Abstract: Various intramedullary implants, instruments, and methods are disclosed herein. In an example, a compression instrument is used to provide internal compression of bones adjoining a joint or bones spanning a fracture to cause compression of the joint or fracture.

Abstract: A modular transdermal assembly configured to couple an external prosthetic device to a bone stump. The assembly includes a modular transdermal portion and a bone fixator. The modular transdermal portion includes an interface portion configured to couple with the external prosthetic device. The bone fixator is configured to be secured to the bone stump and couple with the modular transdermal portion to retain the modular transdermal portion relative to the bone stump.

Abstract: A patient-specific guide tool for guiding an object toward a glenoid face of a scapula of a patient for implantation of a shoulder prosthetic device is disclosed. The guide tool includes a guide portion that includes a guide surface. The guide surface is configured to guide movement of the object toward the glenoid face. Furthermore, the guide tool includes a patient-specific portion that is operably coupled to the glenoid portion. The patient-specific portion includes at least one patient-specific surface that is three-dimensionally contoured and that is configured to nest and closely conform to a corresponding surface of the scapula to thereby position the guide surface at a predetermined position relative to the glenoid face.

Abstract: An impaction tip can be used in installing an implant. The impaction tip can comprise a body, and a sliding member. The body can have a handle-facing surface and an implant-facing surface. The body can define a grooved portion. The handle-facing surface can define an opening sized to receive a portion of an impaction handle. The sliding member can be located at least partially within the grooved portion. The sliding member can be slideable from an interior position to an exterior position. When the sliding member is in the exterior position a portion of the sliding member can contact the implant.

Abstract: A transdermal intraosseous device for coupling a bone stump to an external prosthetic device includes a bone fixator, an external connector and a plurality of modular interface components. The bone fixator includes a proximal portion configured for anchoring into the bone stump of the patient and a distal portion including a base collar configured for subcutaneous implantation. The external connector has a distal portion for coupling to the external prosthetic device and a proximal portion for coupling to the distal portion of the bone fixator. Each interface component can be removably coupled to the base collar and has different size and shape to provide a surgeon-selected transition between the prosthetic device and the patient's skin.

Abstract: A system for compressing a fracture can include a first bone plate having a first proximal end and a first distal end, and a second bone plate having a second proximal end and a second distal end. The second bone plate can be spaced apart from the first bone plate. The system can include an expansion member coupled to the second proximal end of the second bone plate. The movement of the expansion member relative to the second bone plate can cause the first distal end of the first bone plate and the second distal end of the second bone plate to move toward each other to compress the fracture.

Abstract: An offset guide can include a body, an arcuate portion, a first fin, and a second fin. The body can have a first surface. The arcuate portion can extend from the body and have a second surface. The first surface and the second surface can define an opening. The first fin can extend from the first surface into the opening. The second fin can extend from the first surface into the opening. A portion of the first surface can be located between the first fin and the second fin and arranged at an angle relative to a longitudinal axis of the offset guide.

Abstract: An alignment plate can be designed and formed based upon a known geometry of a subject, such as a human patient. The alignment plate can include various members, such as a plurality of fingers or legs, to contact the selected points of the anatomy. Based upon contact of the fingers at the selected points of the anatomy, the alignment plate can be aligned at a preselected or predetermined alignment with a portion of the anatomy, such as an acetabulum.

Abstract: A glenoid implant comprises a body comprising: an articular surface and a scapula-engaging surface, the scapula-engaging surface including first and second portions angled relative to each other; and a fixation feature extending from the scapula-engaging surface. A method comprises: forming a planar bone surface at a glenoid using a guide pin; forming a first bore into the glenoid located near the guide pin; forming a second bore into the glenoid offset from the first bore; inserting an augment ream guide into the first and second bores; and forming an angled bone surface at the glenoid relative to the planar bone surface using the augment ream guide. A ream guide comprises: a base having first and second surfaces; a bone peg extending from the first surface; an alignment peg spaced from the bone peg; and a guide peg extending from the second surface at an oblique angle to the bone peg.

Abstract: An acetabular prosthesis is described that includes a shell having an outer surface and an inner surface, the outer surface defining an external shape. There is at least one through bore extending from the outer surface of the shell to the inner surface of the shell. At least one augment is configured to be positioned at least partially within the at least one through bore of the shell such that, in an assembled state, the shell and the at least one augment define a modified external shape.

Abstract: A fluid powered gripper can include a body, a bore, a first finger, a second finger, and a piston. The body can include a central bore coaxial with a central longitudinal axis of the body. A bore fluid inlet can be fluidly coupleable to the central bore. The first finger can be rotatable about the body. The second finger can oppose the first finger and the second finger can be rotatable about the body. The piston can be disposed in the central bore. The piston can be powered by a fluid to move between a first position and a second position. The first finger and the second finger can be closed in the first position and open in the second position.

Abstract: A plate assembly for attaching a bone flap to a skull is provided and may include a first plate member attached to the bone flap and a second plate member supported by the first plate member and movable between a retracted position and an extended position relative to the first plate member. The second plate member may be removed from a cut line between the bone flap and the skull in the retracted position and may extend over the cut line in the extended position.

Abstract: A method of automatically registering a surgical navigation system to a patient's anatomy is provided. The method comprises programming a surgical navigation system with a first spatial relationship between a surgical component and a reference array connected to the surgical component, programming the surgical navigation system with a second spatial relationship between an anatomical feature of a patient and the surgical component, installing the surgical component on the patient such that the surgical component engages the anatomical feature in the second spatial relationship, and locating the reference array with the surgical navigation system. The navigation system automatically recognizes the position of the reference array relative to the patient's anatomy.

Abstract: A failsafe for a transdermal apparatus for a prosthetic appendage can include a first plate, a second plate, and a breakaway connector. The first plate can have a central axis, a proximal portion, and a distal end. The distal end can be opposite the proximal portion, and the distal end can be securable with a prosthetic external to skin and can be configured to simulate an appendage of a patient. The second plate can be aligned with the central axis and can include a proximal end and a distal portion. The proximal end can be securable to a transdermal implant, and can extend proximally from the second plate. The distal portion can be opposite the proximal end, and the distal portion can be configured to interface with the proximal portion of the first plate. The breakaway connector can be couplable within the second plate and the first plate.

Abstract: A method for preparing surgical kits for use during a surgery includes preparing a pre-operative surgical plan for a patient and selecting a set of surgical instruments based on the pre-operative surgical plan. The set of surgical instruments includes at least a general instrument, a first size-specific instrument, a patient-specific instrument, and a surgeon-specific instrument. The general instrument is selected from a predetermined group of off-the-shelf instruments. The first size-specific instrument has a first size selected from predetermined sizes. The patient-specific instrument includes a three-dimensional contoured engagement surface configured to nest into a portion of a native anatomy in a single location. The surgeon-specific instrument is selected based on a surgeon preference and is a different instrument than the selected general instrument, first size-specific instrument, and patient-specific instrument.

Abstract: A method for preparing a femur for receiving a prosthesis. The method includes the following: fixing a femoral trial component to the femur; coupling a reamer bushing relative to the femoral trial component; reaming a cavity into the femur using the reamer bushing as a guide; coupling at least one of a modular femoral box trial and a stem adapter relative to the femoral trial component; trialing the femoral trial component with the articulating surface of the femoral trial component; and performing the coupling of the reamer bushing, the reaming of the cavity, the coupling of the at least one of the modular femoral box trial and stem adapter, and the trialing of the femoral trial component all while the femoral trial component remains fixed to the distal femur.

Abstract: A cement mold assembly configured to form a temporary implant for use in delivering antibiotics to an infected site can includes a first mold and a second mold. The first mold can have an open end and an inner wall. The first mold can define a tibial component forming cavity including a platform forming cavity and a stem forming cavity. The second mold can have a body portion configured to be slidably and progressively receivable by the inner wall into the tibial component forming cavity in a direction toward the closed end. Progressive advancement of the second mold into the tibial component forming cavity urges cement within the tibial component forming cavity against the body portion and the inner wall to form a unitary tibial component having a tibial tray portion formed by the platform forming cavity and a stem portion formed by the stem forming cavity.

Abstract: An apparatus for preparing a bone for receiving a prosthesis comprises a template that can secure to the bone, a revision alignment member for coupling to the template, an offset alignment bushing receivable by the template such that an intramedullary member seated in the first bone can extend through a passage defined by the offset alignment bushing, a first bone cutting bushing receivable by the template after removal of the offset alignment bushing and positioned to cut the bone, a second bone cutting bushing receivable by the template after removal of the offset alignment bushing and removal of the bone cutting bushing, said second bone cutting bushing having a rotational orientation corresponding to a rotational orientation of the offset alignment bushing such that the second bone cutting bushing is a guide for cutting the bone in preparation of the bone to receive the prosthesis with an offset adapter.

Abstract: Various modular implants and modular implant systems are disclosed herein, as are methods of implanting the same. The modular implant systems can include modular implants that are stacked on each other to define a modular implant system, which in an example can be used to replace or augment a void in bone. The modular implants can interact with an intramedullary implant to, for instance, assist with a fusion procedure.

Abstract: A method of securing an orthopedic hip prosthesis to an acetabulum of a living being. The prosthesis can be a shell or a cup, and the surgery can be a total hip arthroplasty such as a revision total hip arthroplasty. In some examples the method can include placing an augment at a bone surface of the acetabulum, applying a layer of fixation material over the bone surface in an amount sufficient to cover the augment, and then implanting the prosthesis over the layer of fixation material to secure the prosthesis to the layer of fixation material. In various aspects of the method, the augment can be an anchor or a spacer.