Abstract: A method for reconstructing a joint according to an exemplary aspect of the present disclosure includes, among other things, fixating at least one suture inside a joint space, retrieving the at least one suture from inside the joint space, passing the at least one suture through a graft at a location external to the joint space, shuttling the graft into the joint space, and fixating the graft using the at least one suture.

Abstract: Implantable medical devices are provided. In one embodiment, a device includes a body having an external surface defining an outer profile of the device. The body includes a porous matrix including a series of interconnected macropores defined by a plurality of interconnected struts each including a hollow interior. A filler material substantially fills at least a portion of the series of interconnected macropores. The external surface of the body includes a plurality of openings communicating with the hollow interior of at least a portion of the plurality of interconnected struts. In a further aspect of this embodiment, the external surface includes exposed areas of the filler material and porous matrix in addition to the exposed openings. In another aspect, the porous matrix is formed from a bioresorbable ceramic and the filler material is a biologically stable polymeric material. Still, other aspects related to this and other embodiments are also disclosed.

Abstract: Mandible endoprosthesis implant and mandible endoprosthesis implant system and surgical kit comprising the same, the mandible endoprosthesis implant comprising: first end second implant elements which can be coupled in a manner so as to allow a relative pivotal movement therebetween. The present disclosure further provides methods for surgically repairing a mandible.

Abstract: An osseointegratable prosthetic device suitable for implantation via a one-step surgical process includes a threaded insertion end, an externally accessible tool interface end, and an intermediately arranged scaffold portion defining recesses that permit ingrowth of skeletal tissue. Such recesses may include multiple longitudinal fins as well as transverse ribs, which may embody or be coated with porous material to promote bone ingrowth. A split flange portion includes discontinuous portions and may permit pretensioning of the device. The device may be fabricated as a unitary body structure from thermoplastic materials using techniques such as fused filament fabrication (a form of 3D printing). The osseointegratable prosthetic device enables one-step surgical implantation without requiring separately implantable fixture/sleeve and abutment portions according to conventional osseointegratable prosthetics. Methods for fabricating an osseointegratable prosthetic device are further provided.

Abstract: Acetabular prosthesis comprising an acetabular cup, an acetabular insert, able to be stably coupled inside the acetabular cup and configured to receive an articulation head and a centering unit configured to guide and center the insertion and stable positioning of the acetabular insert in the acetabular cup. The centering unit comprises a centering hole provided in the acetabular cup and a centering pin provided on the acetabular insert and which develops along a centering axis, configured to be inserted in the centering hole. The centering pin is provided with an external lateral surface that has an undulating development along the centering axis.

Abstract: The invention relates to a femoral component (1) of a knee replacement assembly. The knee replacement assembly is arranged to articulate about an articulation axis (X). The femoral component comprises an outer surface (100), wherein the outer surface is arranged to define a replacement condyle; and an inner surface (200), opposed to the outer surface, wherein the inner surface is adapted for attachment to a prepared distal femur. The inner surface comprises portions (210, 220, 230, 240) provided with mutually-parallel ridges (201) and grooves (202). The ridges and grooves are arranged to provide an increased or reduced stiffness of the femoral component when cantilevered about the articulation axis compared with a stiffness of the femoral component when cantilevered about a transverse axis.

Abstract: Disclosed is a prosthesis for a person with an amputation below the elbow to provide a replacement for at least a lower arm of the person. The prosthesis includes a receiving sleeve adapted to be attached to a stump of the person such that the stump can move the receiving sleeve. An electromechanical hand is attached to the receiving sleeve, the electromechanical hand having a rotary mechanism, a control unit, at least one finger and at least one motor. The rotary mechanism includes a potentiometer having a shaft in communication with the receiving sleeve such that a displacement of the receiving sleeve causes a corresponding rotation of the shaft of the potentiometer. The control unit is configured to measure the corresponding rotation of the shaft of the potentiometer and send a signal to the at least one motor to actuate the at least one finger.

Abstract: Various embodiments of the present invention generally relate to prosthetic partial finger designs that can mimic the last two joints of the finger. Some embodiments include a proximal phalange, a distal phalange coupled to the proximal phalange, and a knuckle track (e.g., formed in an arc). The knuckle track can be moveably coupled to the proximal phalange an may include multiple teeth formed on which the proximal phalange slides along. A ratcheting mechanism can contact the multiple teeth to allow sliding in only a first direction while the ratcheting mechanism is engaged. Some embodiments include a release mechanism (e.g., a button) configured to disengage the ratcheting mechanism from the multiple teeth to allow the distal phalange to slide in a second direction. In some embodiments, the device may include a spring-back capability that automatically extends the finger after reaching full finger flexion, enabling one-handed use.

Abstract: A method of implanting a joint prosthesis assembly for joint arthroplasty using a coupling mechanism is disclosed. The method includes exposing a joint of a patient, resecting a portion of the joint, inserting a second prosthesis of the joint prosthesis assembly into a medullary canal, and inserting a first prosthesis of the joint prosthesis assembly from a lateral side of the joint. The joint prosthesis assembly includes a magnet. The magnet is configured to lock the first prosthesis of the joint prosthesis assembly to the second prosthesis of the joint prosthesis assembly. The first prosthesis of the joint prosthesis assembly includes a recess. The second prosthesis of the joint prosthesis assembly includes a protrusion. The recess is configured to house the protrusion. Alternatively, the first prosthesis and the second prosthesis may be assembled in a direct line using the magnet for secure coupling of the components.

Abstract: An ankle prosthesis comprises a foot prosthesis. A lower ankle is pivotably secured to the foot prosthesis at an ankle joint. An upper ankle is connected to the lower ankle in a manner that permits vertical movement of the upper ankle relative to the lower ankle. A coupling spring is biased in an extended condition. The coupling spring is connected at a first end to the upper ankle. A second end of the coupling spring is movable in a first condition which is engaged to the lower ankle and in a second condition engaged to the foot prosthesis. Energy is stored in compression of the coupling spring when the coupling spring is in the first condition and energy is released from the coupling spring when the coupling spring is in the second condition.

Abstract: The present inventions relate to devices and methods that improve the positioning and fit of orthopedic reconstructive joint replacement stem implants relative to existing methods. For example, an embodiment of the device provides a stem component comprising proximal and distal body portions that can be configured to mimic a geometric shape of a central cavity region created in a bone of a joint for improving conformance and fixation of the stem component thereto. Further, another embodiment provides a system of stem implants that each have a unique medial offset for facilitating the matching of an implant to the geometry of a central cavity region of a bone. Additionally, an inclination angle of a resection surface of each of the implants in the system can remain constant or vary as a function of the medial offset.

Abstract: Embodiments of an implant assembly for reverse shoulder arthroplasty is disclosed. In one embodiment, the implant assembly comprises a humeral component and an adaptor coupled to the humeral component. The humeral component comprises a stem portion and a neck portion. The stem portion is configured for fixation to a humerus, and the neck portion is angularly oriented relative to the stem portion. The adaptor comprises a first bearing surface and a second bearing surface opposite the first bearing surface. The first bearing surface interfaces with an articulating surface of the neck portion to allow the adaptor to rotate relative to the humeral component in a plane that is generally parallel to the articulating of the neck portion. The second bearing surface is configured to interface with a glenosphere component to allow the glenosphere component to articulate relative to the adaptor.

Abstract: A surgical shoulder articulation replacement method is provided. The method can include providing a humeral implant having a hollow stem. The hollow stem can be provided with a sharp distal edge. The method can include impacting the humeral implant in a cancellous bone of a humeral head of a patient, with the sharp distal edge cutting the cancellous bone in the process.

Abstract: A multi-articulated link knee joint includes: a knee unit in which an upper link member is structured to rotate relative to a lower link member by a multi-articulated link mechanism including a plurality of link members including the upper link member and the lower link member; a driven member to move in accordance with the rotation of the upper link member; a position detector for detecting the position of the driven member, the position detector provided at the lower link member; and an angle detector for obtaining the bending angle of the knee unit from the position of the driven member.

Abstract: The present invention teaches a shock and torsion absorber that includes a base member having an accommodation space and an exhaust opening, a cushion member joined to a bottom end of the base member, a limit member including a positioning element and a seal element, and a joint member having an intake element, a trough, and a axial channel. A piston is housed in the joint member. The axial channel allows a shaft to thread through via the positioning element and to join with the shaft limit element. A bottom end of the positioning element is connected to the cushion member. The piston is connected to a top end of the positioning element. An upper vacuum chamber is formed above the seal element in the joint member. A lower vacuum chamber is formed beneath the piston and the seal element.

Abstract: A device, a kit and a method are presented for permanently augmenting the pump function of the left heart. The basis for the presented innovation is an augmentation of the physiologically up and down movement of the mitral valve during each heart cycle. By means of catheter technique, minimal surgery, or open heart surgery implants are inserted into the left ventricle, the mitral valve annulus, the left atrium and adjacent tissue in order to augment the natural up and down movement of the mitral valve and thereby increasing the left ventricular diastolic filling and the piston effect of the closed mitral valve when moving towards the apex of said heart in systole and/or away from said apex in diastole.

Abstract: Prosthetic implant devices and related methods are provided. The prosthetic implant devices include an internal component and an external component. The internal component has an implant portion associated with one or more rare earth magnets. The internal component being of a size and shape suitable for surgical implantation into the residual limb of the amputee. The one or more rare earth magnets generate at least one magnetic field. The external component having a prosthetic piston associated with a plurality of magnetic elements and a prosthetic cup associated with a magnetic array. The magnet elements of the prosthetic piston being in adaptable magnetic association with the at least one magnetic field generated by the one or more rare earth magnets.

Abstract: A prosthetic foot cover for a prosthetic foot having a sagittal plane and a plantar surface including a first cover component having a first internal cavity and being adapted to receive and cover a first portion of the prosthetic foot, a second cover component having a second internal cavity and being adapted to receive and cover a second portion of the prosthetic foot, and a means for detachably attaching the first cover component and the second cover component to the prosthetic foot. The first internal cavity has a first internal cavity contacting surface that directly contacts the first portion of the prosthetic foot, and the second internal cavity has a second internal cavity contacting surface that directly contacts the second portion of the prosthetic foot. A method for installing the prosthetic foot cover on the prosthetic foot.

Abstract: The present invention relates to an electronic artificial hand including a power section, a tendon section, and a restoring line section for joint movement of a finger group which is capable of preventing unnecessary driving of the power section using tension of the tendon section caused by the joint movement of the finger group and implementing a gripping force similar to a gripping force of a person through a physical configuration using the tension of a spring section and the tendon section and which is easily implemented due to a simplified configuration and has low manufacturing costs.

Abstract: A hydraulic system for adjusting a prosthetic limb. The hydraulic system may include an expandable pad mounted onto an interior surface of a socket of the prosthetic limb. The hydraulic system may further include a hydraulic cylinder and a plunger mechanism. The hydraulic cylinder may be filled with a hydraulic oil. The hydraulic system may be configured to expand the expandable pad by pumping the hydraulic oil from the hydraulic cylinder into the expandable pad responsive to a volume decrease of the residual limb being more than a threshold.