This shoulder prosthesis glenoid component (2) has on one of its faces an articulation surface (S.sub.A) adapted to cooperate with a humeral head and having, on an opposite face (S.sub.G) adapted to be immobilized on the glenoid cavity (G) of a shoulder, a keel (4) for anchoring it in the glenoid cavity (G). This keel (4) comprises a body (5) that extends from the opposite face (S.sub.G). The keel (4) comprises at least one fin (6) projecting from the body (5) 2 which runs over at least a part of the perimeter of the body (5).

A surgical pelvic drill for operating hip osteoarthritis adapted to create a hole in the pelvic bone of a human patient is provided. The pelvic drill is adapted to create a through-going hole placed in the acetabulum area from the abdominal side of the pelvic bone of the human patient. The pelvic drill comprises: a driving member, a bone contacting organ in connection with said driving member, an operating device adapted to operate said driving member. The bone contacting organ is adapted to create a hole in the acetabulum area starting from the abdominal side of the pelvic bone through repetitive or continuous movement. A surgical and a laparoscopic/arthroscopic method of using said pelvic drill is further provided.

The present disclosure provides an artificial alpha femoral stem prosthesis which includes a femoral stem cone, a femoral neck and a stem body connected integratedly, wherein a tool operating hole is arranged at upper end of the the femoral neck; the stem body comprises a proximal segment of the femoral stem, a middle segment of the femoral stem and a distal segment of the femoral stem, and there is a deflection angle between the femoral neck and the stem body.

The present disclosure provides a cobra type femoral stem prosthesis, that is a femoral stem prosthesis for congenital dysplasia of the hip (CDH) which includes a femoral stem cone, a femoral neck and a stem body which are connected sequentially; the stem body includes proximal segment of femoral stem, middle segment of femoral stem and distal segment of femoral stem, wherein the femoral stem cone is a cone shape; One end of the femoral neck is connected with the proximal segment of femoral stem and there is a deflection angle therebetween and the other end of the femoral neck is connected with the large diameter end of the femoral stem cone.

The invention relates to an assembled vertebral body used in a cervical reconstruction operation, comprising: an upper connecting element, an artificial vertebral body element and a lower connecting element, wherein the upper connecting element is disposed at an upper part of the artificial vertebral body element, the lower connecting element is disposed at an lower part of the artificial vertebral body element, and wherein the artificial vertebral body element is assembled with the upper connecting element and the lower connecting element, respectively. The invention has the advantages that the artificial vertebral body element is customized in accordance with the characteristics of patients and printed in 3D, and the length of the artificial vertebral body element can be precisely adjusted to adapt to the patient. Since the lower connecting element is standard part, the upper connecting element is standard part or non-standard part, and the artificial vertebral body element is non-standard part, in comparison to the traditional 3D printing which needs to be printed integrally, the adjustable assembled artificial vertebral body can reduce 3D printing materials and reduce the cost of 3D printing, thus reducing medical costs for the patient. The shape of the nested parts of the elements is a non-circular shape, which can resist rotation, so that no relative movement occurs among the three elements of the artificial vertebral body.

The present invention relates generally to a prosthetic spinal disc for replacing a damaged disc between two vertebrae of a spine. The present invention also relates to a method for implanting a prosthetic spinal disc via anterior or anterior lateral implantation. Other surgical approaches for implanting the prosthetic disc may also be used.

The prosthetic joint has at least two members having each a cooperating articulating surface layer on a substrate material. At least one of said articulating surface layers comprises amorphous diamond-like carbon; or Titanium Nitrate (TiN) on a bonding layer bonded to the substrate material. The prosthetic joint provides a reduction of the number of wear debris and shows enhanced dry run properties.

An artificial replacement disc includes a pair of substantially parallel plates formed to occupy a space defined by vertebral endplates, each of the plates including a plurality of spikes on a first surface and a concave trough formed on a second surface opposite of the first surface. A mobile core includes a core rim with opposing convex surfaces extending from opposite sides of the core rim, the mobile core being capable of being disposed between the pair of plates to permit the vertebral endplates to move relative to one another. The spikes on each of the plates extend substantially away from the mobile core and the convex surfaces are formed to integrally fit within the concave trough of at least one of the plates. The core rim limits lateral movement of the mobile core relative to the parallel plates. One or more insertion tools for inserting and implanting the replacement disc are also 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 hip implant has a neck body that connects to a bone fixation body. The bone fixation body has a porous structure with an elongated shape. An internal cavity is formed in the bone fixation body and includes a substance to stimulate bone growth.