Aspects of the present disclosure involve systems, methods, computer program products, manufacturing processes and the like, for utilizing a series of images of a patient's anatomy to determine an estimation of relevant lengths and angles and other dimensions for use during a hip replacement procedure, which may be used to create one or more femur and/or acetabulum cavity implants or inserts useful in a partial or total hip replacement. In one particular embodiment, a jig mechanism for providing a scraper of the acetabulum cavity may be created with the information of the patient's anatomy. Further, the location of these features in the images may be determined by analyzing the gray scale value of one or more pixels around a selected point on the image. The pixel with the lowest gray scale value may then be assumed to be the edge of the cortical bone in the 2D image.

A method of treating a sacroiliac joint including: approaching the sacroiliac joint with an implant including a sensor supported by a body; delivering the implant either a) non-transversely into the sacroiliac joint, b) transversely across the sacroiliac joint, or c) up to the sacroiliac joint without insertion therein, the sensor providing a signal that indicates a present condition of the sacroiliac joint; receiving an input from a sensory indicator based on the signal from the sensor, the sensory indicator being in communication with the sensor, and wherein the input from the sensory indicator provides data associated with the signal; and, treating an ailment of the sacroiliac joint based at least in part on the input.

A device for measuring femur bone displacement during total hip arthroplasty includes a base element immovably mounted to the pelvis and a measurement arm, detachably mounted to the base element via a support, and the measurement arm is fitted with a microprocessor computing system with a display screen. The measurement arm includes at least two movable links, serially connected with each other and with support by rotary joints with at least one (and preferably three) degrees of freedom, whereby both movable links are fitted with an accelerometer (preferably a three-axis accelerometer) and/or a magnetic field sensor and/or a gyroscope, preferably forming together an integrated acceleration, magnetic field and gyroscopic sensor unit.

Within examples, a surgical device with an embedded sensor system for performing hip replacements is described. This device mitigates fracturing of the mid metaphyseal/diaphyseal region of the femur, and ensures adequate press-fit of the component into the bone. The device relays information regarding forces experienced by the patient's bone to a separate data acquisition device and displays it on an interface. This information is used by the surgeon to determine the force present inside of the patient's bone during broaching, and can then be used to provide better care, and mitigate fractures due to overloading in the bone.

A device and associated method for measuring hamstring function, determining previous hamstring injury, predicting the risk for future injury, and controlling the return to sports play following such an injury.

Disclosed are methods and systems to provided planning tools for surgery, particularly for THA. Images of musculoskeletal structure of a patient (e.g. associated with respective planes and in a same or different functional position) may be displayed together and via co-registration and spatial transformations, 3D implants or other objects may be rendered and overlaid in a same position correctly with respect to each image. Measures may be represented with respect to various planes associated with the respective image and/or with respect to an existing implant. A safe zone (graphical element) may be rendered and overlaid with respect to each displayed image to indicate a clinically accepted safe range of positions for the 3D implant. Different instances of implants having respective characteristics affecting range of motion may be available for use during a procedure. For a set of available implants minimal and maximal safe zones may be presented for planning assistance.

A sacroiliac joint fusion procedure and implant designed for fixation in the dense bone of the SI joint inferior to the extra-articular recess. The implant includes an opening extending across the sacroiliac joint space, an iliac fixation member and a sacral fixation member connected to one another by a bridge where the pair of fixation members extend further distally than the bridge.

Methods for evaluating subjects having conditions associated with loss of muscle function (e.g., a motor neuron disease, a neuromuscular disease, or a myopathy) by measuring muscle function (e.g., muscle strength) are disclosed.

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, and joint alignment. The system further includes a remote system for receiving, processing, and displaying quantitative measurements from the sensors. 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. The kinetic assessment increases both performance and reliability of the installed joint by reducing error that is introduced by elements that load or modify the joint dynamics not taken into account by prior assessment methods.

Systems, methods and a sensor alignment mechanism are disclosed for medical navigational guidance systems. In one example, a system to make sterile a non-sterile optical sensor for use in navigational guidance during surgery includes a sterile drape having an optically transparent window to drape the optical sensor in a sterile barrier and a sensor alignment mechanism. The alignment mechanism secures the sensor through the drape in alignment with the window without breaching the sterile barrier and facilitates adjustment of the orientation of the optical sensor. The optical sensor may be aligned to view a surgical site when the alignment mechanism, assembled with the sterile drape and optical sensor, is attached to a bone. The alignment mechanism may be a lockable ball joint and facilitate orientation of the sensor in at least two degrees of freedom. A quick connect mechanism may couple the alignment mechanism to the bone.