An interbody spinal cage comprising: a body portion comprising a superior side, an inferior side and at least one lateral side connecting the superior side and the inferior side; and at least one endplate portion coupled to the superior side or the inferior side of the body portion, the at least one endplate portion comprising a unibody structure and operable to be fixedly coupled to an anatomical structure of a patient and decoupled from the superior side or the inferior side of the body portion.

Thoracic/lumbar and cervical spinous process staples which staple/fuse adjacent spinous processes are disclosed. Thoracic/lumbar transverse process staples which staple/fuse adjacent transverse processes are also disclosed. Each embodiment has upper and lower claws connected by a ratchet spring mechanism, along with a multiplicity of bone fastener prongs attached to the upper and lower claws. Two sets of prongs on each staple claw are spaced by a distance approximately equal to the distance separating adjacent spinous or transverse processes so as to facilitate stapling/fusion of two adjacent processes. Also disclosed are staple prongs with multiple perforations which enable incorporation of bone fusion material thereby facilitating stapling/fusion of spinal elements.

An implant is disclosed that has a base member, an articulating member, and a coupling portion that secures the base member to the articulating member. The implant can be a shoulder implant (100, 200, 300) that has a baseplate (102, 230, 310), an articulating component (104, 210), and a fixation component (106, 270, 342). The baseplate includes a first side (110, 234, 314) with a projection (108, 240, 320) that has a first Morse taper and may be offset from a center line of the baseplate and a second side (116, 236, 316) that has a post or stem (114, 250, 330) that is offset from the center line of the baseplate. The articulating component includes a cavity (122, 220) with a second Morse taper that is offset from a center line of the articulating component. The articulating component is attachable to the baseplate when the projection is received in the cavity of the articulation component. A threaded through hole (130, 222) extends from the cavity of the articulating component to a second, convex side or articulating surface (120, 212) thereof. The through hole can be aligned with the cavity. The fixation component (106, 270, 342) can engage the through hole and is contained within a cavity (132, 322, 242) of the baseplate by a spring (138, 262, 360) and a cap (140), a second fixation member (280), or an engagement member (370).

Provided is a novel joint replacement prosthesis that includes a base component, and one or more modular stems. The base component includes a bone-facing surface including one or more stem connectors configured for receiving and forming connections with the one or more modular stems inserted from the bone-facing surface side.

A surgical tool for separating two components, for example removing a femoral head from a femoral stem, having a four bar chain whose four bars are a first handle (L1), an crossover component (L2), a second handle (L3) and a crossbar (L4) pivotally connected respectively by: a first joint (J1) between the first handle and the crossover component; a second, crossover joint (J2) between the crossover component and the second handle; a third joint (J3) between the second handle and the crossbar, and a fourth joint (J4) between the crossbar and the first handle, and wherein, upon application of a gripping force to the first and second handles, the first and second jaws separate from one another so as to separate the two components engaged therewith.

An implant is disclosed that a base member configured to be secured in bone, the base member includes a plate portion, an articulating member, and a coupling portion for securing the base member to the articulating member. A stem extends from the plate portion, where the stem is positioned offset from a center of the plate portion. The coupling portion includes a first fixation component, and a second fixation component including an opening for receiving the first fixation component, where the first fixation component is coupled to the articulating member and the second fixation component is coupled to the base member.

A system for converting a first joint prosthesis to a second joint prosthesis in-situ includes a plurality of inserts having a bone interface side and a component facing side and a plurality of articulating components having a cavity configured to receive at least one of the plurality of inserts. The plurality of inserts may be unicompartmental, bicompartmental, or tricompartmental. The inserts may be made of metal and may have a bone contacting surface made of a porous metal. The plurality of articulating components may be unicompartmental, bicompartmental, or tricompartmental. The articulating components may be sized and shaped to cover one or more of the plurality of bone interface components and span a distance therebetween. The articulating components may be made of a polymer.

A method for removing a stem portion of an orthopedic implant from a bone comprises exposing an implanted orthopedic implant having a body portion, a stem portion interconnected to the body and a porous metal section forming an interconnection between the body and the stem portion. A cutting tool is mounted on a holder connected to an exposed surface of the orthopedic implant. The porous section is aligned with the cutting tool mounted on the holder. The entire porous section is cut by moving the cutting tool therethrough in a direction transverse to the stem portion axis. The implant body portion is then removed and then the stem portion is removed from the bone. The cutting tool may be a saw or chisel which may be mounted on a guide fixed to the body portion.

A veterinary hip resurfacing prosthetic system includes a femoral cap and an acetabular cup. The cup shell has a thickness of less than 2 mm and a liner in the shell has a thickness of less than 2.5 mm in order to accommodate a larger femoral cap. Further included are features for preventing rotation of the liner relative to the shell, for releasably locking the liner in the shell, and for accessing the liner to remove it from the shell.