The present disclosure includes, in one embodiment, a talar component of an ankle joint prosthesis for engagement with a talus bone having a medial side wall and a lateral side wall, opposite the medial side wall, each side wall terminating at a distal edge, and the distal edges adapted to drive into the talus bone. When implanted, the side walls may form a seal between the talus bone and the component to prevent fluid from flowing under the component.

A kit for installation of prosthetic components and/or biomedical implants includes a prosthetic component having an intraosseous taproot, formed of one piece with the prosthesis, for the attachment of the prosthetic component to the bone of a patient. The prosthetic component and the taproot are made of a biocompatible metal material, and the taproot has at least one portion with a triangular cross-section, as viewed in a horizontal cross-sectional plane. At least one first guiding component for a guide wire, for guiding the insertion of a guide wire into the bone, and at least one second guiding component for an impactor having a triangular section are also included.

In an artificial knee joint implant, an increase in constraint force of a femur component and a tibia component in the anterior-posterior direction and the left-right direction of a patient is enabled, and an increase in an allowable degree of medial pivot motion is enabled. An artificial knee joint implant has a femur component to be fixed to a distal portion of a femur of a patient, and a tibia component to be fixed to a proximal portion of a tibia of the patient. Femur sliding faces of the femur component and tibia sliding faces of the tibia component each include a region in which the curvature radius varies in a predetermined direction.

Shoulder arthroplasty systems and configurations for components thereof are described. For example, implant systems for a total should arthroplasty (TSA), hemi shoulder arthroplasty, and reverse should arthroplasty (RSA) are described. In addition, exemplary configurations for baseplates, glenoid components, glenosphere components, humeral components, humeral head components, humerosocket components, connectors, and adaptors, are described.

Shoulder arthroplasty systems and configurations for components thereof are described. For example, implant systems for a total should arthroplasty (TSA), hemi shoulder arthroplasty, and reverse should arthroplasty (RSA) are described. In addition, exemplary configurations for baseplates, glenoid components, glenosphere components, humeral components, humeral head components, humerosocket components, connectors, and adaptors, are described.

A method for reducing prosthetic loading failure including the steps of providing a prosthesis for a vertebral column comprising at least an upper part for attachment to an upper vertebrae and a lower part for attachment to a lower vertebrae, the upper part having a lower curved surface and the lower part having an upper curved surface, wherein the upper and lower curved surfaces have a center of radius of curvature offset rearwardly with respect to a central vertical axis through the upper and lower vertebrae, and positioning the centroid of at least one of the upper and lower parts substantially on the same vertical axis of the center of radius of curvature.

A temporomandibular joint replacement system includes a condylar component secured with a mandibular bone and a fossa component with a fossa backing secured with a zygomatic bone and slidably attached with a removable fossa lining, the fossa lining having an open-ended concave fossa dome with a post-center peak to allow for mediolateral and anterior translation with a rounded, oblong condylar head of the condylar component. The slidable attachment mechanism of the fossa backing and fossa lining is laterally-oriented to allow for post-implantation removal and replacement without disturbing any bone or bone-interfacing components. The bone-interfacing surfaces are anatomically-contoured to their respective bone surfaces and formed with materials and textures which promote osseointegration with the joint replacement.

The present invention relates to devices and methods for treating one or more damaged, diseased, or traumatized portions of the spine, including intervertebral discs, to reduce or eliminate associated back pain. In one or more embodiments, the present invention relates to an expandable interbody spacer. The expandable interbody spacer may comprise a first jointed arm comprising a plurality of links pivotally coupled end to end. The expandable interbody spacer further may comprise a second jointed arm comprising a plurality of links pivotally coupled end to end. The first jointed arm and the second jointed arm may be interconnected at a proximal end of the expandable interbody spacer. The first jointed arm and the second jointed arm may be interconnected at a distal end of the expandable interbody spacer. The first jointed arm and the second jointed arm may each be configured to fold inward in opposite directions to place the expandable interbody spacer in an expanded position.

Shoulder arthroplasty systems and configurations for components thereof are described. For example, implant systems for a total should arthroplasty (TSA), hemi shoulder arthroplasty, and reverse should arthroplasty (RSA) are described. In addition, exemplary configurations for baseplates, glenoid components, glenosphere components, humeral components, humeral head components, humerosocket components, connectors, and adaptors, are described.

Implant includes a body and a utile feature, for example, a smooth articulating surface. A transverse rail stem system with a plurality of rails is provided, spaced apart from the utile feature, which is adapted for transverse insertion into a bodily substrate, for example, resected bone. A surgical templatefor example, to assist in sawing, drilling with a drill bit and drill guide, and broaching with a broachalong with such bone removal tools can help prepare the bone for receipt of the implant.