Systems, devices, and methods are provided for orthopedic implants. The implants may include a base member, such as an acetabular shell or an augment, that is configured to couple with an augment, flange cup, mounting member, or any other suitable orthopedic attachment. Mounting members include, for example, flanges, blades, hooks, and plates. In some embodiments, the orthopedic attachments may be adjustably positionable about the base member or other attachments, thereby providing modularity for assembling and implanting the device, and various securing and/or locking mechanisms may be used between the components of the implant.

A prosthetic shoulder implant system includes a prosthetic humeral implant and a version device. The humeral implant includes a catch member aperture and a first locking pin aperture. The version device includes a rotatable member with a body and a flexure member, and a plate with a catch member and a projection contacting the flexure member. A first locking pin extends from the version device and is adapted to mate with the first locking pin aperture. In an unlocked condition of the system, the rotatable member has a first rotated position in which the flexure member is in an uncompressed state and the plate is in a first position, and in a locked condition of the system, the rotatable member has a second rotated position in which the flexure member is in a compressed state and the plate is in a second position proximal of the first position.

Systems, devices, and methods are provided for orthopedic implants. The implants may include a base member, such as an acetabular shell or an augment, that is configured to couple with an augment, flange cup, mounting member, or any other suitable orthopedic attachment.

An apparatus and method for aligning an acetabular cup. The apparatus may include an acetabular cup (150, 10) and/or a protractor (30) and/or a depth gauge tool (90) and may be provided in the form of a surgical kit. Components of the apparatus may allow an angle of rotation of an acetabular cup about an axis (111) of the cup relative to an anatomical feature of a patient to be determined when the acetabular cup implant is placed in the acetabulum of the patient. Components of the apparatus may allow an amount of overhang between a rim (12, 162) of an acetabular cup and an edge of the acetabulum to be determined. The acetabular cup may be an acetabular trial cup (10) or and acetabular cup implant (150). Embodiments of the invention may allow both the angle of rotation about the cup axis and the amount of overhang between the rim and the acetabulum edge to be determined.

A humeral head assembly is provided that includes an articular body and a coupler. The articular body includes a coupling portion disposed on a side of the articular body opposite an articular surface. The coupling portion includes a continuous zone of eccentricity adjustment. The coupler portion optionally includes one or more than one discrete position site. The coupler includes a first portion and a second portion opposite the first portion. The first portion is configured to mate with the coupling portion and the second portion is configured to mate with another member of a joint prosthesis. A coupling portion with the continuous range of eccentricity adjustment can be provided on a bone anchor and the eccentricity of another component can be selected by motion of a coupler, such as a tray for reverse humeral assemblies, along the coupling portion of the anchor.

An implant resection system for preparing an implant site to replace a defect in an articular surface of a first bone includes a first guide configured to be coupled generally to the first bone. The first guide includes a body portion defining a channel configured to receive a pin, wherein the pin is configured to penetrate and form a longitudinally disposed bore within the first bone. The implant resection system further includes a second guide configured to be coupled generally perpendicular to the first bone proximate to the defect by way of the bore. The second guide includes a drill bit configured to form an excision site through a portion of the articular surface in preparation of receipt of an implant.

An expandable interbody spacer for the spine is provided. The spacer includes upper and lower endplates simultaneously movable with respect to a housing along an axis traverse to a longitudinal axis to increase or decrease the height of the spacer selectably along both an anterior side and a posterior side for uniform expansion/contraction of the endplates or only along the anterior side for angular expansion/contraction of the endplates. A spacer deployment instrument is provided that is selectable to effect uniform or angular expansion/contraction. When uniform expansion/contraction is selected a gear on an anterior rod is engaged with a gear on a posterior rod to simultaneously rotate both rods in opposite directions. Opposite threads on actuators of the spacer effect translation of the actuators in the same direction along the longitudinal axis.

The biocompatible lattice structures disclosed herein with an increased or optimized lucency are prepared according to multiple methods of design disclosed herein. The methods allow for the design of a metallic material with sufficient strength for use in an implant and that remains radiolucent for x-ray imaging.

Apparatus and Method for Hip Surgery. An adjustable trial femoral head (400) for assessing anteversion of an acetabular cup relative to a pelvis of a patient are described. The adjustable trial femoral head comprises a spherical body (402) having a bore extending along a polar axis of the spherical body and configured to receive a free end of a femoral neck. A visual alignment guide (420) is mounted on the at least partially spherical body and the orientation of the visual alignment guide relative to the spherical body is adjustable.

A femoral component kit includes a piston. The piston includes a notch formed in a bottom surface. The kit includes a femoral component mold having a mold body with a first sidewall, a second sidewall, and a bottom. The sidewalls and bottom define a recess for receiving an antibiotic-impregnated material. The recess includes depressed sections that are spaced apart by an inner section. The outer sections are transverse to a longitudinal axis of the mold. The inner section includes a keel that extends upward and has a height that sets a size of a femoral component produced using the mold. The keel is aligned with the notch when the piston is inserted within the mold. The notch and the keel may include one or more calibration markings that indicate increments of adjustments to the size of the femoral component and resulting flexion and extension gaps and joint space position.