Logic may determine how to reduce bone segments. Logic may communicate one or more images to display with at least two bone segments. Logic may identify a first reduction point and a third point on a first bone segment and identify a second reduction point and a fourth point on the second bone segment. Logic may identify a fifth point on the first bone segment and a sixth point on the second bone segment. Logic may also divide the one or more images along a line or plane between the bone segments, bring the second reduction point and the associated image segment to the first reduction point, align the line or plane of the second bone segment with a line or plane of the first bone segment. Furthermore, logic may adjust alignment and record the movement of the image segments or compare original and final positions, to determine deformity parameters.

Disclosed are a self-switching transmission assembly, a balloon, and a prosthesis for use in a shoulder joint. The self-switching transmission assembly comprises: a communicating tube (11, 11′, 11″) comprising an input end (111, 111′, 111″) and an output end (112, 112′, 112″); an external connection tube (12, 12′, 12″), an end portion thereof being insertable into the communicating tube (11, 11′, 11″) from the input end (111, 111′, 111″) and removable from the communicating tube (11, 11′, 11″) from the input end (111, 111′, 111″); and a sealing tube (13, 13′, 13″), which can be placed in a tube body of the communicating tube (11, 11′, 11″) and moved axially relative to the tube body of the communicating tube (11, 11′, 11″). The sealing tube (13, 13′, 13″) comprises a connection end (131, 131′, 131″) and a sealing end (132, 132′, 132″), the connection end (131, 131′, 131″) being detachably connected to the end portion of the external connection tube (12, 12′, 12″) by means of a connection driving mechanism, and the sealing end (132, 132′, 132″) being provided with a pass-through region, wherein, when the pass-through region is exposed outside of the output end (112, 112′, 112″), the self-switching transmission assembly is in a pass-through state, and when the pass-through region is placed inside the tube body of the communicating tube (11, 11′, 11″), the self-switching transmission assembly is in a sealed and blocked state.

A spinal correction rod implant manufacturing process includes: estimating a targeted spinal correction rod implant shape based on a patient specific spine shape correction and including spine 3D modeling, one or more simulation loops each including: first simulating an intermediate spinal correction rod implant shape from modeling mechanical interaction between the patient specific spine and: either, for the first simulation, the implant shape, or, for subsequent simulation, if any, an overbent implant shape resulting from the previous simulation loop, a second simulation of an implant shape overbending applied to the targeted spinal correction rod implant shape producing an overbent spinal correction rod implant shape representing a difference between: either, for the first loop, the targeted spinal correction rod implant shape, or, for subsequent loop, if any, the overbent spinal correction rod implant shape resulting from the previous simulation loop, and the intermediate spinal correction rod implant shape.

An orthopaedic surgical instrument includes a polymer cutting block having a number of metallic cutting guides secured thereto. A pair of metallic bushings function as saw stops at the medial and lateral ends of the cutting slot during an orthopaedic surgical procedure.

Antibacterial coatings and methods of making the antibacterial coatings are described herein. A first branched polyethylenimine (BPEI) layer is formed and a first glyoxal layer is formed on a surface of the BPEI layer. The first BPEI layer and the first glyoxal layer are cured to form a crosslinked BPEI coating. The first BPEI layer can be modified with superhydrophobic moieties, superhydrophilic moieties, or negatively charged moieties to increase the antifouling characteristics of the coating. The first BPEI layer can be modified with contact-killing bactericidal moieties to increase the bactericidal characteristics of the coating.

Provided is a kit for treating tissue of a subject. The kit includes a tool for creating a wedge opening within a bone tissue, and an implant. In some examples, the kit also includes an introducer configured to deliver the implant into the wedge opening.

A method of, and apparatus for, directing an elongate flexible component with a length through a part of a human body. The method includes the steps of: obtaining an apparatus having an elongate body with a length between axially spaced leading and trailing ends and a notch through a peripheral surface of the elongate body; directing a midlength part of the elongate flexible component into the notch to place the elongate flexible component into an operative position on the apparatus; and with the elongate flexible component in the operative position, advancing the elongate body through the part of the human body and thereby causing a portion of the elongate flexible component to be drawn by a drawing surface on the elongate body through the part of the human body.

A system for penetrating the lateral cortex of a long bone includes a tubular cortex penetrator having an inner surface and an outer surface, a proximal end, and a distal end comprising a beveled cutting edge configured to penetrate the lateral cortex. A guide wire is configured to pass over the tubular cortex penetrator, and a guide sleeve is configured to surround the outer surface of the tubular cortex penetrator. A hollow extraction screw with an axial bore, a proximal end, a distal end, and a threaded cutting edge is configured to pass through the axial bore of the hollow extraction screw; and the hollow extraction screw is configured to retract into a distal end of a bore through the tubular cortex penetrator.

The disclosure relates to a spacer using a hydrogel for treatment that aids in growth or bonding of living tissues after surgery or treatment of joints, muscles, or ligaments. The spacer includes a support sheet formed of a biodegradable hydrogel material having a water-soluble polymer network structure, and a pouch formed of a biodegradable material, as a sealing bag-shaped member surrounding the support sheet, and the support sheet is formed to dissolve in a body fluid faster than the pouch. Therefore, the spacer and a method of manufacturing the spacer according to the disclosure may eliminate cost and stress because there is no need for a subsequent removal operation, while stabilizing a surgical site and reducing pain, and particularly, adjust a drug delivery rate adaptively according to different recovery rates or tissue regeneration rates for different ages of patients.

The disclosure relates to a spacer using a hydrogel for treatment that aids in growth or bonding of living tissues after surgery or treatment of joints, muscles, or ligaments. The spacer includes a support sheet formed of a biodegradable hydrogel material having a water-soluble polymer network structure, and a pouch formed of a biodegradable material, as a sealing bag-shaped member surrounding the support sheet, and the support sheet is formed to dissolve in a body fluid faster than the pouch. Therefore, the spacer and a method of manufacturing the spacer according to the disclosure may eliminate cost and stress because there is no need for a subsequent removal operation, while stabilizing a surgical site and reducing pain, and particularly, adjust a drug delivery rate adaptively according to different recovery rates or tissue regeneration rates for different ages of patients.