Abstract: A mechanical grasping device where each of the segments of the finger assemblies, are individually sizeable. This allows for both a proportionately scalable grasping device as well as individual customization of geometric configurations tailored to specific use patterns. The mechanical grasping device is crushable since it has flexible and pivotable connections between digits along its length and width. It has a hollow member construction that imparts a strong lightweight design. It is modular so individual parts can be replaced for quick repair. From an aesthetics point, it is visually pleasing and can be offered in different colors, and with custom digit sleeves for specific applications. Finger assemblies can be operated individually or in groups via pairs of cables which allow operation in either voluntary open or voluntary closed modes of control. The flexible construction allows gripping of irregularly shaped objects and deforms before failing giving indication of overload prior to failure.

Abstract: A prosthetic foot with a structural component having a proximal attachment member for fastening the prosthetic foot to a below-knee tube, a below-knee shaft or a prosthetic knee joint, with a forefoot portion secured or formed on the structural component, and with a heel-side spring-damper system which is assigned to the structural component and which is compressed at a heel strike and bears on a sole-side guide element. The structural component is designed as a leaf spring which extends in a posterior direction from the proximal attachment means, and forms an arch and is guided in an anterior and distal direction, wherein the arch protrudes posteriorly beyond the guide element.

Abstract: A stem for fixating a prosthesis to a bone can include a first stem portion and a second stem portion. The first stern portion can extend substantially along a longitudinal axis. The first stem portion can include a distal portion. The second stem portion can extend substantially distally from the distal portion of the first stem portion along the longitudinal axis. The second stem portion can be securable to the bone, and the second stem portion can include a distal portion couplable to a compress assembly.

Abstract: A prosthetic foot comprising a vacuum system configured to attach to a vacuum attachment apparatus and a residual limb. The prosthetic foot may comprise a resilient bottom member, a resilient top member, and a vacuum system. The resilient bottom member may comprise a front end and a rear end. The resilient top member may comprise a front end and a rear end and the front end of the resilient top member may be connected to the front end of the resilient bottom member. The vacuum system may be coupled to an underside of the rear end of the top member. The vacuum system may comprise a compressible member, a chamber located within the compressible member, a valve system received within the compressible member, a passageway connecting the valve system and the chamber, and an air return coupled to the valve system and the vacuum attachment apparatus.

Abstract: A motion assist device includes a drive mechanism that applies a force to the body of a user through the intermediary of a first orthosis and a second orthosis, posture detectors that detect the posture of the user, and a control unit that controls the drive mechanism. A transmission mechanism of the drive mechanism is configured to be switchable between a transmission mode, in which a driving force based on a spring is transmitted to move a joint into a predetermined state, and a non-transmission mode, in which a joint can be freely moved without transmitting the driving force that has been accumulated. The control unit automatically switches the transmission mechanism to the non-transmission mode when a predetermined trigger event is recognized based on the posture of the user.

Abstract: Core for a spacer, including a main body that comprises a plurality of through openings, adapted to be secured in a corresponding residual bone bed of a previous implant; the main body being adapted to be covered with a layer (S) of a coating material or a material including acrylic bone cement added or that can be added with one or a plurality of pharmaceutical products or active and/or therapeutic substances.

Abstract: The present disclosure provides a shoulder prosthesis. The shoulder prosthesis includes a glenoid component, a humeral component, and an articulation component. The glenoid component includes a glenoid body having a proximal side and a distal side, the proximal side shaped to engage with a resected portion of a glenoid cavity. The humeral component includes a humeral body having a proximal side and a distal side, the distal side shaped to engage with a resected portion of a humerus. The articulation component is positionable between the distal side of the glenoid component and the proximal side of the humeral component, the articulation component configured to be maintained between the glenoid and humeral components, after implantation, by at least one of a deltoid muscle and a rotator cuff.

Abstract: The invention features acetabular components for an artificial hip. The invention also features methods and tools for assembling a hip prosthesis that includes the acetabular components of the invention.

Abstract: The use of lipids in the taper junction or other metal on metal interface of a modular orthopedic implant to prevent fretting corrosion and increase the pull off load. The incorporation of lipids or a lipid-like substrate within the taper junction increases the onset load and decreases the amount of corrosion. The incorporation of lipids also increases the pull-off load necessary to separate the head from the neck. As a result, the use of lipids in the taper junction of an orthopedic implant should reduce the need for revisions of implants, such as such as knee and hip replacements, which are often needed because of fretting corrosion.

Abstract: The present disclosure provides a shoulder prosthesis. The shoulder prosthesis includes a glenoid component, a humeral component, and an articulation component. The glenoid component includes a glenoid body having a proximal side and a distal side, the proximal side shaped to engage with a resected portion of a glenoid cavity. The humeral component includes a humeral body having a proximal side and a distal side, the distal side shaped to engage with a resected portion of a humerus. The articulation component is positionable between the distal side of the glenoid component and the proximal side of the humeral component, the articulation component configured to be maintained between the glenoid and humeral components, after implantation, by at least one of a deltoid muscle and a rotator cuff.

Abstract: An implant for attachment to a human pelvic bone for cosmetic purposes. The implant is attachable to the iliac crest. A silicone cover is attachable to the implant. Implant plates may be attached to the humeral bone, the tibia, and the femur, and silicone may be attached to the plates.

Abstract: An orthopaedic prosthetic includes a femoral component including a pair of condyles spaced apart to define an intercondylar notch. A tibial component includes a tray and a platform pivotally coupled to the tray. A modular insert is configured to be selectively coupled to the femoral component to couple the femoral component to the tibial component.

Abstract: Semi-passive control system (10) comprises a pneumatic spring actuator (16), a pressure regulator (22) in communication with the pneumatic spring actuator (16), a hydraulic locking actuator (18), a hydraulic valve (20) in communication with actuator (18), a power source (14), a pulley wheel (42), and a cable (46) having a first end in contact with pulley wheel (42), first and second side portions (50, 56) extending from opposing sides of pulley wheel (42), and a second end adapted to connect to an orthosis device (76). At least one cable clamp (62) attaches to second side portion (56) of cable (46) and interconnects cable (46) to shafts (112b, 118b) of actuators (16, 18). A central control unit (12) includes a processor (13a) and a computer readable storage medium (13b) having program instructions stored thereon for execution by the central control unit to adjust stiffness, damping or stiffness and damping parameters.

Abstract: A magnetic locking actuator for a prosthetic or orthotic device is provided. The actuator includes a first component including one or more magnets and a second component including one or more magnets. The first and second components are coupled to separate portions of the device. The magnets allow for adjustment of a length of the actuator to adjust an angular orientation of the first and second portions of the device. When magnets in the second component are aligned with magnets in the first component having an opposite polarity, a position of the second component is fixed relative to the first component, locking the actuator. When magnets in the second component are not aligned with magnets in the first component having the opposite polarity, the position of the second component is adjustable relative to the first component, thereby allowing adjustment of the height of the actuator.

Abstract: An orthopaedic surgical instrument system includes a tibial base trial and a tibial insert trial. An insert adaptor is sized to be positioned in an aperture defined in the tibial insert trial. The insert adaptor includes a base sized to be positioned over a post of the tibial base trial and a locking tab positioned in the base and configured to engage the post of the tibial base trial.

Abstract: A bone graft containment device includes a body extending longitudinally from a first end to a second end. The body includes a channel extending longitudinally therethrough. The device also includes a fluid delivery structure received within the channel. The fluid delivery structure includes a central tubular member extending along a length of the channel and a laterally extending tubular member extending laterally from the central tubular member to a fluid receiving opening. The central tubular member includes a plurality of openings extending laterally through a wall thereof, so that, when the fluid receiving opening is connected to an external fluid source, fluid is passed through the laterally extending tubular member and the central tubular member to be dispersed to a graft material packed within the channel via the plurality of openings.

Abstract: The present disclosure relates to prosthesis systems having trays and liners having an asymmetrical locking mechanism to bias the strength of the liner to resist loading forces and associated methods. The tray has a lateral groove disposed in an inner surface of a lateral circumferential portion of the tray and a medial groove disposed in an inner surface of a medial circumferential portion of the tray. The liner has an upper segment and a lower segment. The liner has a locking portion for lockingly engaging the tray that includes the lower segment. The locking portion has a lateral toe positioned generally diametrically opposite a plurality of resiliently deformable medial fingers defined therein. The liner and the tray are engageable in a lateral-to-medial direction so that the plurality of medial fingers can resiliently deform to engage the medial groove subsequent to engagement of the lateral toe within the lateral groove.

Abstract: A tibial insert includes a base and a post extending from the base along a longitudinal axis. The post has a medial surface, a lateral surface, a height along the longitudinal axis, and a rotational offset in a superior-inferior aspect of the post. The medial surface has a medial section, and the lateral surface has a lateral section oriented substantially parallel to the medial section. The medial section and the lateral section each have a width in a substantially anterior-posterior direction that is sufficient to enable varus/valgus constraint over a flexion/extension range from extension to about 90 to 120 degrees of flexion when the tibial insert is mated with a femoral component.

Abstract: A compression stabilized prosthetic device for a patient having an amputated limb includes a first socket portion for contacting a patient's limb, and a second portion for the attachment of a prosthetic component. The first socket portion has compression portions configured for compressing portions of the patient's limb, and relief portions for receiving other portions of the patient's limb which bulge upon the compression applied by the compression portions. The relief portions may be formed as openings or as enlarged radius portions of the first socket portion.

Abstract: Prosthetic devices and methods of controlling the same are provided. A prosthetic ankle device includes a foot unit and lower limb member moveable relative to one another and defining an ankle angle therebetween. The prosthetic ankle device further includes a controller to operate the device based on weight shifting. Methods of controlling the prosthetic ankle device include operating the device at different ankle angles depending on weight shifting of the user while standing or stopped.