Abstract: A tibial spacer paddle comprises a spacer block comprising opposing bearing surfaces, an alignment slot extending into the spacer block; and a handle extending from the spacer block. The spacer block can include feet for passively engaging the femur or pegs for actively engaging a femoral component so that the spacer block is linked to the femur while the tibia rotates. A tibial spacer system comprises a provisional component having an alignment tab extending from a body and an alignment indicator located on the body, a femoral component and a pin extending from the femoral component. The pin can engage the alignment tab so that the provisional component is linked to the femur while the tibia rotates. In addition to or alternatively to the alignment tab and pin, the provisional component can include a tibial plate that can be rotationally connected to the provisional component.

Abstract: External fixation systems, and methods for immobilizing joints or fractured bones. An external fixation system may include one or more clamp assemblies connected to one or more rod assemblies at polyaxial joints. Each rod assembly may be length adjustable, and may include a one-way locking mechanism to provisionally lock the length of the rod assembly, and additional locking mechanisms to permanently lock the length of the rod assembly. The system may be deployed pre-assembled as a unit to immobilize a joint or fracture. Another external fixation system further includes a spanning member extending transverse to the rod assemblies. Two or more external fixation systems may be deployed in a stacked configuration on one set of bone pins to immobilize two joints and/or fractures. The systems may be provided in kits including guiding instrumentation, bone pins and pin clamping assemblies for connecting the bone pins to the external fixation systems.

Abstract: Disclosed is a wedge for use during a reverse shoulder arthroplasty. The wedge can comprise a body having a proximal surface and a distal surface. The proximal surface and the distal surface can each extend from a distal end of the body to a proximal end of the body. The distal end can have a distal length and the proximal end can have a proximal length. The distal length can be shorter than the proximal length. The proximal surface can have a proximal curvature and the distal surface can have a distal curvature. The proximal curvature or the distal curvature can approximate a curvature of a deltoid muscle.

Abstract: An orthopaedic knee prosthesis includes a tibial bearing component with articular features which operate to protect adjacent soft tissues of the natural knee, promote and/or accommodate desired articulation with an abutting femoral component, and facilitate expedient and effective implantation by a surgeon.

Abstract: A femoral augment, or set of augments, for use with a knee joint prosthesis, where the femoral augment includes a main body portion, an aperture formed within the main body portion and extending in a generally distal/proximal direction, and a pair of legs extending outwardly from said main body portion in a generally posterior direction. In the preferred embodiment, the aperture is configured to receive a stem extension implant, and to allow it to pass through. Additionally, the legs of the femoral augment are preferably configured to be seated proximal of a proximal side of a pair of condylar portions of a femoral component of a knee joint prosthesis. The present invention is intended for situations in which the distal portion of the femur is defective, and it provides a method and devices that allow for preservation of healthy peripheral bone, while still providing the necessary augmentation to the distal portion of the femur.

Abstract: An impactor tool can include a handle, an impactor, a lock, an actuator, and a pin. The impactor can be coupled to the handle. The lock can be extendable from the impactor to engage an implant and retractable into the impactor to secure the lock and the impactor to the implant. The actuator can protrude from the impactor and can be coupled to the lock. The actuator can include a cam defined by a channel extending through the actuator. The pin can be coupled to the lock and disposed within the cam channel, where the actuator can be operable along a path defined by the cam and the pin to extend and retract the lock.

Abstract: The patient specific instrument (PSI) assembly for guiding a surgical tool on a tibia during a knee replacement surgery includes an extra-medullary portion at a distal end, an elongated rod connected at a distal end to the extra-medullary portion and extending in a direction along a mechanical axis of the tibia, and an upper mounting portion at a proximal end. The extra-medullary portion has a pair of spaced apart malleoli clamping elements with a size and/or relative position that is patient-specific for engaging respective ones of the lateral and medial malleoli. The upper mounting portion including a base body connected to a proximal end of the elongated rod and a surgical guide having guide openings extending therethrough and anchor element(s) on the upper mounting portion in locations adapted to overlay a peripheral contour of the tibia. The peripheral contour of the tibia including an anterior surface of the proximal tibia.

Abstract: A computer assisted surgery (CAS) system and method for preparing an anatomical structure to receive an orthopaedic implant. The method generally involves the steps of determining a contour of the anatomical structure by using the CAS system to acquire a plurality of points on the anatomical structure and provide a best fit approximation of the anatomical structure based on the plurality of points, selecting an implant to replicate the anatomical structure, and preparing the anatomical structure to receive the implant.

Abstract: A patient-specific pin guide for performing a total ankle arthroplasty can comprise a tibia pin guide, a talus pin guide and an interlocking component. A patient-specific cutting guide system for performing a total ankle arthroplasty can comprise a talus cutting guide and a tibia cutting guide. A method of performing a total ankle arthroplasty can comprise: coupling a patient-specific talus pin guide to a talus; coupling a patient-specific tibia pin guide to a tibia; positioning an interlocking device between the patient-specific tibia pin guide and the patient-specific talus pin guide; inserting guide pins into the patient-specific tibia and talus pin guides; removing the patient-specific talus and tibia pin guides from the guide pins; and coupling patient-specific talus and tibia cutting guides to the talus and tibia using at least some of the guide pins to alternatively perform resections on the tibia and talus.

Abstract: A patient-specific cutting assembly comprises a model file including geometrical data of a bone of the patient, of an intramedullary canal of the bone, and a planned orientation of a cutting block. A fixing rod is adapted to be longitudinally inserted in and extending partially from the intramedullary canal. A patient-specific cutting block is connectable to the fixing rod. The patient-specific cutting block includes a structure having a patient specific geometry corresponding to the model file of the patient, the structure configured to be connected to a portion of the fixing rod projecting from the bone in a unique coupling orientation. A cutting guide is connected to the structure, the cutting guide being in the planned orientation when the structure is connected to the portion of the fixing rod projecting from the bone.

Abstract: An instrument can comprise an instrument body, a cross-pin, and a ring. The instrument body can be configured to be partially inserted into an intramedullary canal of a bone having a bone resection. The cross-pin can extend through the instrument body, and the ring can be movably coupled to the cross-pin and positionable on the bone resection. The ring can be configured to pivot about a longitudinal axis of the cross-pin such that an angle of the ring relative to the instrument body approximates a surface angle of the bone resection relative to the instrument body. Additional apparatus, methods, and systems are disclosed.

Abstract: A system for creating a patient-specific jig model for patellar resurfacing surgery comprises a patellar implant positioning module for obtaining a planned position of a patellar implant on a model of the patella, the model being anatomically patient-specific. A patella resurfacing calculator module calculates a position and/or orientation of a resurfacing plane and attachment bore in the patella as a function of the planned position of the patellar implant.

Abstract: A surgeon can secure an acetabular component to an acetabular bone. The surgeon can insert a pair of anchors through a corresponding pair of holes in the acetabular component into a corresponding pair of pilot holes drilled into the acetabular bone. Each anchor is attached to a length of suture before insertion. The surgeon can tie the sutures from the anchors together, to secure the acetabular component against the acetabular bone. The surgeon can position the tied lengths of suture in a suture channel formed in the acetabular component. The suture channel can prevent the suture from interfering with a liner that contacts the acetabular component. The surgeon can repeat as needed, using multiple pairs of anchors, multiple holes and suture channels in the acetabular component, and multiple pilot holes in the acetabular bone. The surgeon can use soft anchors or screw anchors.

Abstract: A stem for fixating a prosthesis to a bone can include a first stem portion and a second stem portion. The first stern portion can extend substantially along a longitudinal axis. The first stem portion can include a distal portion. The second stem portion can extend substantially distally from the distal portion of the first stem portion along the longitudinal axis. The second stem portion can be securable to the bone, and the second stem portion can include a distal portion couplable to a compress assembly.

Abstract: An anatomy simulator can include a guide body having one or more faces. The anatomy simulator can include a first simulator socket forming a recess in a first face of the one or more faces. The first simulator socket can be configured to receive a first plate. The first simulator socket can include a first base portion. The anatomy simulator can include a bore extending from the base portion of the first simulator socket to an interior of the anatomy simulator. The bore can be configured to receive an alignment mechanism. The first base portion can be angled at a first angle with respect to the first face.

Abstract: The subject matter includes systems, methods, and prosthetic devices for joint reconstruction surgery. A computer-assisted intraoperating planning method can include accessing a first medical image providing a first view of a joint within a surgical site as well as receiving selection of a first component of a modular prosthetic device implanted in the first bone of the joint. The method continues by displaying a graphical representation of the first component of the modular prosthetic device overlaid on the first medical image, and updating a graphical representation of the first component based on receiving positioning inputs representative of an implant location of the first component relative to landmarks on the first bone visible within the first medical image. The method concludes by presenting a selection interface enabling visualization of additional components of the modular prosthetic device virtually connected to the first component and overlaid on the first medical image.

Abstract: Apparatuses and systems including at least one of mounting and removal of a femoral component on a femur are disclosed. The instrument can include a handle, a plunger, first and second arms and a knob. The handle can define a recess. The recess can extend along a portion of an elongate length of the handle. The plunger can be moveably disposed within the recess and can be configured to extend through an opening in a distal end of the handle to engage a pad to contact the pad against the femoral component. The first and second arms can be pivotally coupled to the handle and can be pivotable relative to one another. The first and second arms can each have at least one coupling feature configured to engage with a corresponding second coupling feature in the femoral component. The knob can be configured to operatively actuate the plunger to move the plunger proximal/distal within the recess to engage the plunger with and disengage the plunger from the pad.

Abstract: A joint alignment method comprises using imaging data of at least a portion of a leg to create a leg model, wherein the leg model includes a femur having medial and lateral condyles and a tibia having tibial plateaus that are configured to engage the medial and lateral condyles at a knee joint, displaying an image of the leg model for manipulation by a user, locating a pivot point within one of the medial or lateral condyles, and rotating, in the displayed image, the tibia with respect to the femur, about the pivot point, to obtain a desired knee joint articulation in a specified plane.

Abstract: Embodiments of a system and method for assessing hip arthroplasty component movement are generally described herein. A method may include receiving data from a sensor embedded in a femoral head component, the femoral head component configured to fit in an acetabular component, determining information about a magnetic field from the data, and outputting an indication of an orientation, coverage, or a force of the femoral head component relative to the acetabular component.

Abstract: According to one example, a posterior-stabilized femoral prosthesis for a knee arthroplasty. The femoral prosthesis can include medial and lateral condyles, a femoral cam and a recess. The medial and lateral condyles can be shaped to articulate with a tibial articular surface of a tibial bearing component through a range of motion, in which full extension corresponds to zero degrees flexion of a knee joint and positive flexion corresponds to greater than zero degrees flexion of the knee joint. In a sagittal plane, the medial and lateral condyles can define medial and lateral multi-radius curves, respectively. The medial multi-radius curve can have a single common radius swept through a first angular extent to define a single arc length that extends from between substantially ?20 degrees flexion to substantially 90 degrees flexion, inclusive.