The invention relates to a modular humeral prosthesis for an inverse shoulder prosthesis, comprising an anatomical shaft (1) and a separable epiphyseal head (2) which may be angularly orientated by rotation about the longitudinal axis (XX) of the anatomical shaft. The anatomical shaft and the epiphyseal head comprise complementary angular indexing means (11, 28) for relative rotational fixation.

A prosthesis system comprises plates that can be positioned against vertebrae and a selected resilient core that can be positioned between the plates to allow the plates to articulate. The selected resilient core can be chosen from a plurality of cores in response to patient characteristics, such as age and/or intervertebral mobility, such that the prosthesis implanted in the patient is tailored to the needs of the patient. The plurality of cores may comprise cores with different resiliencies, and one of the cores can be selected such that the upper and lower plates articulate with the desired shock absorbing resiliency and/or maximum angle of inclination when the one selected core is positioned between the plates.

A glenoid component in one embodiment includes a base component with a planar upper circular rim defining a first plane, a receptacle opening to the first plane, and a lower planar circular surface defining a second plane parallel to the first plane. An articulating component of the glenoid component includes an upper articulating surface, a lower cylindrical coupling portion configured to be inserted into the receptacle, and an overhang portion located above the lower cylindrical coupling portion and beneath the upper articulating surface. The overhang portion includes a planar lower surface extending outwardly from the lower cylindrical coupling portion and configured to abut the planar upper circular rim of the base component when the articulating component is coupled to the base component.

A trial medical instrument for aligning an acetabular component, comprising: a first portion configured to fit within a patient's acetabulum; and a second portion extending from the first portion; wherein the second portion extends from the first portion in a direction that mimics a shape formed by a femoral implant component coupled with an acetabular implant component when a femur to which the femoral implant component is coupled is in a position relative to an acetabulum to which the acetabular implant component is coupled that is near an extent of a typical range of motion of the femur. As used herein, the phrase “extent of a typical range of motion” describes typical angular displacements of a femur as usually limited by patient anatomy.

Methods and devices are disclosed for joint (e.g., shoulder) arthroplasty. In one aspect, there is provided a device for determining inclination and/or version of a prosthetic head with respect to a prosthetic stem. In another aspect, there is provided a joint (e.g., shoulder) prosthesis. In another aspect, there is provided a method for setting an inclination angle and/or a version angle of a prosthetic head with respect to a stem implanted or to be implanted in a bone of a joint (e.g., shoulder).

An implant trial includes a trial body and an indicium disposed in the trial body. The trial body is positionable in a subject. The indicium is designed and constructed to indicate a parameter of the implant trial. The indicium is radiographically visible when the trial body is positioned in the subject. The implant trial may be a trial spacer for vertebrae.

A system for aligning components of a prosthetic includes a mounting plate, a fastener and an adapter coupling plate. The mounting plate comprises: a first major surface; a second major surface opposing the first major surface; an adapter accommodation hole extending through the mounting plate; and sizing indicia located on the second major surface. The fastener extends from the mounting plate. The adapter coupling plate comprises: a third major surface; a fourth major surface opposing the third major surface; an adapter coupling hole extending through the adapter coupling plate and surrounded by the adapter accommodation hole; and an indicator located on the fourth major surface to point to the sizing indicia on the mounting plate. The adapter coupling plate can be slidable along a slot surrounding the fastener or a tongue and groove system connecting the adapter coupling plate and the mounting plate and locked via the fastener.

This disclosure relates to a graft preparation station and methods for repairing bone defects. The station described herein may be utilized for dimensioning a graft prior to positioning the shaped graft at a surgical site.

Apparatuses, systems and methods such as a trial apparatus for selecting a position of a prosthetic head component on a humerus are disclosed. The trial apparatus can optionally include a body (36) and a thimble (38). The body can have a plurality of indicia (46) and can form a portion of a joint (37). The thimble can be couplable to the body via the joint. The thimble can be rotatable relative to the body via the joint and can include one or more indicia (62) for use with the plurality of indicia of the body. The thimble can be mountable to a prosthetic stem (30) implanted in the humerus.

A system configured to increase height of a vertebral body. An implant includes plates each defining a bearing surface configured to be moved away from one another to expand the implant within the vertebral body. Supports are each coupled to one of the plates and include a reduced thickness portion defining a material web configured to plastically deform during expansion of the implant. The system includes an implant carrier with which an end element of the implant is removably coupled, and a rod configured to be translated relative to the implant carrier to cause expansion of the implant. An opposed portion may be coupled to the supports and configured to receive a longitudinal force to be moved relative to the end element. Second supports may be each coupled to the end element and one of the plates. Each of the second supports may plastically deform during expansion of the implant.