A surgical component, a kit including the surgical component, and a surgical method. The surgical component includes a body portion. The surgical component also includes an elongate stem for inserting into an intramedullary canal of a patient. The elongate stem extends distally from the body portion. The elongate stem has a longitudinal axis; a proximal end; a distal end; and a plurality of splines located on an outer surface of the stem. The splines are circumferentially arranged around the stem. At least some of the splines are tapered such that each tapered spline is narrower at a distal part of that spline than at a part of that spline that is proximal with respect to the distal part. The surgical component further includes an elongate neck portion extending from the body portion at a non-zero angle with respect to the longitudinal axis of the stem.

Disclosed is a prosthetic joint assembly for joining a humerus bone to a scapula bone, comprising a humeral component adapted for engagement with said humerus bone and a concave dish; a scapular component adapted for engagement with said scapula bone and a convex surface adapted to engage said concave dish; wherein when said components are implanted and engaged in a rest position said prosthetic center of rotation is displaced in a direction that is inferior and medial relative to a natural center of rotation and said humerus bone is displaced in a direction that is inferior relative to said natural center of rotation.

The present disclosure provides an orthopedic implant that can include an intramedullary stem transition region that fits in the bony intramedullary canal. The transition region can run as a monolithic piece between the implant body and the intramedullary stem, with a squared cross-section away from the implant body and a circular cross-section close to the stem body. The transition region can allow for higher implant strength with reduced rotation for the implant.

A surgical procedure method includes accessing an implanted joint prosthesis having an implant engaged within a bone of the joint and a first articulating component mounted by a first mating component to a first insert component removably mounted to the implant, and partially disassembling the accessed implanted joint prosthesis by removing the first insert component with the first articulating component fixed thereto from the implant while the implant is engaged with the bone. The angular position of the first mating component with respect to the first insert component is then determined and replicated with a second insert component and a second mating component. The second insert component and the second mating component are then fixed at the replicated angle and the fixed second insert component and second mating component are mounted to the implant engaged within the bone. A new articulating component is then mounted to the second mating component.

A bone press includes a base; a compression plate located opposite to the base; a housing that extends between the base and the compression plate, the housing extending along a longitudinal axis of the bone press; a pressing zone within the housing and between the base and the compression plate along the longitudinal axis of the bone press; and an actuator to provide relative movement between the compression plate and the base to create compression in the pressing zone.

The invention relates to a method for surgical application of a glenoid anchor of a shoulder joint prosthesis and instruments advantageously used in the method. The method includes making a delto-pectoral incision providing a delto-pectoral access to a shoulder joint; with the delto-pectoral access being suitable for inserting at least one machining tool; and making a trans-deltoid incision providing a trans-deltoid access to the humeral head; with the trans-deltoid access being suitable for inserting a stem of a machining instrument to be mounted on the machining tool for machining the glenoid cavity.

A stemless implant for shoulder arthroplasty includes a body having a proximal portion, distal portion, and an outer surface. A cylindrical extrusion is substantially perpendicular to and adjacent the proximal portion. At least a portion of the outer surface is configured to contact bone, the outer bone contacting surface comprising a concave taper. The stemless implant can be sized and shaped for insertion into a metaphysis of a humerus bone without penetrating a diaphysis of the humerus bone. The implant optionally comprises a medial fin, a lateral fin, an anterior fin, and a posterior fin. The medial fin and lateral fin may be thicker than the anterior fin. The fins may taper from the proximal portion to the distal portion.

A bone void forming assembly includes a support member having a head portion and an elongate portion extending therefrom. A guide member is connected to the support member and has a guide body including a channel extending therethrough. The channel defines an axis offset and obliquely angled relative to an axis of the elongate portion. The assembly also includes reamer having a cutting head and a stop member. A bushing is slidably connected to the reamer between the stop member and cutting head and is slidably connectable to the guide body via the channel.

The invention concerns a method for manufacturing a prosthesis (11) for a fractured long bone of a patient, the method comprising the steps of: A) providing data representative of the fractured long bone, the fractured long bone comprising a diaphyseal fragment (2) comprising a medullary cavity (8); B) based on said data, designing the prosthesis specifically to the patient, the prosthesis comprising a stem part (12) configured to be inserted into the medullary cavity, step B) comprising: a sub-step of choosing, specifically to the patient, a contact zone (40) of the medullary cavity onto which a respective chosen mechanical stress is planned to be applied by the stem part, and a sub-step of designing the stem part so that the stem part may be inserted into the medullary cavity and thus apply the chosen mechanical stress to said contact zone; and C) manufacturing the prosthesis designed at step B).

A humeral prosthetic head has a non-spherical articulation surface coupled with an intermediate component connecting the head and the humerus, the intermediate component connected to the epiphysis, metaphysis, or diaphysis, or to one or more additional components connected to the humerus. The intermediate portion provides for axial and angular offset of the head with respect to a connection to the humerus, using a curvilinear tapered engagement.