Abstract: A femoral prosthesis system for an orthopaedic hip implant and method of use is disclosed. The prosthesis system includes a femoral stem component that includes a core body and a casing that encases the core body. The casing can be additively manufactured such that the core body defines a predetermined orientation in the core body among a plurality of permissible predetermined orientations. The femoral stem component can further include a neck and a trunnion that extends from the neck. The neck can extend out with respect to the core body at a predetermined angle within a range of permissible predetermined angles.

Abstract: A number of orthopaedic surgical instruments for use in a surgical procedure to prepare a patient's femur to receive an orthopedic prosthesis. The tools include guide tools, cutting tools, surgical blocks, and other orthopaedic surgical instruments configured to plan and guide the preparation of the patient's femur. A method of using the orthopaedic surgical instruments is also disclosed.

Abstract: A femoral prosthesis system for an orthopaedic hip implant and method of use is disclosed. The prosthesis system includes a femoral stem component that includes a core body and a casing that encases the core body. The casing can be additively manufactured such that the core body defines a predetermined orientation in the core body among a plurality of permissible predetermined orientations. The femoral stem component can further include a neck and a trunnion that extends from the neck. The neck can extend out with respect to the core body at a predetermined angle within a range of permissible predetermined angles.

Abstract: Disclosed is a central augment. The central augment can include a body and a protrusion. The body can include a first curved surface shaped to interface with a central portion of a bone and a second surface opposite the first curved surface and defining a recess sized to receive a portion of a prosthetic component. The protrusion can extend from the second surface within the recess.

Abstract: Disclosed is a central augment. The central augment can include a body and a protrusion. The body can include a first curved surface shaped to interface with a central portion of a bone and a second surface opposite the first curved surface and defining a recess sized to receive a portion of a prosthetic component. The protrusion can extend from the second surface within the recess.

Abstract: There is provided a tibial component comprising: a tibial tray with an inferior side; and a support member connected to the inferior side of the tibial tray, the support member having a stem portion, the support member further comprising at least one opening. In one embodiment, the at least one opening is constructed and arranged to receive a sawblade or an osteotome. In another embodiment, the at least one opening is comprised of solid material but is radio-lucent. In yet another embodiment, the at least one opening is comprised of solid material and is frangible.

Abstract: A prosthetic implant system for reconstructing a knee joint comprises a prosthetic implant and sleeve. The prosthetic implant comprises a tibial tray component for reconstructing a tibia of the knee joint, and a stem configured to extend from the tibial tray component to anchor the tibial tray component in the tibia of the knee joint. The sleeve comprises an outer wall configured to engage with bone, and an inner bore configured to receive the stem. The inner bore is shaped to couple to the prosthetic implant at a first location proximate the tibial tray component while surrounding the stem, and uncouple from the prosthetic implant at a second location spaced from the first location while still surrounding the stem. Methods employing the prosthetic implant system can comprise intraoperatively determining to use the sleeve in a coupled or un-coupled configuration based on a depth of a broach into a broached channel.

Abstract: Augments for implantation of an orthopedic implant device in a bone. A distal end of an outer portion of the augment can have a shape that is configured to generally conform to the shape of a metaphyseal-diaphyseal junction of an intramedullary canal of the bone. Further, a proximal end of the outer portion of the augment has a shape that is configured to generally conform to a shape of the metaphyseal region of the intramedullary canal. Additionally, the shape of the outer portion at the distal end can be separated from the shape of the outer portion at the proximal end by a distance that is approximately equal to the distance between the metaphyseal-diaphyseal junction and the metaphyseal region of the intramedullary canal.

Abstract: According to one example, a tibial replacement assembly for a knee arthroplasty can be configured to couple to a resected proximal surface of a tibia of a human knee. The tibial replacement assembly can include a tibial tray and a first spike. The tibial tray can include a proximal surface and a distal surface opposing the proximal surface. The distal surface can be configured to be disposed on a resected proximal surface of a tibia. The first spike can be removably secured to the tibial tray and can extend generally distally away from the distal surface. The first spike can be configured to extend beneath the resected proximal surface of the tibia.

Abstract: A stemless prosthetic shoulder joint may include a prosthetic humeral head and a stemless base. The stemless base may include a collar and an anchor extending from the collar intended to anchor the base into the proximal humerus. The anchor may include various features to enhance the fixation of the base, including hooks, threads, and/or expandable members that may be transitioned from a contracted insertion condition to an expanded implanted condition once the base is positioned in the bone. The anchor and/or collar may also include additional features to enhance fixation, such as geometries and surface features to enhance fixation to bone. The anchor may include a plurality of chisel slots to facilitate removal of bone during a revision surgery.

Abstract: An image processing apparatus according to the present disclosure includes a data acquisition unit configured to acquire data in which three-dimensional medical image data and supplementary information are associated with each other, a cross section information acquisition unit configured to acquire the supplementary information from the data and acquire cross section information indicating a cross section based on the supplementary information, a cross-sectional image generation unit configured to generate cross-sectional image data corresponding to the cross section based on the three-dimensional medical image data and the cross section information, and a display control unit configured to cause a display unit to display an image based on the cross-sectional image data.

Abstract: An implant system comprises an implant plate adapted to be positioned on a surface of a resected bone. The implant plate has a plurality of openings. A plurality of independently positionable pegs attach the implant plate to the bone. Each peg has a longitudinal axis and comprises: a peg body and a retaining device. The peg body is inserted into a peg hole in the bone. The peg body has a transverse dimension in a direction normal to the longitudinal axis, the transverse dimension larger than the openings of the plate. The retaining device is separate from the peg body, and is configured to attach to the peg body, with at least a first portion of the retaining device positioned above an upper surface of the implant plate, and a connecting portion of the retaining device extending through one of the openings of the implant plate.

Abstract: A method of attaching prosthetic implants to bone, applicable to tibia, patella, acetabulum, glenoid, or femur, includes trimming an articular surface of the bone, leaving a trimmed surface. Holes are punched or drilled into the surface in a predetermined array before polymethyl methacrylate bone cement is used to attach the surface to the implant. In an embodiment, the holes are punched by placing a punch-plate with sharpened punch spikes on the surface, and striking the punch plate to drive punches into the trimmed surface. In another embodiment, holes are drilled using a drilling template with predrilled guidance holes placed on the surface of the bone. In another embodiment, holes are drilled by positioning a robotic drill over the trimmed surface; adjusting a drilling pattern of the robotic drill according to the trimmed surface; and using the robotic drill to drill holes of predetermined depth according to the drilling pattern.

Abstract: Disclosed herein are systems, methods, and devices for providing a tibial implant including an anatomic stem that provides a close interface between the implant and surrounding bone. The stem varies in size, cross-sectional shape, or orientation from a proximal portion of the stem to the tip of the stem. The variation of the stem accommodates the variation of tibial anatomy into which the implant component is implanted. The stem provides resistance against rotation of the implant and reduces stress shielding effects by transmitting forces into surrounding bone. In certain implementations, the interface between the stem and bone is supplemented by fin extensions that extend outward from the stem and increase the contact between the implant and the surrounding bone structure.

Abstract: An orthopedic knee prosthesis is provided including a tibial baseplate component having a distal, bone-contacting surface with one or more fixation structures extending distally therefrom, in which the fixation structures are asymmetrically arranged within the baseplate periphery.

Abstract: A method of implanting a prosthetic knee joint assembly. The method includes: coupling a femoral component to a femur, and coupling a tibial component to a tibia; coupling a ligament link to one of the femur or the tibia; coupling the ligament link to a coupling component of one of the femoral component or the tibial component; arranging the ligament link in a first position relative to the tibial component when the prosthetic knee joint assembly is implanted in a left knee; and arranging the ligament link in a second position relative to the tibial component when the prosthetic knee joint assembly is implanted in a right knee, the second position is different from the first position.

Abstract: Methods, systems and apparatuses are disclosed including apparatuses that can be used in a total knee replacement procedure. According to one example, a tibial implant is disclosed. The tibial implant can be configured for attachment to a tibia in a knee arthroplasty and can include a baseplate having a lateral portion and a medial portion oriented relative to an anteroposterior axis and a fixation member. Each of the lateral portion and the medial portion can have a distal surface configured to interface with a resected proximal surface of a tibia. The fixation member can be coupled to and extend both distally and medially from the baseplate such that the fixation member is oriented at an acute angle relative to the distal surface of the medial portion.

Abstract: An orthopedic prosthesis assembly includes a first prosthetic component, a second prosthetic component, a retainer, and a fastener and allows the removal of the first prosthetic component without having to remove the second prosthetic component from an intramedullary canal of a patient's bone. The fastener is received in an aperture of the first prosthetic component and the retainer is configured to engage the aperture of the first prosthetic component such that a part of the fastener is secured within the aperture. A rod of the fastener is configured to advance along the longitudinal axis through the first prosthetic component into the second prosthetic component. The end of the rod of the fastener is threaded into a threaded bore defined in the second prosthetic component.

Abstract: A method of implanting a prosthesis based on bone density of a bone is provided. A first bone density of the bone may be determined at a first portion of the bone. A second bone density of the bone may be determined at a second portion of the bone. A first desired amount of bone removal may be determined at the first portion of the bone based on the first bone density. A second desired amount of bone removal may be determined at the second portion of the bone based on the second bone density. The desired amounts of bone may be removed from the first and second portions of the bone. A prosthesis may be selected and implanted.

Abstract: A kit for use in performing joint arthroplasty on a head of a long bone is disclosed. The kit includes: a first implant including a first implant articulating surface and an opposed first implant mounting surface having a first implant location feature; and an instrument for preparing a cavity in the head of the long bone. The instrument includes a body and a punch extending from the body. The punch includes a portion thereof having a shape similar to the first implant location surface of the implant. A method for providing joint arthroplasty is also disclosed.

Abstract: A fixed-bearing prosthesis includes a femoral component having a medial condyle surface and a lateral condyle surface. The knee prosthesis also includes a bearing having a medial bearing surface configured to articulate with the medial condyle surface of the femoral component, and a lateral bearing surface configured to articulate with the lateral condyle surface of the femoral component. A tibial tray is secured to the bearing. The tibial tray has a platform with an elongated stem extending downwardly from a lower surface thereof. A posterior buttress extends along a posterior section of the perimeter of the tray's platform, and an anterior buttress extends along an anterior section of the perimeter of the tray's platform. Differently-sized tibial trays are interchangeable with differently-sized bearings.

Abstract: A system is provided which includes an articulating component, a post, a reception member and a bone engaging member. The articulating component includes an articulating surface and a second surface opposite the articulating surface. The post is disposed below the second surface. The reception member is configured to receive the post. The bone engaging member is configured to be embedded in a bone, wherein the bone engaging member is configured to receive the reception member. The reception member includes a reception member inside surface, wherein the reception member inside surface faces the post when the post is received by the reception member. A first portion of the reception member inside surface defines a tapered configuration and the reception member inside surface comprises at least one ratchet interface.

Abstract: An orthopaedic surgical instrument includes a cup including an outer surface having an opening positioned on a component-engaging side and an inner wall extending from the opening of the outer surface to a back wall. The inner wall having a plurality of stepped surfaces facing the component-engaging side. Each of the plurality of stepped surfaces is sized to receive a platform of a tibial tray.

Abstract: An infection treatment system includes a first intramedullary rod for placement within an intramedullary canal and including a superior portion having a superior end, an inferior portion having an inferior end, and a shaft extending longitudinally between the superior and inferior portions. The shaft includes longitudinally extending channels. A second intramedullary rod for placement within an intramedullary canal includes a superior portion having a superior end, an inferior portion having an inferior end, and a shaft extending longitudinally between the superior and inferior portions. The shaft includes longitudinally extending channels. A coupler is operatively attached to the rods. The coupler has a superior face, an inferior face, an anterior face, a posterior face, a first lateral face and a second lateral face. At least one of the faces includes at least one opening in fluid communication with at least a portion of the channels of the first and second rods.

Abstract: An orthopedic 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 prosthetic tibial component for a knee joint, said prosthetic tibial component comprising: a base construct for engaging the tibia; and a bearing construct for engaging the femoral side of the knee joint; said bearing construct being adjustably fixedly mountable to said base construct.

Abstract: An orthopaedic tibial prosthesis includes a tibial baseplate with features designed for use with small-stature knee-replacement patients. The tibial prosthesis may include a shortened tibial keel, tibial keel fins which define a large angle with respect to a longitudinal axis of the keel, and/or tibial keel fins which extend along less than the entire longitudinal extent of the keel.

Abstract: An orthopaedic surgical instrument and method includes securing an anchor to a tibial prosthetic component implanted in a proximal end of a patient's tibia, moving a separator posteriorly toward the anchor to position a tip of the separator between a lower side of the tibial tray and an upper end of the tibial sleeve, advancing the separator from anterior to posterior between the lower side of the tibial tray and the upper end of the tibial sleeve to detach the tibial tray from the tibial sleeve, and removing the tibial tray from the proximal end of the patient's tibia. The tibial prosthetic component includes a tibial tray and a tibial sleeve secured to the tibial tray.

Abstract: An orthopaedic tibial prosthesis includes a tibial baseplate with an asymmetric periphery which promotes proper positioning and orientation on a resected tibia, while also facilitating enhanced kinematics, soft-tissue interaction, and long-term fixation of the complete knee prosthesis. The asymmetric baseplate periphery is sized and shaped to substantially match portions of the periphery of a typical resected proximal tibial surface, such that proper location and orientation is evident by resting the baseplate on the tibia. The baseplate periphery provides strategically positioned relief and/or clearance between the baseplate periphery and bone periphery, such as in the posterior-medial portion to prevent deep-flexion component impingement, and in the anterior-lateral portion to avoid undue interaction between the anatomic iliotibial band and prosthesis components.

Abstract: A stack-up assembly for tibial insert trial is provided. The stack-up assembly for tibial insert trial is inserted between a femoral component and a tibial component of an artificial knee joint. The stack-up assembly for tibial insert trial includes an insert trial body and a plurality of first augments. The insert body is operatively connected with the femoral component. The first augments are stacked between the tibial component and the insert trial body.

Abstract: A family of tibial baseplates can comprise a plurality of tibial baseplates. Each of the plurality of tibial baseplates can define a common nominal baseplate size and a unique, non-congruent tibial baseplate periphery as compared to the other tibial baseplates of the family of tibial baseplates.

Abstract: A modular knee prosthesis system includes a femoral component having a stem and a sleeve. The system is modular, and provides the surgeon with the option of distally offsetting the joint line by controlling the relative axial positions of the stem and the sleeve. Alternative options include providing sleeves with tapered bores of different diameters, providing a shim to be placed between the sleeve and the stem and providing the stems as adapters having different diameters.

Abstract: Disclosed herein are systems, methods, and devices for providing a tibial implant including an anatomic stem that provides a close interface between the implant and surrounding bone. The stem varies in size, cross-sectional shape, or orientation from a proximal portion of the stem to the tip of the stem. The variation of the stem accommodates the variation of tibial anatomy into which the implant component is implanted. The stem provides resistance against rotation of the implant and reduces stress shielding effects by transmitting forces into surrounding bone. In certain implementations, the interface between the stem and bone is supplemented by fin extensions that extend outward from the stem and increase the contact between the implant and the surrounding bone structure.

Abstract: Disclosed herein are systems and methods for filling bone voids which may be present at the time of surgery. The systems disclosed herein generally include a baseplate component, a spacer component, and void filler component. The spacer component is generally assembled to the baseplate component with a taper or press-fit, for example, in one of a plurality of selected axial positions. The void filler component is then generally assembled to the spacer component in one of a plurality of selected axial positions. The void filler component preferably has an outer surface with portions having varying diameters such that the outer surface thereof can be received within a canal of a bone and contact the bone forming the canal at different locations in order to aid in stabilizing the assembled components in the canal.

Abstract: A method of assembling a knee joint prosthesis for replacing a portion of a knee joint. The method includes rotatably coupling a post to an extension portion of an insert extending from a bearing member, and coupling a femoral component for articulation on the bearing member.

Abstract: The invention concerns a tibial prosthetic component comprising a plate (100) for forming a tibial plateau of a tibia (16), wherein a peripheral region of the plate (100) has a thickness of less than 3 mm. The invention also concerns a tibial prosthetic component having a keel of depth less than 9 mm. The invention also concerns a method of selecting a tibial prosthetic component comprising receiving measurements of at least one physical attribute of an individual into whom the tibial prosthetic component is to be implanted, selecting a thickness of a plate (100) and depth of keel of the tibial prosthetic component based on the measurements and providing a tibial prosthetic component comprising a plate (100) having the selected thickness and a keel having the selected depth.

Abstract: A tibial support structure includes a platform portion and a medullary portion that are monolithically formed as a single piece. The medullary and platform portions of the augment component are adapted to accommodate and mechanically attach to a tibial baseplate, and are individually shaped and sized to replace damaged bone stock both within the tibia, as well at the tibial proximal surface. The monolithic formation of the tibial support structure provides a strong and stable foundation for a tibial baseplate and facilitates restoration of the anatomic joint line, even where substantial resections of the proximal tibia have been made. The tibial support structure may be made of a bone-ingrowth material which facilitates preservation and rebuilding of the proximal tibia after implantation, while also preserving the restored joint line by allowing revision surgeries to be performed without removal of the tibial support structure.

Abstract: Certain embodiments generally provide an improved tibial base member comprising keel portions that allow one or both cruciate ligaments to be preserved. Other embodiments provide improved lateral and/or medial inserts having a mesial lip that helps relieve and/or prevent impingement between the femoral component and the tibial eminence. Other embodiments provide improved femoral components having various chamfers to provide additional clearance with respect to the tibial eminence and posterior cruciate ligament without decreasing bone coverage.

Abstract: An improved implant having components comprising an oxidized zirconium bearing surface adapted to decrease pain, lower friction, and minimize wear when coupled with natural femoral articular cartilage. The improved implant components also provide for reduced backside wear effects in fixed and mobile implants. The improved implant components further provide for more ideal wear coupling between components in mobile bearing implants.

Abstract: An orthopedic prosthesis includes a tibial implant and a tibial insert. The tibial implant includes an upper surface, a medial side, a lateral side and a first locking structure provided on the upper surface where the medial side and the lateral side of the tibial implant are defined by a medial-lateral midline. The tibial insert includes a second locking structure provided on its bottom surface. The first and second locking structures are configured for engaging each other along an engagement direction vector when the tibial insert is inserted into the tibial base towards the posterior side. The engagement direction vector is angled away from the medial-lateral midline of the tibial implant towards the medial side of the tibial implant by a predetermine angle.

Abstract: An orthopaedic prosthesis for cementless fixation has a solid metal base and porous metal pegs extending out from the base. The pegs are mechanically, rather than metallurgically, fixed to the base. A process for making such a prosthesis is also disclosed.

Abstract: A knee joint prosthesis is disclosed. The knee joint prosthesis can include a tibial baseplate, a tibial insert, and a spine. The tibial baseplate can include a tibial plateau, having a proximal surface and an opposing distal surface, and a tibial stem extending from the distal surface of the tibial plateau. The tibial insert can be located on the proximal surface of the tibial plateau and can include an aperture. The spine can extend through the aperture of the tibial insert and into a cavity of the tibial stem, from the proximal surface of the tibial plateau. The spine can be rotatable with respect to the tibial baseplate and the tibial insert. The knee joint prosthesis can further include a femoral component including a posteriorly-located femoral cam. The posteriorly-located femoral cam can engage the spine during movement of the knee joint prosthesis.

Abstract: An implant providing for both short and long term stability and fixation is disclosed. The implant includes a plurality of projections extending from a bone contacting surface, and a porous material covering at least portions of the surface and projections. The orientation of the projections and the porous material provide for the stability and fixation. Methods of forming and utilizing the implant are also disclosed.

Abstract: A knee prosthesis for use during performance of a knee replacement procedure includes a plurality of stem components in a range of various sizes, a plurality of femoral components in a range of various sizes, and a plurality of tibial trays in a range of various sizes. Each of the stem components is compatible with each of the femoral components and the tibal trays. Some of the stem components have a single slot formed therein, with other stem components having a pair of slots formed therein.

Abstract: A method for removing a stem portion of an orthopedic implant from a bone comprises exposing an implanted orthopedic implant having a body portion, a stem portion interconnected to the body and a porous metal section forming an interconnection between the body and the stem portion. A cutting tool is mounted on a holder connected to an exposed surface of the orthopedic implant. The porous section is aligned with the cutting tool mounted on the holder. The entire porous section is cut by moving the cutting tool therethrough in a direction transverse to the stem portion axis. The implant body portion is then removed and then the stem portion is removed from the bone. The cutting tool may be a saw or chisel which may be mounted on a guide fixed to the body portion.

Abstract: An orthopaedic knee prosthesis is provided including a tibial baseplate component having a distal, bone-contacting surface with one or more fixation structures extending distally therefrom, in which the fixation structures are asymmetrically arranged within the baseplate periphery.

Abstract: A tibial insert includes a base and a post extending from the base along a longitudinal axis. The post has a medial surface, a lateral surface, and a height along the longitudinal axis. The medial surface has a medial section, and the lateral surface has a lateral section oriented substantially parallel to the medial section. The medial section and the lateral section each have a width in a substantially anterior-posterior direction that is sufficient to enable varus/valgus constraint over a flexion/extension range from extension to about 90 to 120 degrees of flexion when the tibial insert is mated with a femoral component.

Abstract: Various embodiments of methods for obtaining kinematic information regarding a joint, including information regarding the joint in a weight-bearing position, are disclosed, as well as methods of designing implants, instruments, and surgical repair systems based on the kinematic information.

Abstract: A cementless orthopedic implant is disclosed. More specifically, but not necessarily entirely, a cementless tibial implant used as a component of a knee joint is disclosed. The tibial component may comprise a tibial tray and stem. The tibial component may be a monoblock design used for both primary and revision surgeries. The stem of the tibial component may comprise a plurality of protruding steps that assist in providing primary fixation and stability without the use of screws or cement. The stem of the tibial component may further comprise a first and second stepped wing portions.

Abstract: An orthopaedic implant for filling voids in bones, and methods of using the same. The orthopaedic implant comprises an open porous metal component, having pores for promoting bone regeneration, and a resorbable bone growth promoting component which is resorbed into new bone. The orthopaedic implant and methods of the present disclosure provide structural support for the bone as well as osteoconductive and/or osteoinductive matrix for promoting bone re-growth within bone void. Advantageously, the orthopaedic implants and methods disclosed herein are useful in filling critically sized bone voids.