A system includes a cartridge having an elongate body extending from a first end to a second end and having a top side and a bottom side. The cartridge defines a first hole adjacent to the first end that extends through the cartridge from the bottom side to the top side. The top side of the cartridge defines a pair of parallel slots that extend perpendicular with respect to a longitudinal axis of the cartridge. Each slot of the pair of parallel slots is equidistant from a central axis defined by the first hole.

A distal femoral joint replacement system includes a femoral component having condylar articular surfaces, a stem extending from the femoral component, and a void filler for filling a bone void within a femur. The void filler includes a body and a plurality of legs extending from the body. The body has a sidewall defining an opening for receipt of the stem which extends along a length of the body and extends through the sidewall so as to form a side-slot in the sidewall that extends along an entire length of the sidewall. The plurality of legs each have a first end connected to the body and a second end remote from the body. The legs each have an outer surface that tapers between the first and second ends and is configured to register with a corresponding inner surface of a bone void when implanted in an end of the femur.

A device for implanting an intramedullary nail includes a base member and an adjustable member coupled together and translatable relative to each other along a direction. The device includes an insertion handle configured to carry the nail and mount to the adjustable member. A drill guide is attachable to the base member and configured to carry one or more guide sleeves for alignment with locking holes of the intramedullary nail. A first reference member extends from the base or adjustable member and has a first contact portion configured to contact an exterior location of a patient's limb. A second reference member extends from the other of the base and adjustable members and has a second contact portion configured to contact another exterior location of the limb. At least one of the first and second reference members is positionally adjustable relative to the base or adjustable member from which it extends.

A broach handle for a rasp includes a proximal part extending along a first axis between a first portion of the handle and a second portion of the handle, and a proximal part extending partially along a second axis between a third portion of the handle, connected to the second portion, and a fourth portion of the handle, and partially along a third axis between a fifth portion of the handle, connected to the fourth portion, and a sixth portion of the handle connectable to a rasp. The sixth portion of the handle has a connection surface for connecting to the rasp having a normal extending along a normal axis defining a connection axis between the handle and the rasp. A first convex angle is defined between the first axis and the second axis, and a second convex angle is defined between the third axis and the normal axis.

A guidance tool includes a body having a length extending from a first end to a second end. The body includes a shape memory section along the length of the body. The shape memory section has a curved shape.

Devices for treating a bone and methods of inserting such devices into a bone are disclosed. A device for treating a bone may include a flexible tube, a stiffening mechanism and an actuator. The flexible tube has a distal end and a proximal end. The stiffening mechanism within the flexible tube is configured to cause the flexible tube to become rigid. The actuator is configured to cause the stiffening mechanism to cause the flexible tube to become rigid in response to the actuator being actuated.

A medical device for penetrating a bone structure including a processing unit having a transfer function that associates an electrical conductivity value S with a depth value d, wherein the processing unit is configured to detect a threshold selected from amongst an absolute threshold, a relative threshold and a critical gradient, and to emit a warning signal and/or control signal responsive to detection of the threshold.

Various exemplary surgical impacting tool interfaces and methods of using surgical impacting tool interfaces are provided. In general, a surgical impacting tool includes a locking assembly configured to releasably attach to an adapter. In response to engagement with the adapter, the locking assembly is configured to move from an unlocked configuration, in which the adapter is not releasably attached to the surgical impacting tool (nor is any other adapter releasably attached to the surgical impacting tool via the locking assembly), to a locked configuration, in which the adapter is releasably attached to the surgical impacting tool via the locking assembly. The locking assembly is configured to receive the adapter in a longitudinal direction along a longitudinal axis defined by the locking assembly and to automatically lock the adapter to the surgical impacting tool.

An orthopedic instrument for insertion of an orthopedic device into an intramedullary canal of a bone is disclosed. The orthopedic instrument can include an elongate post and a stud. The post can have a longitudinal axis and can extend along the longitudinal axis between a first end portion and a second end portion. The stud can be connected to the post along a portion of a longitudinal length thereof comprising a first end part, A second part of the stud can be free to elastically deflect laterally with respect to the longitudinal axis when subjected to a bending load and return to a first position when unloaded.

A tibial baseplate system is described. While the system can include any suitable component, in some instances, it includes tibial baseplate having a first and second surface, the second surface being substantially opposite to the first surface, which is configured to be seated on a resected surface at a proximal end of a tibia. In some cases, the baseplate also includes a first spacer coupling that is configured to couple a first spacer to at least one of a lateral side and a medial side of the baseplate such that the spacer is disposed between, and is configured to maintain a set minimal distance between, the proximal end of the tibia and a distal end of a femur when the tibial baseplate is seated on the resected surface at the proximal end of the tibia and the spacer is coupled to the tibial baseplate. Other implementations are discussed.