat or otherwise electrically modulate neural fibers that contribute to renal function. | 2015-03-05 |
| 20150066119 | INFANT WARMING SYSTEMS - Infant warming systems are described herein generally comprising a temperature regulation assembly which encloses a phase change material (PCM). The temperature regulation assembly may be initially heated (or re-heated) by water contained within a heating assembly and then placed within a retaining pouch of an infant bedding. The PCM may then provide constant heat over a period of time to the infant. A control/indicator interface coupled to the regulation assembly may constantly monitor the temperature of the PCM as well as the ambient temperature to provide one or more indications or alerts to the user with respect to one of several states of the warming assembly. | 2015-03-05 |
| 20150066120 | METHODS OF MAKING SEGMENTED ELECTRODE LEADS USING FLANGED CARRIER - A method of making a stimulation lead includes providing a carrier with a body having a first surface, a distal end, and a proximal end. The carrier also includes flanges and each flange has a leg portion attached to the body and extending away from the first surface at a non-zero angle. The method further includes attaching segmented electrodes to the first surface of the carrier; attaching conductors to the segmented electrodes; forming the carrier into a cylinder with the cylinder defining a central longitudinal axis through a center of the cylinder with the segmented electrodes disposed within the cylinder and the leg portions of the flanges extending toward the central longitudinal axis of the cylinder; molding a lead body around the segmented electrodes disposed on the carrier and around the flanges; and removing at least a portion of the carrier to separate the segmented electrodes. | 2015-03-05 |
| 20150066121 | SYSTEMS AND METHODS FOR MAKING AND USING LEAD ANCHORS FOR LEADS OF ELECTRICAL STIMULATION SYSTEMS - A lead anchor includes an anchor body having a pin lumen and spaced-apart lead lumens extending along an entire length of the anchor body. The pin lumen receives an anchoring pin with a diameter that is larger than a diameter of the pin lumen. The pin lumen has flexible walls that exert a radially-outward-directed force away from the anchoring pin when the anchoring pin is received by the pin lumen. The lead lumens each have flexible walls and receive a different lead body of at least one lead. The radially-outward-directed force exerted by the walls of the pin lumen when the anchoring pin is received by the pin lumen causes corresponding radially-inward-directed forces along the flexible walls of the lead lumens that retain portions of the lead bodies within the anchor body when the portions of the lead bodies are received by the lead lumens. | 2015-03-05 |
| 20150066122 | LEADS WITH ELECTRODES DISPOSED IN MESH MATERIAL AND METHODS AND SYSTEMS USING THE LEADS - An electrical stimulation lead has a distal end portion, a proximal end portion, and a longitudinal length and includes a lead body extending along the lead. The lead body includes an expandable mesh disposed along the distal end portion of the lead. The electrical stimulation lead also includes a number of electrodes attached to the mesh and a number of terminals disposed along the proximal end portion of the electrical stimulation lead. Further, the electrical stimulation lead includes multiple conductors electrically coupling the terminals to the electrodes. | 2015-03-05 |
| 20150066123 | NERVE CUFF WITH POCKET FOR LEADLESS STIMULATOR - An extravascular nerve cuff that is configured to hold a leadless, integral, implantable microstimulator. The nerve cuff may include a cuff body having a pocket or pouch for removably receiving the implantable device within. The nerve cuff can be secured around the nerve such that the electrodes of the device are stably positioned relative to the nerve. Furthermore, the nerve cuff drives the majority of the current from the stimulation device into the nerve, while shielding surrounding tissues from unwanted stimulation. | 2015-03-05 |
| 20150066124 | FILTER CIRCUIT FOR AN ACTIVE IMPLANTABLE MEDICAL DEVICE - A shielded three-terminal flat-through EMI/energy dissipating filter includes an active electrode plate through which a circuit current passes between a first terminal and a second terminal, a first shield plate on a first side of the active electrode plate, and a second shield plate on a second side of the active electrode plate opposite the first shield plate. The first and second shield plates are conductively coupled to a grounded third terminal. In preferred embodiments, the active electrode plate and the shield plates are at least partially disposed with a hybrid flat-through substrate that may include a flex cable section, a rigid cable section, or both. | 2015-03-05 |
| 20150066125 | TEMPORARILY IMPLANTABLE ELECTRODE ASSEMBLY FOR THE STIMULATION AND INTRACARDIAC CARDIOVERSION/DEFIBRILLATION OF THE HEART FOLLOWING SURGERY - The invention relates to an electrode assembly for temporary cardioversion/defibrillation and/or for temporary stimulation of the heart after open heart surgery consisting of two defibrillation electrodes with at least one indifferent pole each and an elastic section, where each defibrillation electrode in the operating position is positioned on the right and left atrium, which means the defibrillation electrodes together include the right and left atrium. The defibrillation electrodes each distally comprise a fixation member and each proximally end into a protective tube to protect the epicardium. The fixation members are elastic and enable reversible fastening of the defibrillation electrodes in the pericardium on the right and left side. The protective tubes are preferably fed together into a guide tube, where the guide tube is slidable along the longitudinal axis. The stimulation electrodes (different electrode poles) for stimulation of the atria are designed appropriately together with the defibrillation electrode in one piece. | 2015-03-05 |
| 20150066126 | Fenestration Electrode to Treat Patients with Meniere's Disease - An implantable fenestration electrode delivers electrical stimulation signals for treatment of Meniere's disease. An electrode lead contains one or more signal wires for carrying a stimulation signal. An electrode tip at a terminal end of the electrode lead is configured for placement within a fenestration opening in an outer surface of a bony labyrinth of a patient with Meniere's disease without penetrating or impairing intra-labyrinthine membranes or neural tissue, and is adapted to deliver the stimulation signal via intra-labyrinthine fluid to the intra-labyrinthine neural tissue. | 2015-03-05 |
| 20150066127 | DELIVERY OF MEDICAL DEVICES - A stent delivery system can include an elongate core member sized for insertion into a blood vessel. The core member can be configured to advance a stent toward a treatment location in the blood vessel. The core member can include a longitudinally extending tube having a helical cut extending along the tube. The helical cut can have an axial length of at least 50 cm and be continuous along the axial length. | 2015-03-05 |
| 20150066128 | DELIVERY OF MEDICAL DEVICES - A stent delivery system can include a core member and a stent. The stent can be carried by an intermediate portion of the core member. The core member can have an elongate, spiral-cut tube extending proximally of the intermediate portion. The core member can have one or more flex zones having different bending stiffnesses. | 2015-03-05 |
| 20150066129 | DELIVERY OF MEDICAL DEVICES - A stent delivery system can include a core member, a stent engagement member, and a stent. The core member can have a distal segment. The stent engagement member can have a generally tubular body positioned about the core member distal segment and can be rotatably coupled to the core member. The engagement member can include an inner layer that has a first durometer and an outer layer that has a second durometer less than the first durometer. The stent can extend along the core member distal segment such that an inner surface of the stent is engaged by the engagement member outer layer for facilitating rotation of the stent relative to the core member. | 2015-03-05 |
| 20150066130 | DELIVERY OF MEDICAL DEVICES - A stent delivery system can include a core member, an introducer sheath, and a microcatheter. The core member can have a first section and a second section distal to the first section. The second section can have a bending stiffness per unit length that is less than a bending stiffness per unit length of the first section. The introducer sheath can have a lumen configured to receive the core member therethrough. The introducer sheath can have a length of at least about 80 cm. The microcatheter can have a lumen and a proximal end configured to interface with a distal end of the introducer sheath for delivering the core member into the microcatheter lumen. | 2015-03-05 |
| 20150066131 | DELIVERY OF MEDICAL DEVICES - A stent delivery system can include a core member, a stent, and a stent engagement member. The engagement member can be positioned along a distal segment of the core member and be coupled to the core member. The engagement member can have an outer surface. The stent can extending along the core member distal segment such that the outer surface of the engagement member engages an inner surface of the stent along at least a portion of only a distal half of the stent for transmitting an axial force from the core member to only the stent distal half of the stent. | 2015-03-05 |
| 20150066132 | BALLOON CATHETER AND STENT DELIVERY SYSTEM - A balloon catheter is disclosed, which includes an elongated shaft body, a dilatable balloon in which a distal end portion and a proximal end portion form a dilation chamber inside of the dilatable balloon by being away from each other and being individually bonded to an outer periphery of the shaft body, and a stretch regulation member that connects the outer periphery of the shaft body or an inner periphery of the balloon of the distal end portion of the balloon and the outer periphery of the shaft body or the inner periphery of the balloon of the proximal end portion of the balloon with each other inside the dilation chamber while regulating a stretch occurring between the distal end portion and the proximal end portion of the balloon during dilation of the balloon. | 2015-03-05 |
| 20150066133 | Intraluminal Prostheses Having Polymeric Material With Selectively Modified Crystallinity - Methods of manufacturing polymeric intraluminal prostheses include annealing the polymeric material to selectively modify the crystallinity thereof. Annealing may be utilized to selectively modify various properties of the polymeric material of an intraluminal prosthesis, including: selectively increasing the modulus of the polymeric material; selectively increasing the hoop strength of the intraluminal prosthesis; selectively modifying the elution rate (increase or decrease) of a pharmacological agent subsequently disposed on or within the annealed polymeric material; selectively increasing/decreasing stress in the intraluminal prosthesis; and selectively modifying the polymeric material such that it erodes at a different rate. | 2015-03-05 |
| 20150066134 | MULTI-LAYERED STENTS AND METHODS OF IMPLANTING - A method of percutaneously delivering a multi-layered stent assembly to a desired implantation location of a patient including the steps of radially compressing a multi-layered stent assembly to a compressed size for implantation in a patient, the multi-layered stent assembly including a first stent, a second stent coaxially positioned within at least a portion of a length of the first stent, and a valve, wherein the first stent comprises at least one different material property than the second stent. The method further includes delivering the multi-layered stent assembly to the desired implantation location of the patient using a delivery system and substantially simultaneously expanding the first stent and the second stent of the multi-layered stent assembly at the desired implantation location to a radially expanded size that is larger than the compressed size. | 2015-03-05 |
| 20150066135 | Bioerodible Composites for Endoprostheses - A bioerodible endoprosthesis includes a composite including a matrix comprising a bioerodible magnesium alloy and a plurality of ceramic nanoparticles within the matrix. The bioerodible magnesium alloy has a microstructure including equiaxed Mg-rich solid solution-phase grains having an average grain diameter of less than or equal to 5 microns. The microstructure can be produced by one or more equal-channel high-strain processes. | 2015-03-05 |
| 20150066136 | Anchoring Studs for Transcatheter Valve Implantation - An anchoring device for use within a vascular structure includes a head having a first surface and a second surface meeting at a common plane, and an anchor including a shaft having a longitudinal axis, a first end connected at a junction to the first surface of the head, and a free end. A harbor space is bounded by the shaft of the anchor, the first surface of the head, a first theoretical plane perpendicular to the longitudinal axis at a spaced distance from the junction and a second theoretical plane tangential to the head at a point in the common plane. The harbor space has an are sufficient to receive a portion of a stented device therein. | 2015-03-05 |
| 20150066137 | INTEGRATED BALLOON CATHETER INFLATION SYSTEM - An inflation system having two pressure vessels integrated into a balloon catheter. A pressurized chamber and a vacuum chamber are integrally attached to proximal end of the balloon catheter and activated by a common valve or switch. Pressure or vacuum is selectively transmitted to the balloon depending on the valve/switch position. The working fluid may be air, or a combination of air and saline with an intermediate piston/cylinder assembly. The balloon catheter may be a part of a heart valve delivery system with a balloon-expandable heart valve crimped onto the balloon. | 2015-03-05 |
| 20150066138 | Devices and Methods for Locating and Implanting Tissue Anchors at Mitral Valve Commissure - The present teachings provide devices and methods of locating a mitral valve commissure, and implanting tissue anchors at or near the mitral valve commissure. Specifically, one aspect of the present teachings provides devices and methods for locating a mitral valve commissure percutaneously and allowing a guide wire to be placed across a mitral annulus at the mitral valve commissure. Another aspect of the present teachings provides methods for deploying a tissue anchor across a mitral annulus at a mitral valve commissure, including near the P1 or P3 regions of the posterior mitral annulus. Another aspect of the present teachings further provides methods of plicating a mitral annulus between two or more tissue anchors. | 2015-03-05 |
| 20150066139 | HEART ANCHOR POSITIONING DEVICES, METHODS, AND SYSTEMS FOR TREATMENT OF CONGESTIVE HEART FAILURE AND OTHER CONDITIONS - According to one embodiment, a heart anchor tensioning device includes a main body and an elongate shaft. A tension member or tether may be inserted through a lumen of the elongate shaft to allow the shaft to be advanced over the tension member and within a body while the main body is positioned outside of the body. The device also includes an anchor coupling mechanism that is configured to engage a heart anchor and move the heart anchor into engagement with a first wall of the heart. The anchor coupling mechanism is able to lock the heart anchor to inhibit proximal movement of the heart anchor along the tension member. The device further includes a tension indicating mechanism that provides an indication of a force being applied to the heart anchor by the device. | 2015-03-05 |
| 20150066140 | VASCULAR IMPLANT AND DELIVERY METHOD - A vascular implant for replacing a native heart valve comprises a self expanding stent supporting a valve body having leaflets. The stent preferably comprises an anchoring structure configured to prevent the implant from passing through the valve annulus. For delivery, the implant is compacted within a delivery device and secured at one end. During delivery the implant is partially released from the delivery device, and positioning of the implant can be verified prior to full release. The implant can be at least partially resheathed and repositioned if desired. | 2015-03-05 |
| 20150066141 | COMMISSURE ATTACHMENT FEATURES FOR IMPROVED DELIVERY FLEXIBILITY AND TRACKING - A prosthetic heart valve includes a collapsible and expandable stent having a proximal end and a distal end. A plurality of commissure attachment features (“CAFs”) is disposed on the stent, with each CAF including a body and a plurality of eyelets. The eyelets may be arranged in a single column or in a plurality of rows and columns. The prosthetic heart valve also includes a collapsible and expandable valve assembly including a plurality of leaflets connected to the plurality of commissure attachment features. The bodies of the CAFs may include a number of other features including, for example, a slot extending between columns of eyelets. | 2015-03-05 |
| 20150066142 | Four Chamber Redundant-Impeller Artificial Heart - An artificial heart for use in a human recipient includes a housing within which a quartet of turbine pump segments are operative. The quartet of turbine pump segments provides a redundancy which in turn enhances the safety factor provided by the artificial heart. A controller is powered by a rechargeable battery and is operative to apply appropriate drive signals to the motor drives of the turbine pump segments. The battery may be implanted along with the controller to avoid the need for any external connections to the artificial heart. An inductively coupled battery charger for use outside the recipient's body is positioned proximate the battery charger to provide inductively coupled charging for use in driving the artificial heart. | 2015-03-05 |
| 20150066143 | Silicone Filamentous Configurations - This novel solid silicone device is designed to let women have more and better choices in breast implant technology for both cosmetic and reconstructive purposes, include shape filling and solid devices overcoming longstanding needs. | 2015-03-05 |
| 20150066144 | Implant Made of a Fiber Composite Material - The invention relates to an implant and a set for producing an implant and their uses. Furthermore, the invention describes a method of making an implant as per the invention. An implant for producing bone implants with improved mechanical characteristics, especially with adjustable mechanical characteristics, is provided via the invention. The implant as per the invention made up of a fiber composite material contains
| 2015-03-05 |
| 20150066145 | EXPANDABLE AND ADJUSTABLE LORDOSIS INTERBODY FUSION SYSTEM - An expandable housing for an interbody fusion system has movable tapered external helical threaded members that travel along tracking to operably engage against the top and bottom shell members, urging them apart to cause expansion in the height of the housing. In an embodiment, the tapered members are disposed in a dual arrangement such that independent engagement of the tapered members along lateral portions of the top and bottom shells cause an angular tilt to the exterior surface of the housing when the tapered members are moved to different degrees. This function permits adjustment in the angular relationship between adjacent vertebrae and assists the lordotic adjustment of the patient's spine. When the functions of the device are used in combination by the surgeon, the device provides an effective tool for in situ adjustment when performing lateral lumbar interbody fusion. | 2015-03-05 |
| 20150066146 | PROSTHESIS, SYSTEM AND METHOD - An implant device, system and method can include a top structure, a bottom structure, and an intermediary structure. The bottom structure can include a helical groove structure, and the intermediary structure can include at least one pin that cooperates with the helical groove structure such that the pin and the helical groove structure guide the intermediary structure in both a rotational direction about the central axis and an axial linear direction along the central axis. The bottom structure can also include a linear groove structure configured to guide the top structure in a linear motion with respect to the bottom structure when the intermediary structure is rotated with respect to the bottom structure. | 2015-03-05 |
| 20150066147 | INTERBODY VERTEBRAL PROSTHETIC AND ORTHOPEDIC FUSION DEVICE WITH SELF-DEPLOYING ANCHORS - An intervertebral prosthesis includes: a body; at least three apertures extending from within the body; at least three anchoring elements disposed within the at least three apertures; and a drive mechanism operating to simultaneously push the at least three anchoring elements out through the apertures, where: a first deployment direction of a first of the anchoring elements includes: (i) a first substantial directional component in one of an anterior and posterior direction of the body; and (ii) a second substantial directional component parallel to the longitudinal axis of the body; a second deployment direction of a second of the anchoring elements includes: (i) a first substantial directional component in one of an anterior and posterior direction of the body; and (ii) a second substantial directional component parallel to the longitudinal axis of the body and opposite to the second substantial directional component of the first deployment direction of the first anchoring element; and the drive mechanism operates to move the first anchoring element at least some distance in the first deployment direction and to move the second anchoring element at least some distance in the second deployment direction. | 2015-03-05 |
| 20150066148 | Intervertebral Implant Facilitating Unilateral Placement, Instruments and Methods - Implants, tools and methods for performing unilateral posterior lumbar interbody fusion are provided. An interbody implant includes a body having a top and bottom surface extending along a length thereof; and first and second side surfaces extending between the top and bottom surfaces on opposite sides of the body. The height of the first side surface is greater than the height of the second side surface. | 2015-03-05 |
| 20150066149 | EXTENDED ARTICULAR SURFACE RESURFACING HEAD - A modular humeral head resurfacing implant including a head, an anchoring stem, and a modular extended articulation flange. The head includes an exterior hemispherical articulating surface defining a terminating rim, an interior concave surface opposite to the exterior articulating surface, and a first coupling mechanism proximate to the terminating rim. The anchoring stem is coupled to the interior concave surface and extends along a stem axis that extends through an axial center of the head. The articulation flange includes a second coupling mechanism configured to cooperate with the first coupling mechanism to fasten the articulation flange to the head and an outer articulating surface that is curved along substantially its entire length and is substantially flush with the exterior hemispherical articulating surface when the articulation flange is fastened to the head. | 2015-03-05 |
| 20150066150 | METHOD FOR OPTIMIZING IMPLANT DESIGNS - Methods are disclosed for designing a tibial implant to minimize cortical impingement of a keel or other fixation structure when the tibial implant is implanted in the tibia bone. The design of the keel or other fixation structure on the tibial baseplate can be based on determining a common area between defined cancellous regions of at least two tibia bones. Methods are disclosed for designing a femoral component having a stem extension such that the stem can be sufficiently placed in the diaphysis of the femur when the femoral component is implanted. The method includes determining a canal axis in a femur that creates adequate engagement between a reamer and the diaphysis of the femur. | 2015-03-05 |
| 20150066151 | METHODS AND APPARATUS FOR FAI SURGERIES - A partial rim implant for an acetabulum in a pelvic bone comprises a ridge, a bearing surface, and a fixation surface. The ridge is oriented to replace a labrum. The bearing surface is configured to align with the articulating surface of the acetabulum. The bearing surface extends from the ridge toward the apex of the acetabulum. The fixation surface is configured to fix the implant to a prepared bone surface of the pelvic bone. | 2015-03-05 |
| 20150066152 | Orthopaedic Joints Providing Enhanced Lubricity - The present disclosure provides, among other things, prosthetic joint components having textured surface(s) for improving lubrication and increasing the useful life of the prosthetic joint components. The textured surface includes solid features configured to stably contain a biological fluid or a synthetic biological fluid therebetween or therewithin for a non-zero residence time. | 2015-03-05 |
| 20150066153 | MICROPROCESSOR CONTROLLED PROSTHETIC ANKLE SYSTEM FOR FOOTWEAR AND TERRAIN ADAPTATION - A prosthetic ankle includes a pair of prosthetic members movably coupled together to allow movement of the pair of prosthetic members with respect to one another. A hydraulic actuator or damper including hydraulic fluid in a hydraulic chamber is coupled to one of the pair of prosthetic members. A hydraulic piston is movably disposed in the hydraulic chamber and coupled to another of the pair of prosthetic members. A hydraulic flow channel is fluidly coupled between opposite sides of the chamber to allow hydraulic fluid to move between the opposite sides of the chamber as the hydraulic piston moves therein. A voice coil valve is coupled to the hydraulic flow channel to vary resistance to flow of hydraulic fluid through the flow channel, and thus movement of the piston in the chamber, and thus influencing a rate of movement of the pair of prosthetic members with respect to one another. | 2015-03-05 |
| 20150066154 | MICROPROCESSOR CONTROLLED PROSTHETIC ANKLE SYSTEM FOR FOOTWEAR AND TERRAIN ADAPTATION - A prosthetic ankle includes a pair of prosthetic members movably coupled together to allow movement of the pair of prosthetic members with respect to one another. A hydraulic actuator or damper including hydraulic fluid in a hydraulic chamber is coupled to one of the pair of prosthetic members. A hydraulic piston is movably disposed in the hydraulic chamber and coupled to another of the pair of prosthetic members. A hydraulic flow channel is fluidly coupled between opposite sides of the chamber to allow hydraulic fluid to move between the opposite sides of the chamber as the hydraulic piston moves therein. A voice coil valve is coupled to the hydraulic flow channel to vary resistance to flow of hydraulic fluid through the flow channel, and thus movement of the piston in the chamber, and thus influencing a rate of movement of the pair of prosthetic members with respect to one another. | 2015-03-05 |
| 20150066155 | WIRELESS CHARGING FOR PROSTHETIC DEVICE - A prosthetic device including a power storage unit to power the prosthetic device and an electromagnetic receiver including a plurality of coils arranged about a portion of the prosthetic device. The electromagnetic receiver is configured to receive a magnetic field from an electromagnetic transmitter magnetically coupled with the electromagnetic receiver and to generate electric power from the magnetic field. Circuitry of the prosthetic device stores the electric power generated from the magnetic field in the power storage unit. The electromagnetic transmitter includes circuitry configured to receive power from a power supply and a plurality of coils configured to generate the magnetic field using the electric power. | 2015-03-05 |
