| 06th week of 2015 patent applcation highlights part 56 |
| Patent application number | Title | Published |
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| 20150038995 | DEVICES, SYSTEMS, AND METHODS FOR WOUND CLOSURE - A wound closure device includes outer and inner members. The inner member is configured for receipt of a suture passer and is pivotably coupled to the outer member. The inner member is pivotable relative to the outer member between a first position, wherein the inner member is coaxially disposed relative to the outer member, a second position, wherein the distal end of the inner member extends outwardly from the outer member in a first direction and the proximal end of the inner member extends outwardly from the outer member in a second, opposite direction, and a third position, wherein the distal end of the inner member extends outwardly from the outer member in the second direction and the proximal end of the inner member extends outwardly from the outer member in the first direction. | 2015-02-05 |
| 20150038996 | DEVICES, SYSTEMS, AND METHODS FOR PROVIDING SURGICAL ACCESS AND FACILITATING CLOSURE OF SURGICAL ACCESS OPENINGS - A method of surgery includes positioning a cannula within an opening in tissue and inserting a guide member into the cannula. The cannula includes an elongated portion having a base and an elongated tubular member extending distally from the base. The elongated tubular member includes an annular wall defining a longitudinal passageway. At least one slot extends through the annular wall and is disposed in communication with the longitudinal passageway. The guide member includes a guide housing and an elongated guide shaft. The guide member defines at least one lumen extending therethrough. The method further includes releasably engaging the guide housing with the base. Upon engagement of the guide housing with the base, the at least one lumen is aligned with the at least one slot to define a guide passageway through the guide member and cannula. | 2015-02-05 |
| 20150038997 | DEVICES, SYSTEMS, AND METHODS FOR PROVIDING SURGICAL ACCESS AND FACILITATING CLOSURE OF SURGICAL ACCESS OPENINGS - A guide member configured for guiding a suture passer through a cannula and tissue surrounding the cannula to facilitate closure of an opening in tissue. The guide member includes a guide housing and an elongated guide shaft. The guide housing is configured for releasably engaging the guide member with the cannula and defines an entry aperture. The elongated guide shaft extends distally from the guide housing and defines an annular exterior surface. An exit aperture is defined through the annular exterior surface. The guide member defines a lumen extending from the entry aperture, through the guide housing and the elongated guide shaft, to the exit aperture. The entry aperture, lumen, and exit aperture cooperating to define a passageway extending through the guide member. | 2015-02-05 |
| 20150038998 | TENDON ANCHOR AND METHOD OF USING SAME - A tendon anchor, a housing, a protuberance located substantially on the housing, a cut-out area located substantially on the housing and located substantially across from the protuberance, and a plurality of elongated tendon gripping projections located substantially adjacent to the protuberance and the cut-out area for substantially retaining the tendon within the tendon anchor. | 2015-02-05 |
| 20150038999 | METHOD AND APPARATUS FOR COUPLING LEFT VENTRICLE OF THE HEART TO THE ANTERIOR INTERVENTRICULAR VEIN TO STIMULATE COLLATERAL DEVELOPMENT IN ISCHEMIC REGIONS - A method for stimulation of collateral development in ischemic cardiac regions comprises the fluid coupling of the left ventricle of the heart to the anterior interventricular vein to stimulate collateral development in ischemic regions. The fluid coupling of the left ventricle of the heart to the anterior interventricular vein includes a control of the diastolic/systolic pressure in the venous system to be within about | 2015-02-05 |
| 20150039000 | SYSTEM FOR TISSUE FIXATION TO BONE - Methods and systems are provided for fixating connective tissue to bone. 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 of an animal; and a bone engaging member extending from the carrier member and configured to attach to a bone of the animal. In some aspects, when the attachment members are engaged with the connective tissue and the bone engaging member is attached to the bone, the connective tissue and the bone are limited in being pulled apart from one another during physiological use of the connective tissue. | 2015-02-05 |
| 20150039001 | 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. | 2015-02-05 |
| 20150039002 | ANGIOPLASTY BALLOON - Described here are angioplasty balloon devices for generating shock waves to break up calcified plaques along a length of a vessel and methods of making such devices. Generally, the devices may be used in angioplasty and/or valvuloplasty procedures, but may alternatively be used in other applications. In some variations, the device may include an elongate member, a plurality of electrode assemblies, and at least one tubular sleeve interposed between adjacent or neighboring electrode assemblies that form a continuous outer profile between the electrode assemblies. These devices may have a smooth, continuous outer profile without substantial profile transitions and/or may have stiffening sections between electrode assemblies. | 2015-02-05 |
| 20150039003 | Nose Comforter And Cleaning Device - A disposable hygienic nostril cleansing tool is described that consists of a dual-purpose head (cotton swab and scraper tip), flexible shaft, and cotton debris cleaner in the tool body. | 2015-02-05 |
| 20150039004 | Vascular Re-Entry Device - An ultrasonic device having a tri-axial configuration including an ultrasound transmission member, a dilator, and a sheath is disclosed. The ultrasound device may be used in a procedure to treat an occluded blood vessel. The ultrasound transmission member can transmit ultrasonic energy from an ultrasonic transducer to a distal end. The dilator facilitates entry of the ultrasonic transmission member into the subintimal space of a blood vessel. The sheath may articulate to aid in the process of re-entering the central lumen of the blood vessel. | 2015-02-05 |
| 20150039005 | System and Method for Minimally Invasive Tissue Treatment - Delivering ultrasonic energy to a target musculoskeletal tissue site includes connecting a delivery device to a vacuum source, a fluid source, and a power signal source. The delivery device has a housing portion maintaining an ultrasound transducer and a tip portion having a sleeve and a cannula. The cannula is coupled to the ultrasound transducer and received in the sleeve to define a covered portion and an exposed portion. Ultrasonic energy is generated by sending a power signal from the power signal source to the ultrasound transducer. The ultrasonic energy is transmitted from the ultrasound transducer to the cannula, such that the exposed portion of the cannula delivers ultrasonic energy at a frequency that is pre-selected to debride musculoskeletal tissue upon percutaneous insertion of the tip portion. | 2015-02-05 |
| 20150039006 | SINGLE USE LANCET ASSEMBLY - A single use lancet device having a housing, with an open interior and an access opening defined therein, a lancet, with a body and a piercing tip, and disposed in the open interior of the housing so as to move between a cocked orientation and a piercing orientation, a driving assembly structured to move the lancet into the piercing orientation, and a restrictor assembly having a shoulder element and a restrictor panel operatively associated with the lancet and the housing and structured to pass over the restrictor panel upon the lancet moving from its cocked orientation to its piercing orientation, and to abut the restrictor panel upon attempted movement of the lancet back into its cocked orientation after movement into the piercing orientation, thereby preventing the lancet from moving back into the cocked orientation and preventing re-use of a contaminated piercing tip. | 2015-02-05 |
| 20150039007 | Methods and Structures for Assembling Lancet Housing Assemblies for Handheld Medical Diagnostic Devices - A method of assembling a lancet housing assembly comprising multiple lancets for use in a portable handheld medical diagnostic device for sampling bodily fluids from a skin site of a patient is disclosed. The method includes forming a plurality of lancet structures in a lancet sheet. The lancet sheet has a removable ledge for releasing the lancet structures. The removable ledge of the lancet sheet is flexed for releasing the lancet structures from the removable ledge. | 2015-02-05 |
| 20150039008 | SURGICAL INSTRUMENT - Provided is a suture instrument capable of shortening operation time required to ligate a wound, and cauterizing the wound. Provided is a surgical needle including a shape memory alloy which has been shape memory-processed to return, at a temperature equal to or higher than its transformation point, to its original shape selected from a group consisting of a ring shape, a spiral shape, a coil shape and a clinch shape. Use of the surgical needle of the present invention makes it unnecessary to employ a threaded suture needle, shortens the operation time required to ligate an incised part or a wound in an organ such as the digestive tract in the body or the skin or the like, and allows cauterization of the wound. | 2015-02-05 |
| 20150039009 | PUNCTURE DEVICE - To provide a puncture device which prevents components constituting a puncture device from being damaged by buckling (bending) etc., secures safety, and can be handled by a weak user easily. A puncture device | 2015-02-05 |
| 20150039010 | DISSECTION TIP AND INTRODUCER FOR SURGICAL INSTRUMENT - The present disclosure describes a surgical fastener applying apparatus that includes an elongate body portion having proximal and distal ends, an end effector including a first movably coupled to a second jaw that is positioned at the distal end of the elongate body portion, and an introducer member. The introducer member has proximal and distal portions, and is configured and dimensioned for releasable connection with the end effector. The introducer member is at least partially formed from a flexible material, and is configured and dimensioned to separate target tissue from collateral tissue prior to positioning of the target tissue between the first and second jaws of the end effector. | 2015-02-05 |
| 20150039011 | GASTRIC SPACE OCCUPIER SYSTEMS AND METHODS OF USE - Systems for controlling obesity utilize a number of space occupiers positioned in the stomach to reduce the effective volume of the stomach. Such arrangements provides sufficient stomach volume consumption to induce weight loss, but enable use of space occupiers that are proportioned to minimize the threat of obstruction even if they should migrate into the intestine. In general, numerous small volume space occupiers are placed in the stomach such that the total volume equals or exceeds the single volume of prior art single unit space occupiers. However, each individual space occupier is proportioned so that it will pass without obstruction if it moves into the intestine. | 2015-02-05 |
| 20150039012 | SYSTEMS AND METHODS FOR TREATING A VESSEL USING FOCUSED FORCE - A device for introduction into a body vessel includes a main elongated element, a balloon positioned at the main elongated element distal end, a distal connecting element positioned at the distal end of the balloon to receive a guidewire during use, and a longitudinally movable sheath positioned external to the main elongated element, a position of the sheath distal end with respect to the balloon defining an exposed portion of the balloon that expands when fluid is delivered to the balloon through the inflation lumen. | 2015-02-05 |
| 20150039013 | Nasolacrimal obstruction treatment device and method - A device and method for performing probing and intubation of the nasolacrimal system includes a tubular probe through which a tracer fluid is injected and collected in the nasal cavity to verify that the tip of the probe has passed through an obstruction and reached the nasal cavity. A sleeve fitted over the probe has distal segment that is inflated in order to retain the sleeve in the nasolacrimal system once the tubular probe has been withdrawn. Removal of blood and other obstructions encountered during the probing or intubation process is accomplished by connecting the proximal end of the probe to a suction device. | 2015-02-05 |
| 20150039014 | Methods of Locating and Treating Tissue in a Wall Defining a Bodily Passage - Devices, kits, and methods of treatment are described. More particularly, methods of treating tissue of a passage wall defining a bodily passage, such as a sinus cavity, airway, or sinus passage are described. An exemplary method utilizes an elongate member having an elongate member proximal end, elongate member distal end, and an elongate member body that defines a curve. | 2015-02-05 |
| 20150039015 | ANEURYSM DEVICES WITH ADDITIONAL ANCHORING MECHANISMS AND ASSOCIATED SYSTEMS AND METHODS - The present technology relates to aneurysm devices with additional anchoring mechanisms, and associated systems and methods. In some embodiments, the aneurysm devices are endovascularly deliverable to a site proximate an aneurysm near a parent artery with bifurcating branches. The aneurysm devices can include a closure structure ( | 2015-02-05 |
| 20150039016 | DEVICE AND METHOD FOR DEFLECTING EMBOLI IN AN AORTA - The invention features an intra-vascular device (10) which may include a filter (30), a filter insert (36), and a supporting structure (40) to hold a filtering element and may serve to filter or deflect emboli or other large objects from entering protected secondary vessels. The device may be capable of collapse along its longitudinal axis (80) for ease of delivery to the treatment site. The device may further be compatible with common delivery methods (e.g., TAVI procedures). Upon deployment, the device may be positioned in a middle area of a blood vessel (e.g., an aortic arch) near but not in contact with one or more second blood vessels (e.g., the branch arteries of the aorta). The supporting structure may be capable of pressing against the medial wall of a blood vessel (e.g., the aorta) and provide lift to the device so that a middle portion of the device is above a lateral plane of the device. | 2015-02-05 |
| 20150039017 | METHODS AND DEVICES FOR ENDOVASCULAR EMBOLIZATION - The present disclosure describes an occlusion device and methods of delivering the occlusion device. The occlusion device can include an expandable structure configured to move between an unexpanded configuration and an expanded configuration. The expandable structure can be configured to have an expansion ratio of at least about 5:1. Further, the occlusion device can be configured to prevent substantially all fluid from flowing past the occlusion device when the occlusion device is in the expanded configuration in the vessel. | 2015-02-05 |
| 20150039018 | METHODS AND DEVICES FOR ENDOVASCULAR EMBOLIZATION - The present disclosure describes an occlusion device and methods of delivering the occlusion device. The occlusion device can include an expandable structure configured to move between an unexpanded configuration and an expanded configuration. The expandable structure can be configured to have an expansion ratio of at least about 5:1. Further, the occlusion device can be configured to prevent substantially all fluid from flowing past the occlusion device when the occlusion device is in the expanded configuration in the vessel. | 2015-02-05 |
| 20150039019 | METHODS AND DEVICES FOR ENDOVASCULAR EMBOLIZATION - The present disclosure describes an occlusion device and methods of delivering the occlusion device. The occlusion device can include an expandable structure configured to move between an unexpanded configuration and an expanded configuration. The expandable structure can be configured to have an expansion ratio of at least about 5:1. Further, the occlusion device can be configured to prevent substantially all fluid from flowing past the occlusion device when the occlusion device is in the expanded configuration in the vessel. | 2015-02-05 |
| 20150039020 | METHODS AND DEVICES FOR ENDOVASCULAR EMBOLIZATION - The present disclosure describes an occlusion device and methods of delivering the occlusion device. The occlusion device can include an expandable structure configured to move between an unexpanded configuration and an expanded configuration. The expandable structure can be configured to have an expansion ratio of at least about 5:1. Further, the occlusion device can be configured to prevent substantially all fluid from flowing past the occlusion device when the occlusion device is in the expanded configuration in the vessel. | 2015-02-05 |
| 20150039021 | IMPLANT RETRIEVAL SYSTEM - Disclosed is an adjustable occlusion device for use in a body lumen such as the left atrial appendage. The occlusion device is removably carried by a deployment catheter. The device may be enlarged or reduced to facilitate optimal placement or removal. Methods are also disclosed. | 2015-02-05 |
| 20150039022 | 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. | 2015-02-05 |
| 20150039023 | CLOSURE SYSTEM FOR ATRIAL WALL - A closure system, assembly and attended method for closing and opening in the tissue of the patient includes first and second closure members each including a biased construction operative for disposition of the closure members into an out of retracted and expanded orientations. A connector is disposed in interconnecting relation with the closure members and structured to establish at least a partial spacing there between. The biased construction and the interconnection of the closure members facilitate con current disposition of the closure members with one another into and through an introductory instrument as well as independent and successive disposition of the first and second closure members into a closing relation to the tissue opening upon exiting the introductory instrument. | 2015-02-05 |
| 20150039024 | SURGICAL TACK AND TACK DRIVE APPARATUS - A fastener is provided for attaching body tissue to body tissue or another material to body tissue. The fastener includes a head portion, a body portion, and an anchoring element. The anchoring element is on the distal end of the fastener, and has one or more barbs or similar anchoring devices that are configured to prevent removal of the fastener once it is attached to the body tissue. The head is located on the proximal end of the fastener, and anchors the body tissue or other material when the fastener is attached to the body tissue. The disclosure also provides a driver apparatus for inserting the fasteners. The applicator device includes an indexer for sequentially indexing one or more fasteners, and a driver for applying an insertion force to a fastener that is sufficient to insert the fastener and attach it to body tissue. The disclosure also provides a method of using the fastener and applicator device. | 2015-02-05 |
| 20150039025 | DEVICES, SYSTEMS, AND METHODS FOR WOUND CLOSURE - A wound closure device includes a shaft, a sleeve, a suture, and a cartridge. The sleeve is disposed about the shaft and defines first and second sleeve arms movable between a retracted position, wherein the sleeve arms extend along the shaft, and a deployed position, wherein the sleeve arms extend outwardly from the shaft. The cartridge includes a base and first and second cartridge arms. The base is configured for releasable coupling with the shaft and defining a pocket configured to retain an intermediate portion of the suture. The first and second cartridge arms are configured for positioning adjacent the respective first and second sleeve arms and are configured to move in conjunction with the respective first and second sleeve arms between the retracted and deployed positions. The first and second cartridge arms are configured to retain first and second ends of the suture, respectively. | 2015-02-05 |
| 20150039026 | ADJUSTABLE GRAFT FIXATION DEVICE - Systems and methods for securing a soft tissue graft to bone are provided herein. In one embodiment, a surgical implant can include an elongate body having a longitudinal axis extending therealong and having first and second through-holes that are offset to a first side of the longitudinal axis and a third through-hole that is offset to a second side of the longitudinal axis and that is positioned between the first and second through-holes. The implant can also include a suture length extending through the first, second, and third through-holes such that a self-locking knot is formed on a first side of the body and a plurality of suture loops are formed on a second side of the body opposite the first side. | 2015-02-05 |
| 20150039027 | Tissue Fixation Device - A tissue fixation device includes an elongated body extending between a proximal portion and a distal portion including a plurality of barbed loops. The elongated body, proximal portion, and distal portion are provided in a variety of configurations depending upon the performance requirements desired of the tissue fixation device for the envisaged application of use. | 2015-02-05 |
| 20150039028 | SUTURE ANCHOR APPARATUS - In various examples, a suture anchor includes a sheath including a lumen. A frame member is disposed at least partially within the sheath. The frame member includes at least two suture loops extending from the sheath. The suture loops are configured to receive a suture, wherein tightening of the suture causes compression of the frame member to constrict the lumen of the sheath. | 2015-02-05 |
| 20150039029 | IMPLANT DEVICE AND SYSTEM FOR STABILIZED FIXATION OF BONE AND SOFT TISSUE - A system for syndesmosis repair includes a flat band secured to bone by pulling a metal button through both the tibial and fibula bones, which button is then toggled into position to create tension, along the band, across the two bone segments to be fixated. Once the button is secure against the bone, flat suture tails against the lock at the initial insertion site serves to tension the band and bone segments in place. The system band offers syndesmosis repair with a knotless closure. The system is designed to provide this stabilized fixation for bone fractures, osteotomies, and arthrodesis, plus soft tissue to bone attachment, if desired. It is designed to apply a restorative fixation force across the tissue segments to stabilize them. The band's rigidity and compliant nature provides consistent and rigid fixation during the healing phase. | 2015-02-05 |
| 20150039030 | TRANSOSTEAL ANCHORING METHODS FOR TISSUE REPAIR - Described herein are methods and apparatuses for use in repair of a patient's tissue by connecting the tissue to the bone using a transosteal tunnel and anchor configured to pass through the transosteal tunnel. In particular, described herein are methods of repairing an anterior cruciate ligament (ACL) and torn meniscal root. These anchoring apparatuses and method of using them are particularly well suited for use with the low-profile suture passers described herein, since these suture passers may allow access to previously inaccessible regions of the knee (or other body regions). | 2015-02-05 |
| 20150039031 | SURGICAL FASTENING - A surgical device includes a first fastener having a planar profile, a second fastener having a concave surface, and a suture that can be manipulated to change a distance between the first and second fasteners. The second fastener has a curvature that substantially matches the curvature of a top surface of a clavicle bone in a direction perpendicular to a long axis of the clavicle bone. A method of treating an acromioclavicular joint injury includes forming axially aligned passages through a patient's clavicle and coracoid process, passing a fastener having a concave surface through the passages, positioning the concave surface of the fastener against a top surface of the patient's clavicle with a long axis of the fastener extending perpendicular to a long axis of the clavicle, positioning a fastener having a planar profile below the patient's coracoid process, and adjusting a suture that couples the fasteners. | 2015-02-05 |
| 20150039032 | Lateral Spinous Process Spacer - Interspinous process implants are disclosed. Also disclosed are systems and kits including such implants, methods of inserting such implants, and methods of alleviating pain or discomfort associated with the spinal column. | 2015-02-05 |
| 20150039033 | IMPLANT FOR BONES OR VERTEBRAE WITH SELF-CONSTRAINED FLEXIBILITY - As implant for the stabilization of bones or vertebrae is provided, the implant being a solid body including a longitudinal axis that defines a longitudinal direction and including a flexible section that has a surface and has a length in the longitudinal direction, the flexible section including at least one cavity located near the surface and having a width in the longitudinal direction that is smaller than the length of the flexible section, the at least one cavity being connected to the surface through at least one slit, and a width of the slit in the longitudinal direction being smaller than the width of the cavity. | 2015-02-05 |
| 20150039034 | SKELETAL BONE FIXATION MECHANISM - A skeletal fixation apparatus may include two or more bodies that are attached to two or more screws that have been inserted into vertebral bodies associated with a patient. The apparatus may also include two or more cylindrical members that are attached to the bodies to control the movement or alignment of the bodies when the skeletal fixation apparatus is being installed in the patient. The apparatus may further include a rod that includes a first curvature and a second curvature. The first curvature may be different than the second curvature and may be based on a medical diagnosis associated with stabilizing the vertebral bodies. The second curvature may enable the bodies to be immovably fastened to the rod in a manner that precludes the cylindrical members from contacting each other or causing a false torque condition to exist when the skeletal fixation apparatus is installed in the patient. | 2015-02-05 |
| 20150039035 | MEDICAL INSTRUMENT FOR HOLDING AND HANDLING A SURGICAL SECURING ELEMENT, AND VERTEBRAL COLUMN STABILIZATION SYSTEM - A medical instrument for holding and handling a surgical securing element has a proximal and a distal end. The surgical securing element includes a securing part and a holding part, and is assembled such that in an assembled disposition, the holding part for a connection element is movable in relation to the securing part. The instrument defines a longitudinal axis and includes a pulling part and, movable in relation to the latter in the direction of the longitudinal axis, a pushing part. The proximal end is temporarily couplable to the securing element in the assembled disposition. The instrument further includes an uncoupling device for actively transferring the instrument from a coupled position, in which the pulling part and the holding part are coupled, to an uncoupled position, in which the pulling part and the holding part are separable from one another. | 2015-02-05 |
| 20150039036 | LOW PROFILE SPINAL TETHERING DEVICES - Methods and devices for treating spinal deformities are provided. In one exemplary embodiment, a low-profile spinal anchoring device is provided for receiving a spinal fixation element, such as a tether, therethrough. The device generally includes a staple body that is adapted to seat a spinal fixation element, a fastening element for fixing the staple body to bone, and a locking assembly for coupling a spinal fixation element to the staple body. In one embodiment, the locking assembly includes a washer that is adapted to couple to the staple body such that the spinal fixation is disposed therebetween, and a locking nut that is adapted to engage the staple body to mate the washer to the staple body. | 2015-02-05 |
| 20150039037 | SYSTEMS FOR AND METHODS OF PREPARING A SACROILIAC JOINT FOR FUSION - A surgical preparation tool for preparing a sacroiliac joint for a surgical procedure comprising a trial tool assembly and a cutting tool configured to releasably and slidably couple with the trial tool assembly, wherein the trial tool assembly is configured to guide the cutting tool during distal-proximal translation such that as the cutting tool distally advances relative to an implant trial of the trial tool assembly, at least a portion of a cutting element of the cutting tool extends generally over and perpendicularly outward from a first top surface of a body of the implant trial. | 2015-02-05 |
| 20150039038 | Orthopedic Screw Fastener System Including Locking and Non-Locking Screws - An orthopedic screw fastener system which includes at least two screws and at least one bone plate. At least one screw is a locking screw comprising a screw head and a screw shank, the screw head being provided with a thread. At least one other screw is a non-locking screw comprising a non-threaded (i.e., smooth) screw head and a screw shank. The at least one bone plate has a thickness and it has at least two through-bores which are able to receive screws. The plate has two or more through-openings, each formed by at least two through-bores, each through-bore being defined by a midpoint and by a radius, and the through-bores are offset relative to each other and intersect each other in such a way that intersection lines and/or intersection surfaces extend into the depth of the through-opening. | 2015-02-05 |
| 20150039039 | Compact Controller Device for Defibrillator - A defibrillator includes: a housing; a discharge module disposed on a first portion of a printed circuit board and positioned within the housing; an energy storage module disposed on a second portion of the printed circuit board; and a controller module disposed on a third portion of the printed circuit board. The energy storage module is operatively connected to the discharge module by a first flexible member. The controller module is operatively connected to the energy storage module by a second flexible member. The first flexible member is folded such that the first portion of the printed circuit board is positioned substantially parallel to the second portion of the printed circuit board and the second flexible member is folded such that the third portion of the printed circuit board is positioned substantially perpendicular to the first and second portions of the printed circuit board. | 2015-02-05 |
| 20150039040 | WEARABLE DEFIBRILLATOR SYSTEM COMMUNICATING VIA MOBILE COMMUNICATION DEVICE - A wearable defibrillation system can establish a local comlink with a mobile communication device, such as a smartphone, tablet-type computer and the like. The mobile communication device can in turn establish a remote comlink with other devices in a network such as the internet. Accordingly, communication tasks relating to the wearable defibrillation system can be performed via the local and the remote comlinks, with or without the participation of the patient, who is wearing the system. The wearer can thus use the familiar interface of a mobile communication device for interacting with his defibrillator system. Moreover, he can do so while keeping on his regular clothes, which could conceal completely the wearable defibrillator system. The patient can thus preserve his dignity and privacy. | 2015-02-05 |
| 20150039041 | MODULAR ANTITACHYARRHYTHMIA THERAPY SYSTEM - This document discusses, among other things, a modular antitachyarrhythmia therapy system. In an example, a modular antitachyarrhythmia system includes at least two separate modules that coordinate delivery an antitachyarrhythmia therapy, such as defibrillation therapy. In another example, a modular antitachyarrhythmia therapy system includes a sensing module, an analysis module, and a therapy module. | 2015-02-05 |
| 20150039042 | Indicators on a Wearable Medical Therapy Device - A medical therapy device comprises: a housing; a controller positioned within the housing for monitoring a condition of a patient based on a signal received from at least one sensor associated with the patient and initiating a treatment based on the condition of the patient; and at least one indication mechanism provided on the housing and configured to provide an indication to the patient of at least one condition of at least one of the medical therapy device, the at least one sensor, and the patient. The at least one indication mechanism is visible without manipulation of the housing of the medical therapy device. | 2015-02-05 |
| 20150039043 | SUBCUTANEOUS CARDIAC SENSING AND STIMULATION SYSTEM - Cardiac systems and methods using ECG and blood information for arrhythmia detection and discrimination. Detection circuitry is configured to produce an ECG. An implantable blood sensor configured to produce a blood sensor signal is coupled to a processor. The processor is coupled to the detection and energy delivery circuitry, and used to evaluate and treat cardiac rhythms using both the cardiac electrophysiologic and blood sensor signals. The blood sensor is configured for subcutaneous non-intrathoracic placement and provided in or on the housing, on a lead coupled to the housing, and/or separate to the housing and coupled to the processor via hardwire or wireless link. The blood sensor may be configured for optical sensing, using a blood oxygen saturation sensor or pulse oximeter. A cardiac rhythm may be evaluated using the electrocardiogram signal and the blood sensor signal, and tachyarrhythmias may be treated after confirmation using the blood sense signal. | 2015-02-05 |
| 20150039044 | SYSTEMS AND METHODS FOR RANKING AND SELECTION OF PACING VECTORS - Approaches to rank potential left ventricular (LV) pacing vectors are described. Early elimination tests are performed to determine the viability of LV cathode electrodes. Some LV cathodes are eliminated from further testing based on the early elimination tests. LV cathodes identified as viable cathodes are tested further. Viable LV cathode electrodes are tested for hemodynamic efficacy. Cardiac capture and phrenic nerve activation thresholds are then measured for potential LV pacing vectors comprising a viable LV cathode electrode and an anode electrode. The potential LV pacing vectors are ranked based on one or more of the hemodynamic efficacy of the LV cathodes, the cardiac capture thresholds, and the phrenic nerve activation thresholds. | 2015-02-05 |
| 20150039045 | METHOD AND SYSTEM FOR APPLYING STIMULATION IN TREATING SLEEP DISORDERED BREATHING - A stimulation protocol determination system includes an input module and a selector module. The input module is provided to receive an indication of an upper airway flow limitation via sensed respiratory effort information. The selection module is provided to automatically select, based on the indicated upper airway flow limitation, a stimulation protocol. | 2015-02-05 |
| 20150039046 | BILATERAL FEEDBACK - Apparatus comprising (1) a breathing sensor, configured to detect a breathing-related factor of a subject; (2) at least a first electrode configured to be placed in a vicinity of a respective first hypoglossal nerve, and to be driven, in response to the detected breathing-related factor, to apply a first electrical current to the first hypoglossal nerve; (3) at least a second electrode configured to be placed in a vicinity of a respective second hypoglossal nerve, and to be driven, in response to the detected breathing-related factor, to apply a second electrical current to the second hypoglossal nerve; and (4) circuitry configured to, in response to a detected symmetry-related factor indicative of a degree of symmetry of the subject, configure at least one current selected from the group consisting of: the first current and the second current. Other embodiments are also described. | 2015-02-05 |
| 20150039047 | PHYSICIAN PROGRAMMER WITH ENHANCED GRAPHICAL USER INTERFACE, AND ASSOCIATED SYSTEMS AND METHODS - Devices for controlling spinal cord modulation for inhibiting pain, and associated systems and methods, including controllers for modulation program recommendation are disclosed. A particular embodiment includes receiving, from multiple computing devices, ratings for modulation programs executed by implantable medical devices for a plurality of patients, ranking the modulation programs based on the received ratings and based on at least one characteristic of the patients and the symptoms described by the patients, receiving a recommendation request for a modulation program for a particular patient; and transmitting one or more of the highest ranking modulation programs in response to the request for a modulation program for the particular patient. | 2015-02-05 |
| 20150039048 | IMPLANTABLE PULSE GENERATOR HAVING CURRENT STEERING MEANS - An implantable pulse generator includes a current steering capability that allows a clinician or patient to quickly determine a desired electrode stimulation pattern, including which electrodes of a group of electrodes within an electrode array should receive a stimulation current, including the amplitude, width and pulse repetition rate of such current. Movement of the selected group of electrodes is facilitated through the use of remotely generated directional signals, generated by a pointing device, such as a joystick. As movement of the selected group of electrodes occurs, current redistribution amongst the various electrode contacts takes place. The redistribution of stimulus amplitudes utilizes re-normalization of amplitudes so that the perceptual level remains fairly constant. This prevents the resulting paresthesia from falling below the perceptual threshold or above the comfort threshold. | 2015-02-05 |
| 20150039049 | SELECTIVE HIGH FREQUENCY SPINAL CORD MODULATION FOR INHIBITING PAIN WITH REDUCED SIDE EFFECTS, AND ASSOCIATED SYSTEMS AND METHODS - Selective high-frequency spinal cord modulation for inhibiting pain with reduced side affects and associated systems and methods are disclosed. In particular embodiments, high-frequency modulation in the range of from about 1.5 KHz to about 50 KHz may be applied to the patient's spinal chord region to address low back pain without creating unwanted sensory and/or motor side affects. In other embodiments, modulation in accordance with similar parameters can be applied to other spinal or peripheral locations to address other indications. | 2015-02-05 |
| 20150039050 | SELECTIVE HIGH FREQUENCY SPINAL CORD MODULATION FOR INHIBITING PAIN WITH REDUCED SIDE EFFECTS, AND ASSOCIATED SYSTEMS AND METHODS - Selective high-frequency spinal cord modulation for inhibiting pain with reduced side affects and associated systems and methods are disclosed. In particular embodiments, high-frequency modulation in the range of from about 1.5 KHz to about 50 KHz may be applied to the patient's spinal chord region to address low back pain without creating unwanted sensory and/or motor side affects. In other embodiments, modulation in accordance with similar parameters can be applied to other spinal or peripheral locations to address other indications. | 2015-02-05 |
| 20150039051 | Functional Electrical Stimulation Device and System, and Use Thereof - A functional electrical stimulation (FES) device and system. In one embodiment, sequential bipolar pulse stimulation may be provided to an area of a living body via one or more electrode leads applied to the area via a FES device comprising a current pulse generating circuit comprising output nodes for operative coupling to the one or more electrode leads, and configured for operative coupling to a voltage supply. The current pulse generating circuit generally comprises positive and negative stimulation paths drawing from the voltage supply to respectively apply positive and negative currents through the area via the one or more electrode leads. In one example, the stimulation paths comprise respective capacitive elements, a capacitance ratio of which dictating, at least in part, an amplitude ratio of the positive and negative currents, wherein periodic alternative activation of the stimulation paths provides the sequential bipolar pulse stimulation. | 2015-02-05 |
| 20150039052 | RECOGNITION OF IMPLANTABLE MEDICAL DEVICE - Controlling the interaction between an external device and an implanted device, including a method of controlling interaction between an external device and an implanted device, the method including at least the steps of: establishing communications between the implanted device and the external device; the external device determining an identification of the implant and comparing the identification with identifications in a stored list; if the device matches one of said identifications, then using a corresponding set of operating parameters to interact with said implant; and otherwise, not interacting with said device. | 2015-02-05 |
| 20150039053 | SYSTEMS AND METHODS OF DELIVERING THERAPY USING AN AMBULATORY MEDICAL DEVICE - An ambulatory medical device capable of delivering therapy to a patient is provided. The ambulatory medical device comprises at least one controller operatively connected to at least one sensor configured to detect a health disorder of the patient, at least one treatment element configured to deliver therapy to the patient, and at least one response mechanism configured to be actuated by the patient, the at least one response mechanism having one of a first state and a second state. The at least one controller being configured to delay delivery of the therapy to patient for a first predetermined period of time responsive to detection of the health disorder and the at least one response mechanism having the first state, and to deliver the therapy to the patient in response to continued detection of the health disorder, the at least one response mechanism remaining in the first state. | 2015-02-05 |
| 20150039054 | IMPLANTABLE MEDICAL DEVICE WHICH MAY BE CONTROLLED FROM CENTRAL STATION - An implantable medical device (IMD) comprises a transmitting/receiving (T/R) device for transmitting medical data sensed from a patient to, and for receiving control signals from, a medical expert (a human medical professional and/or a computerized expert system) at a remote location; an electronic medical treatment device for treating the patient in response to control signals applied thereto; and a sensor circuit, having a sensor circuit output, for producing sensor circuit output signal(s) representing medical data sensed from the patient. The IMD also includes a logic device (processor) which analyzes the sensor circuit output signal(s) to detect a medical abnormality and, upon detecting an abnormality, either sends a notification signal representing a medical state of said patient to the medical expert at the remote location or sends a local treatment device control signal to the medical treatment device, or does both. The medical expert can transmit an external treatment control signal to the IMD to effect patient treatment, if treatment is warranted. To ensure that the medical expert is authorized to provide such treatment, data which identify one or more authorized medical experts is stored in an IMD memory and compared with identification data transmitted from the putative authorized medical expert along with the external treatment control signal. Only if the identification data received from the putative authorized medical expert matches the pre-stored identification data of an originally authorized medical expert does the IMD effect treatment. | 2015-02-05 |
| 20150039055 | INTERFACE APPARATUS FOR STIMULATION OF BIOLOGICAL TISSUE - An apparatus for interfacing between tissues being stimulated is provided. The apparatus includes an electric source capable of generating an applied electric field across a region of tissue and/or a means for altering at least one electromagnetic characteristic of the region of tissue relative to the applied electric field and an interface component, such interface component creating an interface between the region of tissue and the applied electric field or the means for altering at least one electromagnetic characteristic of the region of tissue. | 2015-02-05 |
| 20150039056 | Insert Tool for Selectively Powering an Implant Unit - An implant unit delivery tool is disclosed having an implant tool and an implant activator. The implant tool may be configured to retain an implant unit during an implantation procedure in which the implant unit is fixated to tissue. The implant activator may be associated with the implant tool. Additionally, the implant activator may be configured to selectively transfer power to the implant unit during the implantation procedure to cause modulation of at least one nerve in the body of a subject prior to final fixation of the implant unit to the tissue. | 2015-02-05 |
| 20150039057 | IMPLANTABLE VESTIBULAR PROSTHESIS - An implantable nerve stimulation device has a sensor system, a data processor in communication with the sensor system, and a nerve stimulation system in communication with the data processor and constructed to provide electrical stimulation to at least one branch of at least one vestibulocochlear nerve. The nerve stimulation system includes an electrode array that has a first plurality of electrodes structured to be surgically implanted in electrical communication with a superior branch of the vestibular nerve, a second plurality of electrodes structured to be surgically implanted in electrical communication with a horizontal branch of the vestibular nerve, a third plurality of electrodes structured to be surgically implanted in electrical communication with a posterior branch of the vestibular nerve, and a common crus reference electrode structured to be surgically implanted into a common crus of the vestibular labyrinth. | 2015-02-05 |
| 20150039058 | SYSTEM AND METHOD FOR NEUROMODULATION - A method of treating autonomic imbalance in a patient includes energizing a first therapeutic element disposed to deliver therapy to a parasympathetic nerve fiber (e.g. vagus nerve), and energizing a second therapeutic element to deliver therapy to a sympathetic cardiac nerve fiber. At least one of the therapeutic elements is disposed in the vasculature superior to the heart. The therapy decreases the patient's heart rate and elevates or maintains the blood pressure of the patient. | 2015-02-05 |
| 20150039059 | GUIDE CATHETER HAVING VASOMODULATING ELECTRODES - A guide catheter system includes a guide catheter having a proximal end, a distal end, an outer wall and a first, second and third electrode wherein the first, second and third electrodes are spaced longitudinally apart from each other on the outer wall of the catheter, and an electrical impulse generator connected to the guide catheter wherein the electrical impulse generator includes a circuit for selecting an adjacent pair of electrodes to use as a bipolar electrode system to send an electrical impulse and a method of use thereof to treat vasospasm. | 2015-02-05 |
| 20150039060 | WEARABLE AND BREATHABLE PHOTO THERAPY PATCH - A radiation device ( | 2015-02-05 |
| 20150039061 | DISPLAY APPARATUS PROVIDING LIGHT THERAPY - A display apparatus providing light therapy includes a display panel configured to display an image to a display region based on input image data, and a lens part disposed on the display panel, the lens part configured to focus the image displayed by the display panel toward a first region in a therapy mode, in which the first region is smaller than the display region, and the first region may correspond to a position of a user's face. | 2015-02-05 |
| 20150039062 | WARMING DEVICE FOR PERIOPERATIVE USE - A warming device for perioperative use includes a clinical garment and a convective thermal blanket supported on an inside surface of the clinical garment. A mechanism may be provided to releasably attach the thermal blanket to the clinical garment. | 2015-02-05 |
| 20150039063 | APPARATUSES AND METHODS FOR SECURING DEEP BRAIN STIMULATION LEADS - Various examples are provided for securing deep brain stimulation (DBS) leads. In one example, among others, a DBS cap for securing a DBS lead includes a base ring adapted to be mounted within a counterbore opening formed in the skull, a lead securing element that mounts to the base ring, and a top cover that mounts to the base ring. In another example, a method for securing a DBS lead includes forming a counterbore opening in the skull, securing a DBS cap within the counterbore opening, passing a DBS lead through the DBS cap and the counterbore opening and positioning a tip of the lead in brain tissue, and securing the DBS lead to the DBS cap using an adhesive. The skull opening includes a lower bore, a concentric upper bore, and a step positioned at the interface of the upper and lower bores. | 2015-02-05 |
| 20150039064 | LEAD ELECTRODE FOR USE IN AN MRI-SAFE IMPLANTABLE MEDICAL DEVICE - A medical lead is configured to be implanted into a patient's body and comprises a lead body, and an electrode coupled to the lead body. The electrode comprises a first section configured to contact the patient's body, and a second section electrically coupled to the first section and configured to be capacitively coupled to the patient's body. | 2015-02-05 |
| 20150039065 | PACING LEADS WITH ULTRATHIN ISOLATION LAYER BY ATOMIC LAYER DEPOSITION - An implantable medical lead includes a substrate extending from a distal end to a proximal end of the medical lead. The substrate includes at least one polymer material and particles dispersed throughout the polymer material. In one embodiment, the particles are of at least one of nanoclay material and nanodiamond material. | 2015-02-05 |
| 20150039066 | SYSTEMS, METHODS AND DEVICES FOR A SKULL/BRAIN INTERFACE - Systems, methods and devices are disclosed for directing and focusing signals to the brain for neuromodulation and for directing and focusing signals or other energy from the brain for measurement, heat transfer and imaging. An aperture in the skull and/or a channel device implantable in the skull can be used to facilitate direction and focusing. Treatment and diagnosis of multiple neurological conditions may be facilitated with the disclosed systems, methods and devices. | 2015-02-05 |
| 20150039067 | Retinal Prosthesis with Multiple Electrode Arrays for Greater Field of View - The artificial percept of light may be created by electrically stimulating the neurons of the retina. While a photolithographed array internal to the retina provides superior resolution, an array external to the retina provides easier implantation and improved manufacturability. Therefore it is advantageous to supply a high-resolution electrode array internal to the sclera, near the fovea and a lower-resolution electrode array eternal to the sclera near the periphery of the retina. | 2015-02-05 |
| 20150039068 | LEADS WITH ELECTRODE CARRIER FOR SEGMENTED ELECTRODES AND METHODS OF MAKING AND USING - A stimulation lead includes a lead body having a longitudinal length, a distal portion, and a proximal portion; terminals disposed along the proximal portion of the lead body; an electrode carrier coupled to, or disposed along, the distal portion of the lead body; segmented electrodes disposed along the electrode carrier; and conductors extending along the lead body and coupling the segmented electrodes to the terminals. The electrode carrier includes a lattice region defining segmented electrode receiving openings. Each of the segmented electrodes extends around no more than 75% of a circumference of the lead and is disposed in a different one of the segmented electrode receiving openings of the electrode carrier. | 2015-02-05 |
| 20150039069 | FIXATION FOR IMPLANTABLE MEDICAL DEVICES - A tine portion for an implantable medical device includes a hook segment and a distal segment terminated by a tissue-piercing tip, wherein the distal segment extends from the hook segment to the tip. The hook segment, which is elastically deformable from a pre-set curvature, has one of: a round cross-section and an elliptical cross-section, while the distal segment has a flattened, or approximately rectangular cross-section. One or a pair of the tine portions may be integrally formed, with a base portion, from a superelastic wire, wherein the base portion is configured to fixedly attach to the device, for example, being captured between insulative members of a fixation subassembly. | 2015-02-05 |
| 20150039070 | FIXATION FOR IMPLANTABLE MEDICAL DEVICES - A tine portion of an implantable medical device includes a hook segment and a distal segment terminated by a tissue-piercing tip, wherein the distal segment extends from a distal end of the hook segment to the tip. The hook segment, which is elastically deformable from a pre-set curvature, for example, defined by a single radius, preferably tapers from a first width thereof, in proximity to a proximal end thereof, to a smaller, second width thereof, in proximity to the distal end thereof, wherein the tip has a width that is greater than the second width of the hook segment. Alternately, the tine portion may include a hook segment that is defined by two radii and a straight section extending therebetween. | 2015-02-05 |
| 20150039071 | FIXATION FOR IMPLANTABLE MEDICAL DEVICES - A tine portion of an implantable medical device includes a hook segment and a distal segment extending therefrom, wherein the hook segment is pre-set to extend along a curvature and is elastically deformable therefrom to an open position. The distal segment includes a tooth and an end that surrounds the tooth, wherein the end includes a pair of legs and a distal arch. The legs extend along a length of, and on opposing sides of the tooth, and the distal arch extends between the legs, distal to a tissue-piercing tip of the tooth. When the hook segment is in the open position, and a force is applied along a longitudinal axis of the device, to push the distal arch of the distal segment against tissue, for initial tissue penetration, the legs of the end of the distal segment bend in elastic deformation to expose the tissue-piercing tip to the tissue. | 2015-02-05 |
| 20150039072 | FLEXIBLE STENT - The stent of the present invention combines a helical strut band interconnected by coil elements. This structure provides a combination of attributes that are desirable in a stent, such as, for example, substantial flexibility, stability in supporting a vessel lumen, cell size and radial strength. The structure of the stent of the present invention provides a predetermined geometric relationship between the helical strut band and interconnected coil elements in order to maintain connectivity at any diameter size state of the stent. | 2015-02-05 |
| 20150039073 | STENT FOR BIFURCATION, A SYSTEM FOR INTRAVASCULAR IMPLANTATION OF THE STENT FOR BIFURCATION AND A METHOD OF IMPLANTATION OF THE STENT FOR BIFURCATION - A stent for bifurcation, including two cylindrical parts: a distal part ( | 2015-02-05 |
| 20150039074 | VASCULAR PROSTHESIS FOR TREATING ANEURYSMS - Apparatus for use with a delivery catheter, including a primary stent-graft and a flared endovascular stent-graft, which is configured to initially be positioned in the delivery catheter in a radially-compressed state, and to assume a radially-expanded state upon being deployed from the delivery catheter. The primary stent-graft includes (a) a structural member, which includes a plurality of structural stent elements, and which, when the flared endovascular stent-graft assumes the radially-expanded state, is shaped so as to define a flared caudal portion, which flares radially outward in a caudal direction; (b) at least one biologically-compatible substantially fluid-impervious flexible sheet, which is coupled to at least the flared caudal portion; and (c) a stent-engagement member, which is generally tubular when the flared endovascular stent-graft assumes the radially-expanded state, which is disposed at least partially within the flared caudal portion, and which is configured to be sealingly coupled to the primary stent-graft. | 2015-02-05 |
| 20150039075 | VARIABLE STIFFNESS STENT - A stent has one or more redundant crests for a ring. The redundant crest is located at a Y-crown for a peak-to-valley type stent pattern in one example. The stent may also have frangible bridges for connecting links. The stent's radial stiffness decreases when a redundant crest fractures and its axial and bending stiffness decreases when a frangible bridge breaks. | 2015-02-05 |
| 20150039076 | One-Way Heart Assist Valve - A medical device used in patients with inefficient heart function to improve the efficiency of the pumping action of the heart. This device adds one or more one-way valves in the blood vessels and/or arteries, very near, but not in, the heart, thereby increasing the efficiency of the native heart. The device includes one or more one-way heart valves designed to go in arteries/veins that are connected to the heart, and which arteries and/or veins are the conduits for taking blood into/out of the heart. The one-way heart valve allows blood flow in only one direction. An optional sleeve (stent) may be placed outside the arteries/veins where the valve(s) are located to add support to the walls. An optional sleeve (stent) may also be used on the inside of the artery to insure the artery does not collapse during a vacuum phase of the beating. | 2015-02-05 |
| 20150039077 | MEDICAL DEVICES INCLUDING METALLIC FILM AND AT LEAST ONE FILAMENT - Medical devices, such as endoprostheses, and methods of making the devices are disclosed. The medical device can include a composite cover formed of a deposited metallic film. The cover may include one or more filaments, e.g., wires, which cooperate with the film to provide desirable mechanical properties. The wires may be integrated with the film by depositing the film over the wires. | 2015-02-05 |
| 20150039078 | HIGHLY FLEXIBLE STENT AND METHOD OF MANUFACTURE - Preferred embodiments of a stent with a high degree of flexibility are shown and described. The stent can include a continuous helical winding having interconnected struts joined at vertices, and having bridges connecting sections of the helical winding to each other. An annular ring can be provided at one or both ends of the helical winding, and the annular ring can have extensions extending to connect to the helical winding. One of the extensions can connect to a bridge and another extension can connect to a vertex. The struts at the ends of the helical winding can have strut lengths that differ from the strut lengths of the struts in a central portion of the winding between the ends of the winding. | 2015-02-05 |
| 20150039079 | DEVICES AND METHODS FOR ASSISTING VALVE FUNCTION, REPLACING VENOUS VALVES, AND PREDICTING VALVE TREATMENT SUCCESS - Devices and methods for assisting valve function, replacing venous valves, and predicting valve treatment successes. In at least one exemplary embodiment of an endograft body configured for expansion within a luminal organ of the present disclosure, the endograft body comprises (a) a first portion having a proximal end defining a proximal end aperture and a distal end defining a distal end aperture, the first portion configured to increase a velocity of fluid flowing therethrough, (b) a second portion having a second portion proximal end defining a second portion proximal end aperture and a second portion distal end defining a second portion distal end aperture. | 2015-02-05 |
| 20150039080 | IMPLANT FOR BUNDLING A PLURALITY OF TENDONS, PARTICULARLY CHORDAE TENDINEAE - The present invention relates to an implant for bundling a plurality of tendons, particularly chordae tendineae, wherein a three-dimensionally curved element, revolves around a central axis at a radius with respect to the central axis and wherein said radius is larger at a first portion of said curved element than at a second portion of said curved element and wherein said curved element is designed to encompass said plurality of tendons and to bundle them, causing an effective shortening of the tendons along the central axis of the curved element. | 2015-02-05 |
| 20150039081 | Mitral Valve Prosthesis for Transcatheter Valve Implantation - A transcatheter valve prosthesis is disclosed that has a compressed, delivery configuration and an expanded configuration for deployment within a native heart valve. The valve prosthesis includes a self-expanding frame and a prosthetic valve component. The self-expanding frame includes a valve receiving portion defining an opening therethrough and first and second anchors at opposing ends of the valve receiving portion. The valve receiving portion is substantially planar and the first and second anchors are oriented substantially perpendicular to the valve receiving portion when the valve prosthesis is in the expanded configuration. The prosthetic valve component is disposed within the opening of the valve receiving portion and secured thereto. | 2015-02-05 |
| 20150039082 | Arrangement, A Loop-Shaped Support, A Prosthetic Heart Valve And A Method Of Repairing Or Replacing A Native Heart Valve - The present disclosure relates to an arrangement, a loop-shaped support, a prosthetic heart valve and a method of repairing or replacing a native heart valve. With the method or the arrangement, leakage or regurgitation between a prosthetic heart valve and the surrounding valve tissue is prevented. In one embodiment, an arrangement for replacement or repair of a native heart valve is provided, which comprises a loop-shaped support ( | 2015-02-05 |
| 20150039083 | DEVICES, SYSTEMS AND METHODS FOR REPAIRING LUMENAL SYSTEMS - The disclosure provides systems and related methods for delivering a prosthesis to a target location. Various embodiments of useful valve prostheses are also disclosed. | 2015-02-05 |
| 20150039084 | Heart Anchor Device - A medical implant including an anchor portion including a plurality of arms adapted to engage an internal tissue wall of a body from two opposite faces, wherein the anchor portion is configured such that at least one of the arms does not have an entirely overlapping arm on the other side of the wall and an opening portion adapted to define an opening for blood flow through the internal tissue wall, when the anchor portion engages the wall. | 2015-02-05 |
| 20150039085 | Expandable Surgical Implant Device - A surgical implant device may include a first substantially planar portion having a first surface area, a second substantially planar portion having a second surface area, and a coupling device for connecting the first substantially planar portion to the second substantially planar portion. The coupling device facilitates expanding and contracting the first and the second substantially planar portion in order to provide an implant surface area corresponding to the first surface area during insertion of the surgical implant within an incision, and having a third surface area corresponding to both the first surface area and at least a portion of the second surface area following insertion of the surgical implant within the incision. | 2015-02-05 |
| 20150039086 | IMPLANTABLE MICRO-TEXTURED SCAR INDUCING ePTFE STRUCTURES - Bio-implantable textured tubular and sheet structures of un-sintered ePTFE are described. Such micro-textured structures stimulate robust development of beneficial bio-integative scar attachment to adnexal soft tissues. Methods for texturing one side of an un-sintered extruded ePTFE tube or sheet are also described. A select length of tubing of any thickness or diameter is applied over a matching mandrel and adhesively stabilized thereon by applying intense suction. The texture is made by “RIGDA tooling” into the wall thickness of the material and by removing undesired material by distraction and avulsion tooling and methods assisted by vibration, leaving intact the finished product. Disclosed is an implantable, non-attached, enveloping, conforming and supportive drainage cover for breast and other soft implants. The drainage cover has numerous through and through cut lucencies which allow for liberal ingress and egess of interstitial biologic fluids enabling efficient drainage postoperatively, especially under the influence of active wound suction. | 2015-02-05 |
| 20150039087 | Method of Designing Custom Device for Alleviating Temporomandibular Joint-Related Symptoms - An in-ear device with one or more proprioceptive features for providing an indication to a subject to help manage or reduce pain, discomfort, or other symptoms associated with TMJ disorder. Also disclosed are methods of using optical scanning to create a three dimensional replication of the ear canal that is used to design a customized in-ear device. In some embodiments, the in-ear device is customized based on the configuration of the subject's ear canal when the subject's jaw is in the therapeutic or optimal position. | 2015-02-05 |
| 20150039088 | MIDDLE EAR PROSTHESIS - A middle ear prosthesis ( | 2015-02-05 |
| 20150039089 | Artificial Disc Devices and Related Methods of Use - An artificial disc is disclosed. The artificial disc may include a superior endplate having a bi-convex superior surface and a concave inferior surface, and an inferior endplate having a bi-convex inferior surface. The artificial disc may also include a core assembly disposed between the superior endplate and the inferior endplate, and a support assembly disposed on outer surfaces of both the superior endplate and the inferior endplate. The support assembly may be configured to couple the superior endplate to the inferior endplate. | 2015-02-05 |
| 20150039090 | SYSTEMS AND METHODS FOR VERTEBRAL DISC REPLACEMENT - The present invention provides artificial disc prostheses, methods and instrumentation for implantation and revision thereof. Each prosthesis may comprise superior and inferior end plates and a nucleus positioned between articular surfaces of the end plates. The end plates may have planar bone engagement surfaces with a plurality of self-cutting teeth. The articular surfaces of the end plates may be planar or include a flattened portion. The nucleus includes superior and inferior articular surfaces which may comprise flattened portions such that when the articular surfaces of the nucleus and the end plates are placed in cooperation in a preferred orientation, the flattened and/or planar portions are aligned. Each prosthesis may provide flexion/extension, anterior/posterior translation, lateral bending, and/or axial rotation degrees of freedom. One embodiment comprises a prosthesis with a first joint providing flexion/extension and anterior/posterior translation, and a second joint providing lateral bending and axial rotation. | 2015-02-05 |
| 20150039091 | CONSTRAINED MOBILE BEARING HIP ASSEMBLY - An acetabular hip implant includes an acetabular shell component having a first feature and a first insert having a second feature that cooperates with the first feature of the acetabular shell component and further includes a third feature. The implant further includes a second insert having a fourth feature that cooperates with the third feature of the first insert and further includes a fifth feature. A femoral head component includes a sixth feature that cooperates with the fifth feature. Interaction between the first and second features, between the third and fourth features, and between the fifth and sixth features mechanically constrains the acetabular hip implant to prevent dislocation of the femoral head during rotation. | 2015-02-05 |
| 20150039092 | MUCOSAL CAPTURE FIXATION OF MEDICAL DEVICE - A medical device adapted to be fixed in a hollow organ or cavity lined with mucosa includes a wall having an outer surface with a size and shape that is configured to a portion of a cavity or hollow organ lined with mucosa and a fixation mechanism. The fixation mechanism is adapted to fix the wall with the portion of the cavity or hollow organ. The fixation mechanism has at least two adjacent openings in the wall between proximal and distal ends of the wall. The openings being large enough to receive a section of the mucosa extending in the openings when said wall is positioned in the hollow organ or cavity. The openings are separated by a bridge and are close enough together that the mucosa that extends into the openings comes together over the bridge to fix the medical device in the hollow organ or cavity. | 2015-02-05 |
| 20150039093 | DIFFERENTIAL POROSITY PROSTHETIC SYSTEM - A prosthetic femoral implant for use in a hip joint, as a ball and socket type joint, is disclosed. The implant includes a modular neck having a variety of adjustable positions to adjust the lateral offset and version angle of the femoral implant in relation to the femur. The implant further includes a broad, full collar for providing a compression force increasing the interdigitation between the interface of the bone, implant and cement. The implant also includes a stem having a depression having a roughened porous surface for resisting the increased torsional loads placed on the implant due to the increased lateral offset and version angle. The stem further comprises three distinct zones, each zone having its own roughened surface creating a tripartite differential porosity. | 2015-02-05 |
| 20150039094 | CEMENT-FREE SURFACE REPLACEMENT PROSTHESIS FOR THE NATURAL FEMUR HEAD - The invention relates to a ceramic surface replacement prosthesis (I) for the natural femur head ( | 2015-02-05 |
