| 19th week of 2013 patent applcation highlights part 51 |
| Patent application number | Title | Published |
|---|
| 20130116699 | Patient-Specific Femoral Version Guide - An orthopedic device includes a monolithic patient-specific guide. The patient-specific guide includes a three-dimensional contact surface preoperatively configured from medical scans of a specific patient as a negative surface of a medial portion of a proximal femoral bone of the patient according to a preoperative surgical plan for the patient. The guide also includes a proximal planar surface configured for guiding a resection of a femoral neck of the patient, and a scale formed on the planar surface. The scale is configured for indicating a preoperatively planned femoral version of a femoral stem implant and deviations therefrom. | 2013-05-09 |
| 20130116700 | SCREW GUIDE TEMPLATE, SCREW GUIDE TEMPLATE SYSTEM, DRILLING METHOD, AND SPINAL FIXATION METHOD - Provided are: a screw guide template, screw guide template system, and drilling method whereby a hole can be drilled in an accurate position of a member to be drilled, in an accurate direction; and a spinal fixation method whereby a spinal fixation screw can be inserted into an accurate position in an accurate direction. The screw guide template ( | 2013-05-09 |
| 20130116701 | GUIDE EXTENSION CATHETER - Medical devices and methods for making and using medical devices are disclosed. An example medical device may include a guide extension catheter. The guide extension catheter may include a proximal tubular member having a lumen defined therein. A distal tubular member may be attached to the proximal tubular member. The proximal tubular member may have an outer diameter. The distal tubular member may have an inner diameter. The inner diameter of the distal tubular member may be greater than the outer diameter of the proximal tubular member. A stiffening member may be slidably disposed within the proximal tubular member. | 2013-05-09 |
| 20130116702 | Flexible Vacuum Grabber for Holding Lesions - A grabbing device includes a transparent flexible cup that can be placed adjacent to a selected region of an inner surface of a body cavity. The flexible cup is visually put in place by the surgeon, and a vacuum is applied to draw a selected amount of tissue into the flexible cup, so that it may, e.g., be excised. The device may also retrieve the tissue excised from the body cavity. | 2013-05-09 |
| 20130116703 | Apparatus for Using Hydrodynamic Cavitation in Medical Treatment - An apparatus for using hydrodynamic cavitation in medical treatment such as destroying kidney stones or killing infected cancer cells. This apparatus comprises a tank used as a container for a fluid, a compressor connected to the tank to maintain the input pressure of the fluid, a tubing wherein the fluid flows, a probe in which the cavitation occurs, a valve positioned inside the tubing, allowing the fluid to flow into the probe, a filter positioned inside the tubing, preventing the predetermined size particles flowing into the probe, a fitting connecting the probe to the tubing, a flowmeter measuring the volume flow rate of the fluid through the probe, an image capturing unit capturing the sequential images of bubbles growing and bubbles collapsing after the bubbles exit from the probe, a positioning assembly which adjusts the distance between the probe and the target surface, and a control and data acquisition unit. | 2013-05-09 |
| 20130116704 | Device for Explanting Electrode Leads - An explantation device for explanting implanted leads, having a distal end pointing in the direction of the explantation site and a proximal end pointing in the direction of the surgeon. The explantation tool comprising a locking sheath comprising a hose-like or tubular body having a lumen along a longitudinal axis and at least one clamping device at or in the vicinity of the distal end; and a cutting sheath for removing adhering tissue, having a proximal and a distal end and comprising a hose-like or tubular body having a lumen along a longitudinal axis and a detaching unit at or in the vicinity of the distal end; wherein the cutting sheath comprises at least one receptacle for the clamping device of the locking sheath. | 2013-05-09 |
| 20130116705 | Steerable Delivery Sheaths - Steerable medical delivery devices and their methods of use. | 2013-05-09 |
| 20130116706 | SURGICAL ROBOT AND CONTROL METHOD THEREOF - A method for controlling a surgical robot includes calculating an external force acting on a robot arm mounted with a surgical instrument, filtering the external force acting on the robot arm when a central point of an incision is set, calculating a virtual force to enable the surgical instrument which is positioned away from the central point of the incision to return to the central point of the incision, and applying the calculated virtual force to the filtered external force, to control movement of the robot arm. As a result, it is possible to compactly design the surgical robot and thereby reduce the volume of the surgical robot. | 2013-05-09 |
| 20130116707 | ROBOT STRUCTURE - A robot structure, in particular for minimally invasive surgery, is provided with a first robot element and a second robot element that can be moved relative to the first robot element, said second robot element having two grasping and/or cutting elements which can be uniformly moved with respect to each other and which are connected to the first robot element via a hinge axis. The robot structure further has a force transmitting device for moving the grasping and/or cutting elements of the movable robot element and at least one sensor element comprising a sensitive end for receiving forces and/or torques that occur on the movable robot element and includes a base element that is fixed to the first robot element. | 2013-05-09 |
| 20130116708 | INSTRUMENTS FOR DELIVERING TRANSFASCIAL SUTURES AND METHODS OF TRANSFASCIAL SUTURING - An instrument for delivering a suture transfascially may include a handle, a shaft extending from the handle, and at least one needle that is moveable to an extended position beyond the end of the shaft. A suture may be delivered transfascially with the instrument. The instrument may include a suture catch associated with each needle for retaining and releasing a suture segment. A shield may be provided to shield the sharp end of each needle when it is moved to the extended position. A method of delivering a transfascial suture may include inserting an instrument into an abdominal cavity and deploying, from within the abdominal cavity, each needle through a soft tissue repair patch and then through at least part of the to abdominal wall. A suture or suture segment may be advanced across the fascia with the at least one needle. | 2013-05-09 |
| 20130116709 | INSTRUMENTS FOR DELIVERING TRANSFASCIAL SUTURES AND METHODS OF TRANSFASCIAL SUTURING - An instrument for delivering a suture transfascially may include a handle, a shaft extending from the handle, and at least one needle that is moveable to an extended position beyond the end of the shaft. A suture may be delivered transfascially with the instrument. The instrument may include a suture catch associated with each needle for retaining and releasing a suture segment. A shield may be provided to shield the sharp end of each needle when it is moved to the extended position. A method of delivering a transfascial suture may include inserting an instrument into an abdominal cavity and deploying, from within the abdominal cavity, each needle through a soft tissue repair patch and then through at least part of the abdominal wall. A suture or suture segment may be advanced across the fascia with the at least one needle. | 2013-05-09 |
| 20130116710 | INSTRUMENTS FOR DELIVERING TRANSFASCIAL SUTURES AND METHODS OF TRANSFASCIAL SUTURING - An instrument for delivering a suture transfascially may include a handle, a shaft extending from the handle, and at least one needle that is moveable to an extended position beyond the end of the shaft. A suture may be delivered transfascially with the instrument. The instrument may include a suture catch associated with each needle for retaining and releasing a suture segment. A shield may be provided to shield the sharp end of each needle when it is moved to the extended position. A method of delivering a transfascial suture may include inserting an instrument into an abdominal cavity and deploying, from within the abdominal cavity, each needle through a soft tissue repair patch and then through at least part of the abdominal wall. A suture or suture segment may be advanced across the fascia with the at least one needle. | 2013-05-09 |
| 20130116711 | SILK BASED IMPLANTABLE MEDICAL DEVICES AND METHODS FOR DETERMINING SUITABILITY FOR USE IN HUMANS - 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 can maintain at least 90% of its time zero strength at one month in vivo after implantation. The silk scaffold can maintain at least 90% of its time zero strength over a multi-month period in vivo after implantation. | 2013-05-09 |
| 20130116712 | APPARATUS AND METHOD FOR ENDOSCOPIC COLECTOMY - Apparatus and methods for endoscopic colectomy are described herein. A colectomy device having a first and a second tissue approximation device is mounted on a colonoscope separated from one another. During deployment of the colectomy device, a diseased portion of the colon is positioned inbetween the tissue approximation devices. The tissue approximation devices are radially expanded such that they contact and grasp the colon wall at two sites adjacent to the diseased portion of the colon. The diseased portion is separated from the omentum and is transected using a laparoscope or is drawn into the colonoscope for later removal. The tissue approximation devices are then urged towards one another over the colonoscope to approximate the two free edges of the colon into contact together where they are fastened to one another using the tissue approximation device as a surgical stapler to create an end-to-end anastomosis. | 2013-05-09 |
| 20130116713 | DEVICES AND RELATED METHODS FOR SECURING A TISSUE FOLD - The present invention relates to devices and methods for creating and securing a tissue fold during an endoluminal medical procedure. The devices and methods may be used for folding and securing, for example, a fundus wall onto an esophagus wall. An aspect of the invention includes a two-piece tissue clip configured to be installed through an endoluminal device to secure a tissue fold. The clip includes a female member and a male member configured to engage one another to secure the tissue fold. Another aspect of the invention includes a clipping device comprising a tissue clip magazine. The magazine is configured to hold a plurality of tissue clips and install the plurality of tissue clips in a single actuation of the magazine. A method for using the clipping device together with the tissue clips of the present invention to create and secure a fold of tissue during an endoluminal procedure also is disclosed. | 2013-05-09 |
| 20130116714 | SHOCK WAVE VALVULOPLASTY DEVICE WITH MOVEABLE SHOCK WAVE GENERATOR - A valvuloplasty system comprises a balloon adapted to be placed adjacent leaflets of a valve. The balloon is inflatable with a liquid. The system further includes a shock wave generator within the balloon that produces shock waves that propagate through the liquid for impinging upon the valve. The shock wave generator is moveable within the balloon to vary shock wave impingement on the valve. | 2013-05-09 |
| 20130116715 | MEDICAL CUTTING DEVICES AND METHODS OF USE - A cutting device for repairing a heart valve may include a delivery catheter, a cutting unit including an elongate shaft and a plurality of cutting wires, and a plurality of centralizing wires configured to center the cutting unit within a treatment site. A method of repairing a heart valve may include withdrawing a cutting unit through a treatment site while maintaining a plurality centralizing wires in an expanded centering configuration. | 2013-05-09 |
| 20130116716 | LIQUID-JET SCALPEL - A liquid-jet scalpel for minimally invasive surgery, comprising a nozzle for ejecting a liquid jet, and a functional end effector for manipulating tissue at the surgical site. | 2013-05-09 |
| 20130116717 | ULTRASONIC DEVICE FOR CUTTING AND COAGULATING - An ultrasonic assembly that is configured to permit selective cutting, coagulation, and fine dissection required in fine and delicate surgical procedures. The balanced blade provides a rounded distal end and concave edges to promote fine dissection and cutting in a variety of surgical procedures. The blade is curved for improved visibility at the blade tip and is designed to provide a multitude of tissue effects: coagulation, cutting, dissection, spot coagulation, tip penetration and tip scoring. The assembly features hand activation configured to provide an ergonomical grip and operation for the surgeon. The assembly further features user selectable blade rotation. A finger switch is placed in the range of the natural axial motion of the user's index finger, whether gripping the surgical instrument right-handed or left handed. | 2013-05-09 |
| 20130116718 | LANCET - The invention relates to a lancet, which has a lancet tip at a front end and which on an upper face comprises a contact surface for placing a test element thereon and at least one channel for receiving a sample, wherein an upwardly open section of the channel runs in the contact surface. According to the invention, the channel has another upwardly open channel section which runs on the upper face of the lancet in or adjacent to a surface area that is lower than the contact surface, wherein the contact surface is arranged between the lancet tip and the lower surface area. The invention further relates to a system comprising such a lancet and a test element, and to a method for transferring a liquid sample from a channel of a lancet which is designed as a groove or slot to a test element. | 2013-05-09 |
| 20130116719 | LANCING DEVICE WITH INTEGRATED THERMOELECTRIC COOLER - A lancing device (e.g., pen) having an integrated thermoelectric (e.g., Peltier) cooler. The lancing device includes an elongated heat accumulator having a lumen along which a piston having a lancet thereon translates back and forth. A Peltier device and a cooling ring are thermally interconnected to one end of the heat accumulator and include central apertures through which the lancet can extend. The lancing device also includes an integrated battery and microcontroller for supplying and regulating power to the Peltier device. Upon a current being sent through the Peltier device, a cold side of the Peltier device and hence the cooling ring gives up thermal energy and reduces in temperature. The cooling ring can then be placed about a body tissue (e.g., skin) for a period of time (e.g., 3-5 seconds) to desensitize the body tissue, and then the lancet can be fired to puncture the body tissue. | 2013-05-09 |
| 20130116720 | Multi-stage Occlusion Devices - An occlusion device has a covering attached to a support frame that includes a disc-shaped member and a crossbar that extends across a central opening defined by the disc-shaped member. The occlusion device has a first, or deployed, configuration in which the crossbar defines a curve that extends from the disc-shaped member, and a second, or resting, configuration in which the disc-shaped member and the crossbar lie substantially in a single plane. Each of the disc-shaped member and the crossbar include a core wire that extends through a lumen of a coil multiple times. | 2013-05-09 |
| 20130116721 | Medical Device - A medical device configured to provide a space, allowing a medical instrument to move, in an area of the brain in which the medical instrument is otherwise difficult to move. The medical device includes a catheter provided with an expandable member, wherein the expandable member is expanded to provide a space in which at least a part of a second medical instrument is insertable and movable. | 2013-05-09 |
| 20130116722 | DEVICES AND METHODS FOR THE TREATMENT OF VASCULAR DEFECTS - Devices and methods for treating vascular defects, such as, for example, balloon-type aneurysms, are described herein. In one embodiment, an apparatus includes an insertion portion and an expandable implant. The expandable implant is configured to be deployed in an aneurysm and is coupled to the insertion portion. The expandable implant has a first portion and a second portion coupled to the first portion. The expandable implant is movable between a first configuration in which the first portion and the second portion are substantially linearly aligned and a second configuration in which the second portion at least partially overlaps the first portion. | 2013-05-09 |
| 20130116723 | DETACHMENT MECHANISM FOR A CENTRAL VENOUS ACCESS FILTER AND METHOD OF USE - A detachment and retrieval mechanism for a central venous access filter includes a catheter body, and an outer sheath concentrically disposed about the catheter body. The outer sheath and the catheter body are moveable relative to one another. A filter member includes a first end coupled to the catheter body and a second end movable relative to the catheter body. | 2013-05-09 |
| 20130116724 | HANDLE ASSEMBLY FOR A LEFT ATRIAL APPENDAGE OCCLUSION DEVICE - The disclosure pertains to a handle assembly for a left atrial appendage occlusion device delivery system and methods of use therefor. The handle assembly includes a leadscrew mechanism for smooth, low backlash control of a delivery catheter for the left atrial appendage occlusion device and manipulation segments which allow one hand operation of the handle assembly. | 2013-05-09 |
| 20130116725 | METHOD TO STOP BLEEDING AT A PUNCTURE SITE OF AN ARTERY OF A PATIENT'S WRIST - A method to stop bleeding at a puncture site of an artery on a wrist of a patient comprises wrapping a flexible band of a hemostatic device around the wrist of the patient, wherein the hemostatic device also includes a curved plate, a balloon and a marker used to position the balloon at the puncture site, and wherein the flexible band, the curved plate and the balloon are substantially transparent. The wrapping of the flexible band around the wrist of the patient involves wrapping the flexible band around the wrist of the patient while the balloon is in an uninflated state. The wrapping can also take place while an introducer sheath is in place at the puncture site. The method also involves using the marker to position balloon relative to the puncture site such that the balloon overlies the puncture site, introducing a fluid into the balloon and inflating the balloon, and maintaining inflation of the balloon and compression against the puncture site. | 2013-05-09 |
| 20130116727 | Nasal Support Device and Method - The present disclosure provides a device and method for facilitating air flow in the nasal passage of a domestic animal. The nasal support device (NSD) disclosed herein is useful for facilitating air flow during rest, physical exertion, respiratory ailment, etc. The NSD secures to the nose of a domestic animal to support the unsupported lateral vestibular walls of the nasal passages by lifting or stenting. | 2013-05-09 |
| 20130116728 | SYSTEM AND METHOD FOR TRANSAPICAL ACCESS AND CLOSURE - Embodiments are described for creating and closing tissue access ports, such as transapical access ports, which involve placement of an introducer across the subject tissue structure, and deployment of a controllable port closure device assembly configured to remain in place with a ratcheting mechanism, and to hold the tissue surrounding the previous access port location closed against a sealing disc with proximal and distal strut assemblies, after the introducer has been removed. | 2013-05-09 |
| 20130116729 | INTRAVASCULAR HEMOSTASIS-TYPE CATHETER - When the intravascular hemostasis-type catheter is inserted into a blood vessel, an elastically deformable portion is formed into a deflated shape and accommodated in a first lumen of the catheter body. When the top end of the catheter body reaches near a damaged blood vessel wall, the shaft is inserted into the catheter body, and then the elastically deformable portion is pushed out from the first lumen of the catheter body to elastically return to an inflated shape from the deflated shape, so that the hemostatic film presses the damaged blood vessel wall. Therefore, hemostasis can be performed in blood vessels following various sizes of the blood vessels. Hemostasis can be performed in blood vessels without blocking the blood flow toward the peripheral side. | 2013-05-09 |
| 20130116730 | Method And Apparatus For Stitching Tendons - Methods and apparatuses for repairing a tear in soft tissue are disclosed. A method according to the principles of the present disclosure includes connecting an intermediate member to a bone anchor and placing the intermediate member on the soft tissue. The method further includes inserting a first suture through the intermediate member and the soft tissue to attach the intermediate member to the soft tissue and fixing the bone anchor to bone to secure the soft tissue to the bone. | 2013-05-09 |
| 20130116731 | SPINAL CROSS CONNECTORS - Various methods and devices are provided for connecting spinal fixation elements, such as spinal rods, implanted in a patient's spinal column. In particular, various spinal cross connectors are provided for connecting to one or more spinal fixation elements implanted in a patient's spine. The cross connectors can have a variety of configurations, including a fixed or adjustable length, as well as various features that allow certain portions of the cross connectors to be angularly oriented. | 2013-05-09 |
| 20130116732 | Method for Locking an Artificial Facet Between Two Vertebral Bodies - A bone screw ( | 2013-05-09 |
| 20130116733 | Bone Clamp and Method - A bone clamp and method of using the bone clamp are provided. The bone clamp includes a pair of squeeze handles. Movement of one of the handles forces a push rod in a uniaxial direction. The push rod has a moveable jaw secured to a distal end thereof. A stationary jaw is connected to the other handle member. A curved slot formed in the handle member receives the push rod and ensures a unidirectional or linearly directed force is applied to the push rod. This uniaxial force prevents shifting of the bone plate when the clamp makes contact with a bone and a bone plate. The orientation of the clamping surfaces of the jaws provide an optimal orientation to attach the bone plate to the anterior surface of a bone allowing an unimpeded view of the fracture around the superior and inferior surfaces of the bone. | 2013-05-09 |
| 20130116734 | APPARATUS AND METHOD FOR USE OF THE APPARATUS FOR FRACTURE FIXATION OF THE DISTAL HUMERUS - A system for fixing fractured bone portions of a distal humerus in position with respect to one another. In one embodiment, the system includes a plate portion, a projection portion, and a fixation post. The plate portion includes a surface for contacting a posterior portion of the distal humerus adjacent one of a lateral side and a medial side thereof. The projection portion extends outwardly from the plate portion and includes an aperture for receiving the fixation post. The fixation post includes at least one fenestration, and extends from adjacent the one of the lateral and medial sides of the distal humerus to adjacent the other of the lateral and medial sides of the distal humerus. | 2013-05-09 |
| 20130116735 | Bone Plate - A bone plate has an underside on the side of the bone, an upper side and a plurality of holes in the plate connecting the underside with the upper side, with a central hole axis. At least one of these holes in the plate has an internal jacket surface that tapers towards the underside, while the internal jacket surface has N≧3 recesses which extend radially away from the axis of the hole. | 2013-05-09 |
| 20130116736 | SHEARS WITH TENSIONER AND DYNAMOMETER DEVICE - Shears with tensioner and dynamometer represented by a novel solution in terms of a multi-functional pliers-type tool for adjusting products of the clamp type, in which these pliers are provided with functions of application, tensioning, and cutting/finishing, and in order to obtain better ergonomic conditions for the use of the pliers a novel device for tensioning the metal clamp ( | 2013-05-09 |
| 20130116737 | Methods for Assessing Renal Neuromodulation Treatment and Associated Systems and Methods - The present technology relates to methods for assessing renal neuromodulation treatment and associated systems and methods. In particular, various embodiments of the present technology relate to assessing the efficacy of an ongoing or completed renal neuromodulation procedure and providing feedback (e.g., visual and/or audible indications) to a clinician with the results of all or part of such procedures. | 2013-05-09 |
| 20130116738 | SINGLE CHAMBER LEADLESS INTRA-CARDIAC MEDICAL DEVICE WITH DUAL-CHAMBER FUNCTIONALITY - A leadless intra-cardiac medical device (LIMD) includes a housing configured to be implanted entirely within a single local chamber of the heart. | 2013-05-09 |
| 20130116739 | METHOD AND SYSTEM FOR DETECTING AND ANALYZING HEART MECAHNICS - Method and apparatus for detecting and analyzing heart mechanical activity at a region of interest of a patient's heart are provided. The method comprises acquiring a time sequence of 2-dimensional X-ray images of a region of interest over at least part of a cardiac cycle; detecting coronary vessels in the X-ray images; tracking the coronary vessels through the sequence of images to identify movements of the coronary vessels; and analyzing the movements of the coronary vessels to quantify at least one parameter characterizing heart wall motion in the region of interest. | 2013-05-09 |
| 20130116740 | SINGLE-CHAMBER LEADLESS INTRA-CARDIAC MEDICAL DEVICE WITH DUAL-CHAMBER FUNCTIONALITY AND SHAPED STABILIZATION INTRA-CARDIAC EXTENSION - A leadless intra-cardiac medical device (LIMD) configured to be implanted entirely within a heart of a patient includes a housing configured to be securely attached to an interior wall portion of a chamber of the heart, and a stabilizing intra-cardiac (IC) device extension connected to the housing. The stabilizing IC device extension may include a stabilizer arm, and/or an appendage arm, or an elongated body or a loop member configured to be passively secured within the heart. | 2013-05-09 |
| 20130116741 | DUAL-CHAMBER LEADLESS INTRA-CARDIAC MEDICAL DEVICE WITH INTRA-CARDIAC EXTENSION - A leadless intra-cardiac medical device includes a housing that is configured to be implanted entirely within a single local chamber of the heart. A first electrode is provided on the housing at a first position such that when the housing is implanted in the local chamber, the first electrode engages the local wall tissue at a local activation site within the conduction network of the local chamber. An intra-cardiac extension is coupled to the housing and configured to extend from the local chamber into an adjacent chamber of the heart. A stabilization arm of the intra-cardiac extension engages the adjacent chamber. A second electrode on the intra-cardiac extension engages distal wall tissue at a distal activation site within the conduction network of the adjacent chamber. | 2013-05-09 |
| 20130116743 | METHOD AND APPARATUS FOR THERAPIES OF THE CARDIOVASCULAR AND CARDIORENAL SYSTEM - A system and method for controlling respiration depth or respiration rate is provided. A bipolar pair of a plurality of electrodes is selected in a location for stimulating a phrenic nerve. Electrical stimulation is delivered through a medical electrical lead electrode proximate phrenic nerve tissue. Modulating respiration is elicited in response to electrical stimulation of the phrenic nerve. | 2013-05-09 |
| 20130116744 | VOA generation system and method using a fiber specific analysis - A system and method for generating an estimated volume of activation (VOA) corresponding to settings applied to a stimulation leadwire includes a processor performing the following: determining, for each of a plurality of neural elements, one or more respective parameters characterizing an electrical distribution along the neural element, looking up the one or more parameters for each of the neural elements in a look-up table (LUT), obtaining threshold values for each of the neural elements recorded in the LUT in association with the looked-up parameters, comparing, for each of the neural elements, a value of the leadwire settings to each of the respective threshold value, estimating based on the comparisons which of the neural elements would be activated by the settings, and generating a structure corresponding to a region including the neural elements estimated to be activated. | 2013-05-09 |
| 20130116745 | NEUROSTIMULATOR SYSTEM, APPARATUS, AND METHOD - The invention relates to a method ( | 2013-05-09 |
| 20130116746 | Transpositional Acoustic Frequency Range In EAS Patients - An electric acoustic stimulation (EAS) hearing system includes a signal processor for processing an acoustic signal input to generate: i. an electrical communications signal representative of an upper electrical range of acoustic frequencies, and ii. an acoustic communications signal representative of a lower acoustic range of acoustic frequencies, the acoustic range including: (1) a lower subrange of acoustic frequencies perceivable by the patient with amplification, and (2) an upper subrange of acoustic frequencies not perceivable by the patient, wherein the signal processor uses frequency transposition to include the upper subrange in the lower subrange. An implanted electrical stimulation subsystem receives the electrical communications signal and delivers a corresponding electrical stimulation signal to auditory neural tissue of an implanted patient. An external acoustic stimulation subsystem receives the acoustic communications signal and delivers a corresponding amplified acoustic stimulation signal to the ear canal of the patient. | 2013-05-09 |
| 20130116747 | MODULAR SPEECH PROCESSOR HEADPIECE - A cochlear implant system includes: an electrode array implanted within a cochlea; an internal processor in communication with the electrode array; an implanted antenna which is electrically coupled to the internal processor; and a modular external headpiece which is removably positioned over the implanted antenna, the modular external headpiece including a core containing a sound processor for processing sound and providing a corresponding signal to the implanted antenna; and a modular component configured to releasably engage the core and supply electrical power to the core. A modular speech processor headpiece includes a core comprising a microphone and sound processor for producing a signal representing ambient sound to be transmitted to a cochlear implant, the core further comprising a number of electrical contacts; and a modular component containing a number of electrical contacts corresponding to the electrical contacts of the core; wherein the core is configured to engage with the modular component such that electrical communication is made between the core and the modular component. | 2013-05-09 |
| 20130116748 | CONTROL AND/OR QUANTIFICATION OF TARGET STIMULATION VOLUME OVERLAP AND INTERFACE THEREFOR - A method and system include a processor that outputs a characterization of a correspondence between a volume of estimated tissue activation and a target and/or side effect stimulation volume, and/or that provides controls by which to modify thresholds and/or amounts according to which the volume of estimated activation is to correspond to the target volume. | 2013-05-09 |
| 20130116749 | SYSTEMS AND METHODS FOR STIMULATION-RELATED VOLUME ANALYSIS, CREATION, AND SHARING - A computer implemented system and method facilitates a cycle of generation, sharing, and refinement of volumes related to stimulation of anatomical tissue, such as brain or spinal cord stimulation. Such volumes can include target stimulation volumes, side effect volumes, and volumes of estimated activation. A computer system and method also facilitates analysis of groups of volumes, including analysis of differences and/or commonalities between different groups of volumes. | 2013-05-09 |
| 20130116750 | METHOD FOR SAFEGUARDING IMPLANTED MEDICAL DEVICES IN A DIAGNOSTIC DEVICE EMITTING ELECTROMAGNETIC RADIATION - A method for safeguarding an implanted medical device from the electromagnetic radiation from a diagnostic device is provided. The method includes detecting the implanted medical device by a bidirectional communication with the diagnostic device, determining a device type of the medical device with the diagnostic device, checking whether the device type of the medical device may be operated without errors under the electromagnetic radiation of the diagnostic device and initiating a protective measure if the device type of the medical device cannot be operated without errors under the electromagnetic radiation. | 2013-05-09 |
| 20130116751 | SYSTEM AND METHOD FOR MAPPING ARBITRARY ELECTRIC FIELDS TO PRE-EXISTING LEAD ELECTRODES - A system for a neurostimulator coupled to electrodes, and a method of providing therapy to a patient using the electrodes implanted within the patient. A target multipole relative to the electrodes is defined. The target multipole is emulated by defining an initial electrical current distribution for the electrodes, such that a first set of active electrodes respectively has electrical current values of a first polarity. Each of the electrical current values of the first polarity is compared to a first threshold value, and at least one of the electrodes in the first active electrode set is zeroed-out based on the comparison. The electrical current value of each of the zeroed-out electrode(s) is redistributed to remaining ones of the electrodes to define a new electrical current distribution for the electrodes. Electrical current is conveyed to the electrodes in accordance with the new electrical current distribution, thereby providing the therapy. | 2013-05-09 |
| 20130116752 | SYSTEMS AND METHODS FOR DETECTING FAULTS AND/OR ADJUSTING ELECTRICAL THERAPY BASED ON IMPEDANCE CHANGES - System and methods for detecting impedance changes and for adjusting electrical therapy based on impedance changes are disclosed herein. A method in accordance with a particular embodiment includes applying a therapeutic, paresthesialess electrical signal to a patient via a patient modulation system that includes a signal delivery device in electrical communication with a target neural population of the patient. The method can include monitoring on a periodic basis an impedance of an electrical circuit that includes the signal delivery device. The method can further include detecting a change in the impedance that indicates a fault and providing an indication that the fault exists. | 2013-05-09 |
| 20130116753 | IMPLANTABLE PULSE GENERATOR COMPRISING MRI CURRENT LIMITING WINDINGS IN HEADER STRUCTURE - In one embodiment, a pulse generator for generating electrical stimulation for delivery to a patient, comprises: a hermetically sealed housing containing pulse generating circuitry; a header coupled to the housing for receiving one or more stimulation leads, wherein feedthrough wires are provided to conduct electrical pulses from the pulse generating circuitry to the header; the header comprising a plurality of connectors for electrically connecting to each terminal of the one or more stimulation leads, wherein an inductive winding is disposed around or adjacent to each of the connector structures and is electrically connected between the respective connector structure and a corresponding feedthrough wire to limit MRI induced heating of a respective electrode of the one or more stimulation leads. | 2013-05-09 |
| 20130116754 | MEDICAL DEVICE CONTACT ASSEMBLIES FOR USE WITH IMPLANTABLE LEADS, AND ASSOCIATED SYSTEMS AND METHODS - Medical devices and contact assemblies for electrical connections between medical device components are disclosed herein. A medical device in accordance with a particular embodiment includes a patient implantable element having a receiving cavity and at least one contact assembly positioned in the receiving cavity. The contact assembly can include a housing having an annular shape with an inner surface defining at least in part an opening. The contact assembly can further include a contact disposed at least partially within the opening and having a plurality of leaf spring portions. | 2013-05-09 |
| 20130116755 | METAL COMPLEXES WITH ORGANIC LIGANDS AND USE THEREOF IN OLEDS - The present invention relates, inter alia, to metal complexes having improved solubility, to processes for the preparation of the metal complexes, to devices comprising these metal complexes and to the use of the metal complexes. M(L)n(L′)m formula 1 where the compound contains a moiety M(L)n of the formula (2) W is equal to the formula (3). | 2013-05-09 |
| 20130116756 | UV-A OR UV-B-EMITTING DISCHARGE LAMP - The invention relates to a discharge lamp with a novel garnet-type Pr or Tm doped phosphor with excellent UV-A and UV-B spectral properties. | 2013-05-09 |
| 20130116757 | METHOD AND DEVICE FOR STABILIZING THE CORNEA - A method and device to stabilize the cornea with fewer adverse effects. In particular, a greater stability and shorter treatment time are to be made possible. To this end, the cornea is locally irradiated successively at different sites so that collagen fibers are indirectly or directly crosslinked at the irradiated sites. In this way, the collagen fibers are advantageously crosslinked in a spatially resolved manner. Accordingly, the entire eye need not be irradiated with tissue-damaging UV light, and regions having a weaker structure can be locally stabilized selectively. The sites of the cornea are preferably irradiated so that the collagen fibers are ionized in each instance by photoabsorption of a plurality of photons which each have an energy below an ionizing energy of a given molecule. After a short treatment period, strong covalent bonds are formed directly between the collagen fibers. Crosslinking agents need not be used. | 2013-05-09 |
| 20130116758 | MONITORING THE COOLING OF SUBCUTANEOUS LIPID-RICH CELLS, SUCH AS THE COOLING OF ADIPOSE TISSUE - A system and method of monitoring, controlling and/or detecting events during the removal of heat from subcutaneous lipid-rich tissue is described. In some examples, the system detects an increase in temperature at a treatment device in contact with the skin of a subject, determines that the increase in temperature is related to a treatment event, and performs an action based on the determination. In some examples, the system shuts off the treatment device, alerts an operator, or reduces the cooling in response to a determined treatment event. | 2013-05-09 |
| 20130116759 | COOLING DEVICE HAVING A PLURALITY OF CONTROLLABLE COOLING ELEMENTS TO PROVIDE A PREDETERMINED COOLING PROFILE - A cooling device for removing heat from subcutaneous lipid-rich cells of a subject having skin is provided. The cooling device includes a plurality of cooling elements movable relative to each other to conform to the contour's of the subject's skin. The cooling elements have a plurality of controllable thermoelectric coolers. The cooling elements can be controlled to provide a time-varying cooling profile in a predetermined sequence, can be controlled to provide a spatial cooling profile in a selected pattern, or can be adjusted to maintain constant process parameters, or can be controlled to provide a combination thereof. | 2013-05-09 |
| 20130116760 | COOLING MEDICAL PAD - A medical pad has multiple layers. A first layer is for containing a first thermal-exchange fluid circulatable therethrough, with the medical pad being operable for thermal exchange between the first thermal-exchange fluid and a patient through a first side of the first layer. A second layer of the medical pad is interconnected to a second side of the first layer, opposite to the first side of the first layer. The second layer encloses a second thermal-exchange fluid that may have a freezing point of 0° C. or less. The medical pad is operable for thermal exchange between the second thermal-exchange fluid and the patient. | 2013-05-09 |
| 20130116761 | Rapid Cooling of Body and/or Brain by Irrigating with a Cooling Liquid - Methods and devices are disclosed for providing therapeutic hypothermia using irrigation of the aerodigestive tract with cooled liquids. The disclosed method provides much more rapid therapeutic cooling to lower temperatures than could previously be achieved, thereby improving clinical outcomes. Novel cooling liquids and cooling devices are disclosed for carrying out the method. An external turbulent flow of cooling liquid may also be applied to the exterior of the head to further promote heat exchange. Multiple embodiments of devices are disclosed for performing rapid induction and maintenance of therapeutic hypothermia either in a hospital setting or in the field so that hypothermic treatment can be quickly instituted before significant tissue damage occurs. Methods are also disclosed for targeting brain cooling by irrigating the upper airway/aerodigestive tract, and more generalized cooling by irrigating the esophagus and/or stomach. | 2013-05-09 |
| 20130116762 | ORAL SURGERY RECOVERY MASK - One example embodiment includes an oral surgery recovery mask for cooling an area of a user's face. The oral surgery recovery mask includes a bladder receptacle. The bladder receptacle includes a first layer and a second layer at least partially secured to the first layer. The oral surgery recovery mask also includes a cooling liquid, where the cooling fluid is configured to be inserted into the bladder receptacle. The oral surgery recovery mask also includes a securing device, where the securing device is configured to hold the oral surgery recovery mask in place relative to the user. | 2013-05-09 |
| 20130116763 | MEDICAL DEVICE COMMUNICATION AND CHARGING ASSEMBLIES FOR USE WITH IMPLANTABLE SIGNAL GENERATORS, AND ASSOCIATED SYSTEMS AND METHODS - Communication and charging assemblies for medical devices are disclosed herein. A communication and charging assembly in accordance with a particular embodiment includes a support element, with a communication antenna and a charging coil coupled to the support element. The charging coil can include wire loops having a plurality of wires and the support element can include a mounting surface shaped to match the charging coil and the communication antenna. In one embodiment, the communication and charging assembly are mounted in a header of an implantable signal generator. | 2013-05-09 |
| 20130116764 | IMPLANTABLE MEDICAL DEVICE LEAD INCLUDING INNER COIL REVERSE-WOUND RELATIVE TO SHOCKING COIL - A medical device lead includes a proximal connector configured to couple the lead to a pulse generator and an insulative lead body extending distally from the proximal connector. The lead also includes an inner conductor and one or more cable conductors coupled to the proximal connector at a proximal end and extending through the lead body. The lead further includes one or more defibrillation coil electrodes coupled to a distal end of the one or more cable conductors. The one or more defibrillation coil electrodes are disposed around and electrically isolated from the inner conductor. The one or more defibrillation coil electrodes have a first winding direction and the inner conductor has a second winding direction opposite the first winding direction. | 2013-05-09 |
| 20130116765 | IMPLANTABLE LEAD ADAPTOR WITH MRI FILTER - A system for use with an implantable lead wire includes an implantable electronic apparatus configured to generate an electrical signal. An implantable lead adaptor is operatively disposed between the proximal end of the implantable lead wire and the implantable electronic apparatus. A band stop filter is housed within the implantable lead adaptor and electrically coupled in series with the implantable lead wire and the implantable electronic apparatus. | 2013-05-09 |
| 20130116766 | LEAD ASSEMBLY INCLUDING A POLYMER INTERCONNECT AND METHODS RELATED THERETO - A lead assembly includes a ring component having mechanical coupling features, and at least one polymer component mechanically coupled with the mechanical coupling features of the ring component. Elongate tubing is disposed over the polymer component and is secured with the polymer component. | 2013-05-09 |
| 20130116767 | IMPLANTABLE MEDICAL DEVICE - A device comprising: a lead extending between a proximal end and a distal end, the lead comprising, at its distal end portion, an electrode element configured for fixing in a first body tissue, the lead further comprising: an anchoring element disposed between the proximal and the distal end for anchoring the device to a second tissue; and an elastic element disposed between the anchoring element and the distal end and configured so as to permit the pulling of the distal end away from the anchoring element against the biasing force of the elastic element. | 2013-05-09 |
| 20130116768 | Composite Medical Textile Material and Implantable Devices Made Therefrom - An implantable composite medical device having a longitudinal length a woven textile portion having yarns interlaced in a woven pattern, a knitted textile portion having yarns interlooped in a knitted pattern. The woven and knitted portions are securably attached to one and the other to provide a composite woven and knitted textile surface along the longitudinal length of the device. The woven portion may have a permeability from about 30 to about 500 ml/min/cm | 2013-05-09 |
| 20130116769 | INTRAVASCULAR STENT AND METHOD OF USE - An expandable stent is implanted in a body lumen, such as a coronary artery, peripheral artery, or other body lumen for treating an area of vulnerable plaque. The invention provides for a an intravascular stent having a plurality of cylindrical rings connected by undulating links. The stent has a high degree of flexibility in the longitudinal direction, yet has adequate vessel wall coverage and radial strength sufficient to hold open an artery or other body lumen. A central section is positioned between distal and proximal sections and is aligned with the area of vulnerable plaque to enhance growth of endothelial cells over the fibrous cap of the vulnerable plaque to reinforce the area and reduce the likelihood of rupture. | 2013-05-09 |
| 20130116770 | SYSTEMS AND METHODS FOR SHEATHING AN IMPLANTABLE DEVICE - Systems and methods are disclosed for delivering a stent to a lumen internal to a body of a patient and for sheathing a stent just prior to an insertion procedure. One embodiment comprises a delivery device having a partially sheathed configuration, a fully sheathed delivery configuration, and a deployed configuration. A panchor (combination pusher and anchor) is configured to engage and limit proximal and distal movement of the implantable device. An outer sheath surrounds a distal portion of an inner member and retains the implantable device near the distal end. The outer sheath is slidably moveable relative to the inner member to deploy the implantable device. Proximal movement of a trigger results in movement of the outer sheath to deploy the implantable device. A sheathing mechanism is configured to crimp and fully sheathe the implantable device prior to a deployment procedure. | 2013-05-09 |
| 20130116771 | SAFETY MECHANISM FOR AN IMPLANTABLE DEVICE DEPLOYMENT APPARATUS - Systems and methods are disclosed for delivering a stent to a lumen internal to a body of a patient and for sheathing a stent just prior to an insertion procedure. One embodiment comprises a delivery device having a partially sheathed configuration, a fully sheathed delivery configuration, and a deployed configuration. A panchor (combination pusher and anchor) is configured to engage and limit proximal and distal movement of the implantable device. An outer sheath surrounds a distal portion of an inner member and retains the implantable device near the distal end. The outer sheath is slidably moveable relative to the inner member to deploy the implantable device. Proximal movement of a trigger results in movement of the outer sheath to deploy the implantable device. A sheathing mechanism is configured to crimp and fully sheathe the implantable device prior to a deployment procedure. | 2013-05-09 |
| 20130116772 | IMPLANTABLE DEVICE DEPLOYMENT APPARATUS - Systems and methods are disclosed for delivering a stent to a lumen internal to a body of a patient and for sheathing a stent just prior to an insertion procedure. One embodiment comprises a delivery device having a partially sheathed configuration, a fully sheathed delivery configuration, and a deployed configuration. A panchor (combination pusher and anchor) is configured to engage and limit proximal and distal movement of the implantable device. An outer sheath surrounds a distal portion of an inner member and retains the implantable device near the distal end. The outer sheath is slidably moveable relative to the inner member to deploy the implantable device. Proximal movement of a trigger results in movement of the outer sheath to deploy the implantable device. A sheathing mechanism is configured to crimp and fully sheathe the implantable device prior to a deployment procedure. | 2013-05-09 |
| 20130116773 | DIAMETER REDUCING TIE ARRANGEMENT FOR ENDOLUMINAL PROSTHESIS - An endoluminal prosthesis may include a tubular body of a biocompatible graft material having proximal and distal ends and anterior and posterior sides. The prosthesis may include at least a first and a second fenestration. The first and second fenestrations may be spaced from one another circumferentially around the tubular body. The prosthesis may include at least one first diameter reducing tie positioned circumferentially on the posterior side of the prosthesis and engaging at least a circumferential segment of the posterior side to restrain the engaged segment from expansion. The prosthesis may include at least one second diameter reducing tie positioned circumferentially between the first and second fenestrations on the anterior side of the prosthesis and engaging at least a circumferential segment of the anterior side to restrain the engaged segment from expansion. | 2013-05-09 |
| 20130116774 | Protuberant Aneurysm Bridging Device and Method of Use - A bridging device for supporting occlusive masses within an aneurysm located at a vascular bifurcation. | 2013-05-09 |
| 20130116775 | PROSTHESIS HAVING PIVOTING FENESTRATION - The present disclosure relates to an endoluminal prosthesis, such as a stent graft that includes one or more fenestrations to accommodate endovascular disease, such as an aneurysm in cases where one or more side branches is involved. In one aspect, the prosthesis includes fenestrations that are pivotable to accommodate the dynamic geometry of the aortic branches. In another aspect, the pivotable fenestrations include a first perimeter, a band of flexible material attached and surrounding the first perimeter, and a second perimeter attached to and surrounding the band of flexible material. The first perimeter, band of flexible material, and second perimeter have a geometric shape. In one aspect, the prosthesis includes at least three pivotable fenestrations. | 2013-05-09 |
| 20130116776 | EXTERNAL AORTIC RING AND SPOOL MECHANISM THEREFOR - A method for repairing an aortic valve of a heart of a patient is provided, the method comprising (1) placing around a portion of an aorta of the patient in a vicinity of the aortic valve, an adjustable implant structure comprising an adjusting mechanism coupled to a first portion of a flexible contraction member; and (2) adjusting a dimension of the aortic valve by adjusting a dimension of the implant structure by rotating a rotatable structure of the adjusting mechanism. Other embodiments are also described. | 2013-05-09 |
| 20130116777 | UNITARY QUICK-CONNECT PROSTHETIC HEART VALVEAND DEPLOYMENT SYSTEM AND METHODS - A quick-connect heart valve prosthesis that can be quickly and easily implanted during a surgical procedure is provided. The heart valve includes a substantially non-expandable, non-compressible prosthetic valve and a plastically-expandable coupling stent, thereby enabling attachment to the annulus without sutures. A small number of guide sutures may be provided for aortic valve orientation. The prosthetic valve may be a commercially available valve with a sewing ring with the coupling stent attached thereto. The coupling stent may expand from a conical deployment shape to a conical expanded shape, and may include web-like struts connected between axially-extending posts. A system and method for deployment includes a hollow two-piece handle through which a balloon catheter passes. A valve holder is stored with the heart valve and the handle easily attaches thereto to improve valve preparation steps. | 2013-05-09 |
| 20130116778 | Replacement Heart Valve Leaflet Stitching Method and Device - A replacement heart valve and stitching method for reducing the unexpanded profile of the replacement heart valve are herein provided. The method includes whip stitching a plurality of leaflets together with a first whip stitch pattern a second whip stitch pattern which overlaps the first whip stitch pattern and is wound in an opposite direction. The method further involves securing the valve leaflets to one another via a running stitch. | 2013-05-09 |
| 20130116779 | TRANSCATHETER ATRIO-VENTRICULAR VALVE PROSTHESIS - A transcatheter atria-ventricular valve prosthesis for functional replacement of an atrio-ventricular valve in a connection channel, having a circumferential connection channel wall structure, between atrial and ventricular chambers of a heart, including an inner device to be disposed in the interior of the connection channel, the inner device having a circumferential support structure which is radially expandable and having a valve attached to the circumferential support structure, and an outer device to be disposed on the exterior of the connection channel, wherein the outer device at least partly extends around the inner device at a radial distance to the inner device, wherein the inner and outer devices form a securing mechanism for securing the circumferential connection channel wall structure therebetween. | 2013-05-09 |
| 20130116780 | IMPLANT HAVING MULTIPLE ROTATIONAL ASSEMBLIES - Apparatus is provided, comprising (1) an annuloplasty structure, shaped to define a perimeter, and configured to be disposed at the annulus of the native valve of the patient; (2) a first adjusting mechanism, coupled to the annuloplasty structure, and configured to adjust the perimeter; (3) at least one longitudinal flexible member, having a first end portion, and a second end portion that is configured to be coupled to tissue of the ventricle of the heart of the patient; and (4) at least a second adjusting mechanism, coupled to the annuloplasty structure such that the second adjusting mechanism is slidable around at least part of the perimeter, coupled to the first end portion of the longitudinal flexible member, and configured to adjust a distance between the second adjusting mechanism and the second end portion of the longitudinal flexible member. Other embodiments are also described. | 2013-05-09 |
| 20130116781 | DISCRETE PRE-ASSEMBLED MONOLITHIC AIOL ASSEMBLAGES AND AIOL ASSEMBLIES INCLUDING SAME - Accommodating intraocular lens (AIOL) assemblies including a discrete pre-assembled monolithic AIOL assemblage and a discrete haptics system having a haptics ring and at least two elongated C-shaped haptics for self-anchoring in a human scleral wall at the ciliary sulcus. The AIOL assemblages include an AIOL capsule and an integrally formed base member. The AIOL assemblages also include an annular haptics support surround posterior to an anterior structure on implantation in a human eye of a supine human. AIOL assemblies are assembled in situ by mounting a haptics system onto a previously implanted AIOL assemblage. The haptics system bears against the annular haptics support surround. The anterior structure is freely telescopically received in the haptics ring. | 2013-05-09 |
| 20130116782 | APPARATUS AND METHODS FOR NIPPLE FORMATION VIA COLLAPSIBLE DEVICES - Apparatus and methods for nipple and breast formation are described where devices precondition or expand a target nipple tissue to reduce the pressure exerted by the skin on an eventual implant. Generally, the apparatus comprises a mold having a contact surface which is curved in conformance with a breast upon which the mold is positionable, the contact surface having an adhesive for securement upon the breast, and the mold defining a cavity along the contact surface which conforms to a size of a nipple to be formed upon the breast and where the cavity further comprises the adhesive for securement to the nipple. A breast enlargement device comprises a cup larger than the target breast and further defines an inner surface which adheres to the breast when contacted. | 2013-05-09 |
| 20130116783 | METHOD FOR FORMING BILAYER PATCHES - A method for injection molding thin materials (sub-millimeter) having low green strength could make certain manufacturing processes significantly more efficient yet has heretofore been unavailable. Provided herein is a method that enables injection molding of thin materials by using a mold with contact surfaces having a low surface energy release agent disposed thereon. The low surface energy release agent may be applied as a coating on a conventional mold or the mold itself or just the contact surfaces thereof may be formed of a low surface energy release material. The method finds particular applicability in making special contour patches for medical and cosmetic implants and prosthetics. A preferred approach involves injection molding a thin layer of unvulcanized material on a cold mold, injection molding a thin layer of vulcanized material on a hot mold, transferring the vulcanized layer to the unvulcanized layer on the cold mold, and removing the combined layers. | 2013-05-09 |
| 20130116784 | Breast Implant with Low Coefficient of Friction Between Internal Shells in an Aqueous Fluid Environment - A fluid-filled surgically-implantable prosthetic device encloses one or more non-enclosing fitted shells arranged adjacent to and in a graduated relation to each other. The invention relates specifically to implantable breast prostheses with a low coefficient of friction between two or more interacting elastomeric shells in an aqueous fluid environment, without the addition of a lubricating agent to the fluid. | 2013-05-09 |
| 20130116785 | SILK BASED IMPLANTABLE MEDICAL DEVICES AND METHODS FOR DETERMINING SUITABILITY FOR USE IN HUMANS - 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. | 2013-05-09 |
| 20130116786 | BREAST PROSTHESIS FILLED WITH MICROSPHERES OF THERMOEXPANDED POLYMER - A breast prosthesis constructed from a bag of elastic material or biocompatible mesh having a front face forming a dome and a rear face forming a base with a sealed and seamless interior cavity filled with microspheres of foam polymers or thereto expanded polymers or a combination of both. | 2013-05-09 |
| 20130116787 | ADJUSTABLE GRAFT ATTACHMENT - A graft attachment device includes a platform member, a ratchet mechanism, and a graft connecting element. The ratchet mechanism includes a rack member and a pawl member coupled to the rack member. The rack member has a first end, a second end, and teeth between the first end and the second end. The platform member is coupled to the first end. The pawl member is configured to engage with the teeth of the rack member such that movement of the pawl with respect to the rack member and the platform member is free in a first direction towards the first end of the rack member while being limited in a second direction towards the second end of the rack member. The second direction is opposite the first direction. The graft connecting element is coupled to the pawl member and configured for attachment to a graft. | 2013-05-09 |
| 20130116788 | PARTIAL JOINT RESURFACING IMPLANT, INSTRUMENTATION, AND METHOD - A partial resurfacing implant for use in repairing an articular cartilage defect site that includes a top articulating portion having a top surface that is configured with at least one radius of curvature to approximate the surface contour of the articular cartilage surrounding the defect site. The implant also includes a supporting plate that has a top surface and a bottom surface. The top surface is attached to the top articulating portion by a locking mechanism. The bottom surface of the supporting plate is constructed to facilitate the insertion of the implant into the defect site. Extending from the bottom surface of the supporting plate is at least one implant fixation portion. The at least one implant fixation portion is integrally connected to and is oriented about normal relative to the bottom surface. A method of repairing an articular cartilage defect with the partial joint resurfacing implant is also disclosed. | 2013-05-09 |
| 20130116789 | BIOACTIVE IMPLANT FOR MYOCARDIAL REGENERATION AND VENTRICULAR CHAMBER RESTORATION - Bioactive implant for myocardial regeneration and ventricular chamber support including an elastomeric microporous membrane. The elastomeric microporous membrane being at least one non-degradable polymer and at least one partially degradable polymer. The non-degradable polymer is selected from polyethylacrylate and polyethylacrylate copolymerized with a hydroxyethylacrylate comonomer. The partially degradable polymer is selected from caprolactone 2-(methacryloyloxy)ethyl ester and caprolactone 2-(methacryloyloxy)ethyl ester copolymerized with ethylacrylate. The elastomeric microporous membrane further includes a nanofiber hydrogel, and cells. The bioactive implant, having one or two helical loops, contributes to the restauration of the heart conical shape. Cardiac wrapping by ventricular support bioprostheses of the present invention, having reinforcement bands spatially distributed as helicoids, recovers the sequential contraction of the myocardium resulting in the successive shortening and lengthening of the ventricles, therefore improving the ejection (systolic function) and suction of blood (diastolic function). | 2013-05-09 |
| 20130116790 | Intervertebral Spinal Implant - An intervertebral implant for implantation in a treated area of an intervertebral space between vertebral bodies of a spine is provided. The upper surface and the lower surface of the implant each have a contact area capable of engaging with anatomy in the treated area, and the upper and lower surfaces define a through-hole having an inner surface extending through the spacer body. A first and second sidewalls extend from a front end and a back end, wherein the first and second sidewalls are configured with engagement portions positioned in close proximity to the front end and the back end. The front end and the back end are configured with a threaded hole for receiving an instrument for inserting the intervertebral implant into the intervertebral disc space. | 2013-05-09 |
| 20130116791 | Expandable intervertebral spacer implant - Expandable intervertebral spacer implants are illustrated for insertion into an intervertebral space between a superior vertebral body and an inferior vertebral body. The implant is formed as a first and second member having a variable distance therebetween, each member having a first end and a second end with a length therebetween, a proximal side and a distal side with a width therebetween, and a pair of internally guided legs which are rotatable about one or more common axes and are positioned to successively interlock with a plurality of detents formed within each said first and second members to facilitate maintenance of a specific distance therebetween. | 2013-05-09 |
| 20130116792 | COMPOSITE IMPLANT - A composite interbody vertebral implant for facilitating fusion of adjacent vertebrae. The implant includes a first endplate of a porous metal material and a second endplate of a porous metal material which are configured to allow bone in-growth. The implant also includes a polymeric body positioned between and bonded to the first and second endplates such that polymeric material of the polymeric body is impregnated into pores of the first and second endplates to bond the components together. The implant may include a cavity extending through the composite implant configured to receive bone growth material to facilitate fusion between a first vertebra and a second vertebra. | 2013-05-09 |
| 20130116793 | SURGICAL IMPLANT - The present invention is directed to a surgical implant for the fusion of two adjacent vertebrae with an upper plane for contacting an upper vertebral body and a lower plane for contacting a lower vertebral body and a tubular structure, wherein the tubular structure is formed by a plurality of tubes running from the upper plane to the lower plane and in substantially horizontal direction throughout one side of the surgical implant straight to the opposite side of the surgical implant. This tubular structure has the advantage that the formation and ingrowth of new bone is promoted and advantaged and that the degree of formation and ingrowth of new bone is detectable by X-ray measurements. | 2013-05-09 |
| 20130116794 | SHOULDER IMPLANT - Apparatus and method for a shoulder implant, for example, for the glenohumeral joint. Optionally, The implant is expandable and deflatable during implantation. Optionally the implant is sized for the gelnoid fossa. In an exemplary embodiment of the invention, the selection and/or implantation of the implant include adapting the implant by size and function to a particular patient's need. | 2013-05-09 |
| 20130116795 | FEMORAL TRIAL COMPONENT - An orthopaedic surgical instrument including a femoral trial component configured to be coupled to a surgically-prepared distal end of a patient's femur. The femoral trial component has a fixation side configured to engage a posterior aspect of the surgically-prepared distal femur. | 2013-05-09 |
| 20130116796 | DISTAL RADIOULNAR JOINT DEVICE - A system and method of implanting a distal wrist implant relative to a host bone is presented. A distal radial component having a body including a first connection portion couplable to a stem is coupled to a second prosthetic coupled to a medial surface of the body. The second prosthetic replaces at least a portion of the sigmoid notch. | 2013-05-09 |
| 20130116797 | SURGICAL INSTRUMENTATION ASSEMBLY FOR POSITIONING AN ANKLE PROSTHESIS - In order to position an ankle prosthesis including a tibial implant and a talus implant provided with a talo-calcaneal anchoring keel, the invention proposes a surgical instrumentation assembly including: a tibial phantom ( | 2013-05-09 |
| 20130116798 | BONE ADHESIVE AND A METHOD OF DELIVERY - An adhesive precursor and method of delivering an adhesive precursor for fixing bone fragments together. | 2013-05-09 |
| 20130116799 | REINFORCED TISSUE GRAFT - A biocompatible tissue graft includes a first layer of a bioremodelable collageneous material, a second layer of biocompatible synthetic or natural remodelable or substantially remodelable material attached to the first layer; and at least one fiber that is stitched in a reinforcing pattern in the first layer and/or second layer to mitigate tearing and/or improve fixation retention of the graft, and substantially maintain the improved properties while one or more of the layers is remodeling. | 2013-05-09 |
| 20130116800 | CONTROL APPARATUS AND COMMUNICATIONS CONTROL METHOD - A control apparatus is disclosed, including a first processor which can be connected to a network; and a second processor which includes a user interface, which is communicatively connected to the first processor, and which performs equipment control based on information input via the user interface and information obtained by the first processor from the network, wherein the first processor includes a communications control unit which conducts a protocol control and/or cryptographic process in communications via the network. | 2013-05-09 |
