Disclosed herein are rasp adapters, rasp systems, and method of use thereof. The rasp adapter can include a body and a retention element. The body can define a body cavity, a handle opening, and a trunnion bore. The retention element can be located within the body cavity and can include a knuckle and a heal. The knuckle can be located proximate to and movable into and out of the trunnion bore. The heal can be located proximate the handle opening. Movement of the retention element due to a force applied to the heal can cause movement of the retention element and movement of the knuckle into the trunnion bore.

A proposed treatment of arthrosis/osteoarthritis in a joint of a mammal or human patient involves deposing a liquid material on at least one damaged surface of the joint. To accomplish this, a reservoir (110) is provided, which holds a volume of a biocompatible material in liquid form outside of a body containing the joint (J) to be treated. A proximal end (P) of a tub e-shaped instrument (120) is connected to the reservoir (110), and a distal end (D) of the instrument (120) is inserted into the joint (J). The liquid material is fed through the instrument (120) to the distal end (D) for deposition on the at least one damaged joint surface.

The material is configured to assume a solid form under predefined conditions (e.g. when cooling off, or being exposed to a specific type of radiation). When the material has the solid form, it has a resistance to wear adapted to replace a worn out joint surface.

A medical device for treating hip joint osteoarthritis by providing a joint surface is provided. The medical device comprises at least two artificial hip joint surface parts, wherein said at least two artificial hip joint surface parts are adapted to be connected to each other to form an artificial hip joint surface during an operation. Furthermore a method of treating a hip joint of a human patient by providing said the medical device is provided. The hip joint comprising a caput femur and an acetabulum, the method comprises the steps of: cutting the skin of said human patient, dissecting an area of the pelvic bone on the opposite side from said acetabulum, creating a hole in said dissected area, said hole passing through said pelvic bone and into said hip joint of said human patient, and providing said medical device to said hip joint, through said hole in said pelvic bone of said human patient.

An orthopedic trial apparatus (100) including an orthopedic component (110) having a distal shaft portion (112) positionable within a passage in a bone and a proximal shaft portion (114) extending from the distal shaft portion, and a proximal trial assembly (120) engaged with the proximal shaft portion of the orthopedic component. The proximal trial assembly includes a proximal spacer (130) component and a proximal trial component (150). The proximal spacer component is rotationally engaged with the proximal shaft portion of the orthopedic component to substantially prevent relative rotation therebetween about a longitudinal axis. The proximal trial component is axially coupled to the proximal spacer component to prevent disengagement of the proximal trial component from the proximal spacer component while permitting selective rotation of the proximal trial component relative to the proximal spacer component about the longitudinal axis.

The invention provides a targeting device suitable for use in removing a femoral implant from the surrounding tissue, wherein the device comprises: (A) an anterior guide member (1), (B) a posterior guide member (4), (C) an engagement member (7), (D) a first pair of parallel connector rails (509, 510), and (E) an adjustment system (13). When the anterior guide member and the posterior guide member are connected by the first pair of connector rails, via the engagement member, the angled channels of the anterior guide member and the posterior guide member converge in the direction of a distal end, with the convergence angle of the angled channels being in the range of from 2 to 6 degrees, such as from 2 to 5 degrees.

An orthopaedic reamer includes a shell and a cutting tooth arrangement formed in the shell. The cutting tooth arrangement includes a cutting tooth having a predefined profile with a cutting edge having a cutting depth, and a depth-of-cut feature positioned forward of the cutting tooth, relative to a direction of movement of the shell at the location of the cutting tooth. The depth-of-cut feature has a control depth which controls a cutting depth of the cutting tooth during surgery.

An electrically driven orthopedic impactor may include an adapter for interfacing between the adapter and a surgical implement. The adapter may have a first surface that transmits a forward impact energy and a second surface that transmits a reverse impact energy. The adapter can connect to the surgical implement and to the orthopedic impactor without the use of external tools. The adapter may connect to the impactor via a pushing motion and may disconnect from the impactor via a reciprocal sleeve. A sensor can communicate a spatial orientation of the adapter with respect to at least one reference point that is not located on the adapter or the impactor. A communication device may transmit frequency information or impact energy information to the impactor based on a type of surgical implement attached to the adapter.

The present application is directed a Joint Revision Surgery Apparatus which includes a blade guide block which has a plurality of blade guide slots and a central cavity. The blade guide block central cavity is positioned over the trunnion end of the existing prosthesis to be removed and secured to the prothesis. Straight, curved and compound curved knife blades are guided by the blade guide slots to cut the prothesis free. The securing of the guide blade block support apparatus against the femur is accomplished by the means of a male threaded T handle screw or male threaded eyebolt threading into one of the female threaded orifices in the blade guide block frame. The guide blocks in varying sizes and configurations, straight and curved knifes blades and related accessories may be sold as a complete kit. The Joint Revision Surgery Apparatus facilitates rapid, efficient and complete removal of an existing prosthesis during joint revision surgery.

The present inventions relate to devices and methods that improve the positioning and fit of orthopedic reconstructive joint replacement stem implants relative to existing methods. For example, an embodiment of the device provides a stem component comprising proximal and distal body portions that can be configured to mimic a geometric shape of a central cavity region created in a bone of a joint for improving conformance and fixation of the stem component thereto. Further, another embodiment provides a system of stem implants that each have a unique medial offset for facilitating the matching of an implant to the geometry of a central cavity region of a bone. Additionally, an inclination angle of a resection surface of each of the implants in the system can remain constant or vary as a function of the medial offset.

A minimally invasive surgical procedure for replacing a hip joint is provided. A main incision is initiated at a point being a projection of a tip of a greater trochanter and extends proximally about a distance in the range of from 1 cm to 8 cm in line with the femoral axis. An inline capsulotomy is performed, while keeping muscles and posterior capsule intact, to expose the hip joint capsule for accessing the hip joint. The femoral canal is prepared for receipt of a femoral implant. The femoral head is resected and removed out of the acetabulum. A step of acetabular preparation is performed using a retractor comprising two tip rails, each tip rail having a plurality of tines. Related tools, devices, systems and methods are also provided.