An artificial hip joint stem is used to replace the damaged femoral head or acetabulum and includes a stem body having a head fixing part, which fixes a head, and an operating space horizontally opened at the upper side thereof. A head insertion hole connects to the operating space. A screw part is inserted into the head insertion hole. An operation converting part is inserted into the operating space to vertically move by the screw part when the operation converting part is connected to the screw part. A fixing bracket is inserted into the operating space such that the screw part is fixed to rotate without changing the depth thereof. A variable operating part is inserted into a supporting surface of the stem body to adjust a horizontal width by means of the operation converting part. A movable pin fixes the variable operating part to the operation converting part.

A trial implant system and method of trialling are described. The trial implant system comprises a stem component having a neck including a free end and a neck longitudinal axis. A first trial head has an articulating surface and includes a bore having a bore longitudinal axis and which can receive the free end of the neck with the neck longitudinal axis and bore longitudinal axis coincident. The system includes a first formation and a plurality of second formations angularly disposed around the longitudinal axis. One of the first formation and the plurality of second formations is provided on the neck and the other is provided within the bore. Each of the second formations can matingly engage with the first formation to limit the depth of insertion of the neck into the bore by a different amount.

A modular trial implant system includes a first trial implant part that releasably connects to a second trial implant part and/or an implant part to form a first trial joint implant part. The first trial implant part has a cone receptacle for accommodating a connecting cone of the second trial implant part or the implant part. The first trial implant part includes first latching elements and second latching elements that are axially offset in the cone receptacle for latchingly engaging behind connecting cones of second trial implant parts or implant parts. The first trial implant part has a receiving sleeve defining the cone receptacle. The receiving sleeve has a wall that surrounds the implant longitudinal axis and delimits the cone receptacle. The wall is indentation-free and/or perforation-free in a first region between the first latching elements and in a second region between the second latching elements.

An antibiotic delivery system including an intramedullary stem that is adapted to be removably mounted into a medullary canal of a bone. The stem includes a body having an inlet adapted to be in fluid communication with a source of liquid-borne antibiotic and a plurality of outlets disposed along the stem. A channel extends between the inlet and the plurality of outlets for delivering a fluid-borne antibiotic from the inlet to the plurality of outlets so as to distribute the antibiotic along the medullary canal in a controlled fashion. A method of treating an infected joint during a two-stage re-implantation of an orthopedic implant is also disclosed.

An orthopedic implant in the form of a hip joint endoprosthesis consists of a head, which is set onto an anchoring shaft, which itself is insertable into a bone and anchorable therein. The head comprises an inner blind-hole-type recess, and the anchoring shaft is provided with a tenon for inserting into this recess. A sleeve provided with an approximately central through-bore is soldered into the recess of the head, via which sleeve the head is setable or mountable on the tenon. The head consists of a ceramic based on zirconium dioxide, aluminum oxide or a mixed ceramic, while the sleeve consists of a high strength titanium material. The connection between the head and the sleeve is produced by a silicate ceramic solder that solidifies or hardens in a ceramic firing, as well as by a subsequently applied glass solder, of which the excess can exit via the through-bore into a hollow space existing between the sleeve and the tenon. Both the recess of the head as well as the metallic sleeve are embodied approximately cylinder-shaped.

A prosthetic hip joint is disclosed. The prosthetic hip joint includes a femoral component, which further includes a femoral head with a femoral head cavity and an acetabular component. The acetabular component includes an acetabular cup and an acetabular cup insert. The acetabular cup insert and the acetabular cup each has a through hole, where the through holes overlap a location of a native femoral head ligament.

An apparatus for the treatment of canine or other animal hip pathologies, the apparatus (200) comprising a buffer (210) adapted to be disposed between a femur (10) and a hip socket (25), and a fixing means (250) adapted to fix the buffer to the femur.

A method of assembling a mobile bearing acetabular component of a prosthetic hip joint is disclosed. The method includes mounting an acetabular cup insert to an acetabular cup. The method includes concurrently repositioning the acetabular cup insert deeper into an interior of the acetabular cup and repositioning the acetabular cup insert outside of an outline of the acetabular cup.

An apparatus for the treatment of canine or other animal hip pathologies, the apparatus comprising a buffer adapted to be disposed between a femur and a hip socket, and a fixing means adapted to fix the buffer to the femur.

An orthopedic system for delivery of a therapeutic agent to a bone includes an elongate stem adapted to be inserted into an intramedullary canal, an inlet configured to receive the therapeutic agent, and one or more outlets configured to deliver the therapeutic agent to the bone. The elongate stem may comprise one or more protrusions to engage the bone, and one or more channels extending longitudinally therein, fluidly coupled to the inlet. The therapeutic agent flows from the inlet through the one or more channels and exits into the intramedullary canal through the one or more outlets. The system may be configured to allow one or more dimensions of the system to be adjusted to accommodate the anatomy of a patient.