Abstract: A measurement system comprising a measurement device and a computer. The measurement device is configured to measure a force, pressure, or load applied by the musculoskeletal system. The measurement device comprises an enclosure and a structure configured to fit within an opening in the enclosure. The enclosure is hermetically sealed housing electronic circuitry and at least one sensor. The structure is configured to couple to the musculoskeletal system. At least three sensors underlie and couple to the structure to measure a force, pressure, or load applied to a surface of the structure. The structure includes at least three anti-cantilevering structures. At least one of the three anti-cantilevering structures is configured to couple to the enclosure to limit canting of the structure when the musculoskeletal system couples to the surface of the structure outside a predetermined area.

Abstract: A medical sensor is disclosed for mounting within a medical device. In one embodiment, more than one medical sensor is mounted to a printed circuit board using surface mount technology to accurately place the medical sensors in predetermined positions. The medical sensor is a sensor for measuring a force, pressure, or load. The medical sensor is manufactured in a process that supports consistency, matching, reliability, and performance. The medical sensor comprises a substrate, a dielectric layer overlying the substrate, and four strain gauges overlying the dielectric layer. Interconnect and pads are formed overlying the dielectric layer. The interconnect couples the four strain gauges into a full bridge Poisson gauge and couples the pads to the full bridge Poisson gauge. The active strain gauges are placed in a predetermined location on the substrate that support measurement of a force, pressure, or load applied to the substrate.

Abstract: Disclosed herein is a humeral head trial, a system for humeral trialing, and a method for removing a humeral head trial from a humeral stem. The humeral head trial may include a first portion, a second portion, and a post extending from the second portion. The first portion may define a convex articular surface with a movable surface substantially flush with the convex articular surface. The post may define a first length in a first configuration and a second length in a second configuration. The first length may be greater than the second length. The post may change from the first configuration to the second configuration by moving the movable surface with respect to the convex articular surface.

Abstract: An example method includes displaying, via a visualization device and overlaid on a portion of an anatomy of a patient viewable via the visualization device, a virtual model of the portion of the anatomy obtained from a virtual surgical plan for an orthopedic joint repair surgical procedure to attach a prosthetic to the anatomy; and displaying, via the visualization device and overlaid on the portion of the anatomy, a virtual guide that guides at least one of preparation of the anatomy for attachment of the prosthetic or attachment of the prosthetic to the anatomy.

Abstract: An example method includes displaying, via a visualization device and overlaid on a portion of an anatomy of a patient viewable via the visualization device, a virtual model of the portion of the anatomy obtained from a virtual surgical plan for an orthopedic joint repair surgical procedure to attach a prosthetic to the anatomy; and displaying, via the visualization device and overlaid on the portion of the anatomy, a virtual guide that guides at least one of preparation of the anatomy for attachment of the prosthetic or attachment of the prosthetic to the anatomy.

Abstract: A resection guide includes an anchor having bone anchoring features, a cutting block having a cutting guide defined therein, and a linkage flexibly connecting the cutting block to the anchor. The flexibility of the linkage provides the cutting block with six degrees of freedom of motion relative to the anchor.

Abstract: A joint replacement system that includes an acetabular cup implant that has an outer surface, a drill bit that has a cutting surface, and a guide separately formed from the acetabular cup implant. The guide has a body that defines first and second guide openings each adapted to receive the drill bit. The system also includes void filler prosthesis that has an implant facing surface and first and second portions connected to the implant facing surface. The first and second portions each have an outer surface that has a geometry corresponding to the cutting surface of the drill bit such that the first and second portions can be received in respective openings in a bone formed by the drill bit.

Abstract: A computing system generates, based on medical imaging data of bones of a joint of a patient, bony landmark data that characterizes relationships between two or more landmarks on one or more of the bones of the joint of the patient. Additionally, the computing system applies a classifier algorithm that has been trained using training data to select a class associated with the patient from among a plurality of classes. The classifier algorithm takes the bony landmark data of the patient as input.

Abstract: A bioactive filamentary structure includes a sheath coated with a mixture of synthetic bone graft particles and a polymer solution forming a scaffold structure. In forming such a structure, synthetic bone graft particles and a polymer solution are applied around a filamentary structure. A polymer is precipitated from the polymer solution such that the synthetic bone graft particles and the polymer coat the filamentary structure and the polymer is adhered to the synthetic bone graft particles to retain the graft particles.

Abstract: The tibial implant includes an integral baseplate, keel and four spikes. Each of the spikes include a non-tapering section and a tapering section, four free ends and four fillets. The spikes are specifically spaced about the baseplate and include porous outer surfaces adjacent to the baseplate.

Abstract: An example device includes a surgical item for use in a surgical procedure; and a light on or within the surgical item. In this example, the light is controllable by an external device so as to identify the surgical item for use in the surgical procedure.

Abstract: A system is disclosed herein for providing a kinetic assessment and preparation of a prosthetic joint comprising one or more prosthetic components. The system comprises a prosthetic component including sensors and circuitry configured to measure load, position of load on a curved surface, joint stability, range of motion, and impingement. In one embodiment, the system is for a ball and socket joint of a musculoskeletal system. The system further includes a computer having a display configured to graphical display quantitative measurement data to support rapid assimilation of the information. The kinetic assessment measures joint alignment under loading that will be similar to that of a final joint installation. The kinetic assessment can use trial or permanent prosthetic components. Furthermore, adjustments can be made to the applied load magnitude, position of load, and joint alignment by various means to fine-tune an installation.

Abstract: A device for use in orthopedic procedures involving the alignment and fixation of bone. The device includes a body having a bone facing surface, an opposing surface, a lateral surface being disposed between the bone facing surface and the opposing surface and a longitudinal axis extending through the bone facing surface and the opposing surface. The body defines a pin hole extending through the body from the bone facing surface to the opposing surface, a bone fastener hole extending through the body from the bone facing surface to the opposing surface, a tool hole extending at least partially through the body and an alignment index for positioning the body relative to bone.

Abstract: An implant is produced by fabricating first and second layers. The first layer of repeated and truncated building units is fused together to define pores. The second layer of repeated and truncated building units are fused together to define pores and fused onto the first layer of truncated building units. The first and the second layers form at least part of a porous portion of the implant. The formed porous portion is attached onto a base portion of an implant. The truncated building units of each of the first and the second layers are in the form of spatially overlapping three-dimensional shapes.

Abstract: A method of implanting a medical implant includes resecting a long bone along a shaft of the bone so as to form a resected surface and remove a metaphysis of the bone. A tapered bore is reamed through the resected surface of the long bone and into an intramedullary canal thereof. A tapered portion of a stem of a medical implant is fully seated within the tapered bore so as to form a press-fit between the tapered portion of the stem and the long bone and so that a collar disposed at an end of the stem is offset from the resected surface so as to form a gap between the resected surface and the collar.

Abstract: Various apparatus and methods for implanting glenoid prostheses are disclosed. In various embodiments, a kit for shoulder surgery can include a partial reaming guide having a patient-matched surface shaped to conform to a scapula of a patient, the partial reaming guide configured to limit glenoid reaming about a reaming axis to only a portion of a glenoid; and an anchor peg channel guide having a patient-matched surface shaped to conform to a portion of the glenoid, the anchor peg channel guide having a channel offset from the reaming axis.

Abstract: A method is disclosed for making a glenoid guide that includes obtaining scapula surface profile information of a specific patient, providing a manufacturing plan for making the glenoid guide having at least one patient specific contact surface configured to contact a portion of the glenoid rim or glenoid surface and for making the guide having a rotation control feature forming member, and adapting the manufacturing plan to specify the location of the rotation control forming feature relative to a portion of the glenoid determined to benefit from augmentation based on the surface profile information.

Abstract: Various embodiments disclosed herein relate to stemmed and stemless humeral anchors for use in shoulder arthroplasty procedures. For example, the humeral anchor can include a first end, a second end, and an interior surface extending between the first end and the second end. The interior surface can be disposed about a recess disposed between the first end and the second end. The recess can be configured to secure a coupling of a shoulder articular body directly to the interior surface.