A stemless humeral anchor (10) includes a first end (12) configured to be embedded in a proximal portion of a humerus and a second end (14); a mating portion (16) for an articular component; a transversely extending collar (20); and a rotation control feature (22, 22A) for resisting rotation when the stemless humeral anchor is implanted. A void filling protrusion (24) can extend circumferentially from rotation control feature and can include a porous shell (26), in which a void filling component (28) can be disposed. The rotation control feature can comprise arms. One or more arms (22A) can have a larger radial extent than the others (22). A prosthesis assembly includes a base member (104) that has a helical structure (224) and one or more pathways (300). The pathway is accessible from a proximal end and is directed distally through the helical structure. The pathway is located inward of an outer periphery of the helical structure. The pathway extends in a space between successive portions of the helical structure. The prosthesis assembly includes a locking device (108) that has a support member (132) and an arm (110) that projects away from the support member. The arm is disposed in the pathway when the support member is disposed adjacent to the proximal end of the base member. The arm is disposed through bone in the space between successive portions of the helical structure when the prosthesis assembly is implanted.

A reference-point providing (RPP) device for conversion of unicompartmental knee arthroplasty (UKA) to total knee arthroplasty (TKA), has a wedge having a joint surface, a bottom flat surface, and a second surface, the second surface extending from the bottom flat surface to the joint surface at a thick end of the wedge and a mounting flange; the wedge fitting in a space remaining after removal of a UKA implant with the joint surface providing a reference point for determining alignment of a TKA implant. Converting a UKA to TKA with the RPP requires removing UKA implant from a femur of a patient, inserting the RPP and attaching it to the femur; using a posterior reference guide having a first paddle on a condyle of the femur and a second paddle on the RPP, to determine necessary alignment and rotation of the TKA implant; and removing the RPP.

A stemless humeral shoulder assembly having a base member and an anchor advanceable into the base member. The base member can include a distal end that can be embedded in bone and a proximal end that can be disposed at a bone surface. The base member can also have a plurality of spaced apart arms projecting from the proximal end to the distal end. The anchor can project circumferentially into the arms and into a space between the arms. When the anchor is advanced into the base member, the anchor can be exposed between the arms. A recess can project distally from a proximal end of the anchor to within the base member. The recess can receive a mounting member of an anatomical or reverse joint interface.

An expandable interbody device for placement between adjacent vertebrae having an upper structure, a lower structure and a screw mechanism, wherein actuation of the screw mechanism moves the upper and lower structures between a collapsed configuration and an expanded configuration. A deployment tool couples to the expandable interbody device for positioning the device between adjacent vertebrae, actuating the screw mechanism and delivering a material to a chamber of the expandable interbody device.

The present disclosure relates generally to the field of mammalian prosthetics, and more specifically to prostheses for use in total or partial joint replacement, and to a method of use of these prostheses in arthroplasty. Thus, disclosed is a prosthesis for use in hip arthroplasty that comprises an artificial femoral head that includes a head portion constructed totally or partially of a polymeric material, and a connector means designed to connect said head portion in a non-articulating manner to a femoral stem portion. The head portion may be made solely of solid polymeric material or of an outer shell of polymeric material connected in a non-articulating manner to an embedded core. The polymeric material is preferably selected from ultra-high molecular weight polyethylene (UHMWPE) or radiation treated UHMWPE having substantially no detectable free radicals. The embedded core comprises, for example, one or more of solid non-polymeric material (e.g., metallic, ceramic, or ceramic-on-metal material), a multiplicity of metallic spokes, a metallic scaffolding, and/or combinations thereof.

A stemless humeral shoulder assembly having a base member and an anchor advanceable into the base member. The base member can include a distal end that can be embedded in bone and a proximal end that can be disposed at a bone surface. The base member can also have a plurality of spaced apart arms projecting from the proximal end to the distal end. The anchor can project circumferentially into the arms and into a space between the arms. When the anchor is advanced into the base member, the anchor can be exposed between the arms. A recess can project distally from a proximal end of the anchor to within the base member. The recess can receive a mounting member of an anatomical or reverse joint interface.

A prosthesis may include a first component, a second component, and a coupling member. The first component may include a first body extending from a first end to a second end, which may define a first opening that extends inwardly toward the first end. The first opening may include a first portion having a first diameter and a second portion having a second diameter. The second component may include a second body extending from a first end to a second end. The second body may define a second opening that extends through the second body. The coupling member may be configured to couple the first component and the second component by compressing the first component and the second component. The coupling member may include a shaft portion and a head portion. The shaft portion may be sized and configured to be received in the first opening and the second opening.

An expandable interbody device for placement between adjacent vertebrae having an upper structure, a lower structure and a screw mechanism, wherein actuation of the screw mechanism moves the upper and lower structures between a collapsed configuration and an expanded configuration. A deployment tool couples to the expandable interbody device for positioning the device between adjacent vertebrae, actuating the screw mechanism and delivering a material to a chamber of the expandable interbody device.

Methods of additive manufacturing expandable medical implants is provided along with methods of patient imaging for 3D printing expandable spine cages and topographically matching patient specific implants. Methods for stabilizing and correcting the alignment of the spine are also provided. Spine pathologies such as lordosis, kyphosis and scoliosis can be corrected with properly expanding spine cages such as those described. Independent control and adjustment of the proximal and distal ends of spine cages allows for treating multiple horizontally affected intervertebral spaces.

The invention relates to an attachment member (2) and a connecting member (16) for a carpometacarpal thumb joint prosthesis (1) as well as to said thumb joint prosthesis. The attachment member (2) comprises a screw-like part (4) for attachment by screwing into the second metacarpal bone and a locking device (8) for locking the screw-like part to the connecting member (16). The connecting member comprises an elongated, arcuate element (16) which at one end portion (16a) thereof is configured with a hole (14) for connection to the attachment member (2) for the second metacarpal bone and which at the opposite end portion (16b) thereof is configured with a hole (15) for connection to an attachment member (3) for the first metacarpal bone. The joint prosthesis (1) comprises said attachment member (2) for the second metacarpal bone, an attachment member (3) with a screw-like part (5) for attachment by screwing into the first metacarpal bone and with an articulating ball element (6) as well as a corresponding articulating socket element (7), and said connecting member (16).