An osteotomy assistance kit includes a bone treatment assistance device and an attaching position confirmation device. The attaching position confirmation device includes a feature point indication rod to be applied via a tip portion to a feature point of the bone, a rod support unit that removably supports the feature point indication rod such that the tip portion is indicating the feature point of the bone, and a second support member that movably supports the rod support unit and indicates one of scales on the rod support unit. The bone treatment assistance device includes cutting slits, and first guide holes that guides first rods set to a predetermined positional relation. The second support member of the attaching position confirmation device is attached to the protrusion of the bone treatment assistance device.

This disclosure relates to planning systems, methods and instrumentation. The planning systems, methods and instrumentation disclosed herein may be utilized for planning orthopaedic procedures to restore functionality to a joint, may include determining an amount of bone loss along or otherwise adjacent to an articular surface of a bone. Instrumentation may be formed based on one or more dimensions associated with the bone loss. The articular surface may be repaired, which may include utilizing the instrumentation and planning systems to position and secure a bone graft along a position of the bone associated with the bone loss.

There is a process for correcting a bone injury, an implant for correcting the bone injury and a kit for applying the implant for correcting the bone injury. The process can be made substantially uniform with the application of a standardized kit. In at least one application the process is for correcting a bunion on a patient. The process can include applying a first drill guide to a bone, and then a second drill guide. Once the drill guides have been applied and wires have been inserted into a bone, an implant can then be applied to correct a bone injury and to allow the bone injury to heal.

In accordance with one or more embodiments herein, a patellofemoral implant arrangement 200 for repairing damage in a patellofemoral articulation of a patient is provided. The patellofemoral implant arrangement 200 comprises a femoral trochlear implant 250, comprising an articulating surface 255, and a patellar implant 300, configured to be inserted, preferably with press-fit, into a recess 620 in a patella 600 in such a way that the perimeter of an articulating surface 310 of the patellar implant 300 does not extend beyond a surrounding articulating surface of the patella 600. The articulating surfaces 255, 310 of the femoral trochlear implant 250 and the patellar implant 300 are designed to allow that they at least partly interact with each other when the implants 250, 300 are implanted into the knee joint and the patella 600 lies in the intercondylar groove of the femur. Preferably, the articulating surface 255 of the femoral trochlear implant 250 is a metal or ceramic surface; and the articulating surface 310 of the patellar implant 300 is not a metal or ceramic surface. The articulating surface 310 of the patellar implant 300 may be designed to correspond to the curvature of a simulated healthy articulating surface of the undamaged patella 600 at the site of diseased cartilage. The contour curvature of the articulating surface 310 may be generated based on the determined surface curvature of the cartilage and/or the subchondral bone in a predetermined area comprising and surrounding the site of diseased cartilage and/or bone in the patella 600, to mimic the original, undamaged, articulating surface of the patella 600.

Certain systems, methods, and devices described herein are configured to dynamically model a patient area for surgery and/or other treatment, dynamically identify one or more features and/or characteristics thereon such as the length and/or elasticity of the posterior longitudinal ligament (PLL), dynamically allow modification of the model, dynamically limit and/or assist in modification of the model, and/or dynamically generate guidelines for generation of patient-specific implants and/or treatment kits for a specific patient.

A patient specific guide for hip replacement for patients undergoing hip replacement surgery. The guide works for correction of the acetabulum defects based on a finite element model, which detect the bone quality and guide the surgeons for the optimum screws trajectories. The guide surface reflects the acetabular morphology which provide a correct posting of the cup, especially for the complex case as bone loss, severe fractures and tumors. CT-scan images are used to construct the 3D model of the acetabulum bone, therefore a finite element and virtual surgery planning methods are applied to create the electronic file of the patient specific guide. In final step, the 3D printers are used to produce the patient specific guide.

An apparatus and a method are provided for a patient-specific instrument guide for arthroplasty or other operations on bone tissue, capable of limiting bone cuts, achieving optimal implant positioning, and providing improved stability of implants. The patient-specific instrument guide comprises a body that includes a bone contact surface configured to contact a bone surface of a patient. The body is configured to be 3D printed according to medical imaging of a patient's anatomy, such that the bone contact surface optimally contacts the surface of the patient's bone. The body includes one or more guide slots that each slidably receives a cutting guide. The cutting guides are configured to receive a saw blade during bone cutting. The cutting guides may be oriented to guide cutting a talus or a tibia during a total ankle arthroplasty surgery.

A method of designing a pair of fixation rods for implantation on a patient's spine includes: modelling the spine: determining a corrected vertebrae position; modelling the corrected spine by: realigning the vertebrae in the frontal plane, rotating the sacral plateau in the sagittal plane, modifying angulation in the sagittal plane between the adjacent plates of the discs, changing angulation between one or two vertebrae in the sagittal plane, and modifying the height of each disc; calculating a point cloud passing through the centers of the vertebral bodies; deducing two point clouds on either side of the first, spaced in the frontal plane by the width of the vertebra multiplied by X, and located in the sagittal plane at a distance equivalent to the depth of the vertebra in the sagittal plane multiplied by Y, X and Y being a function of the instrumentation connecting the rod to the spine.

A kit including (1) a plate configured to be secured to a scapular spine with a first end of the plate near a trigonum and a second end of the plate near an acromion; (2) a first hook including a mount, a first hook portion extending from the mount in a first direction, a spacer extending from the first hook portion in a transverse direction, and a second hook portion extending from an opposite end of the spacer in the first direction, the first hook adapted to extend around a lateral end of the acromion when fixed to the second end of the plate; and (3) a second hook including a mount, a curved portion curving away from the mount, and a hook portion at an opposite end of the curved portion, the second hook adapted to extend around the trigonum when fixed to the first end of the plate.

In one embodiment, an anatomical implant template has a template body having opposed first and second terminal ends. The template body bends so as to change the body from a first configuration, whereby the body extends from the first terminal end to the second terminal end along a first path, to a second configuration, whereby the body extends from the first terminal end to the second terminal end along a second path, different from the first path, the second path conforming more closely to the curvature of the at least one anatomical body. The body supports at least one device that outputs at least one signal from which a shape of the body in the second configuration can be ascertained. The anatomical implant template can further communicate the at least one signal to a computing device that generates signals for bending an anatomical implant.