Abstract: A system, apparatus and methods for providing a single use imaging device having improved viewing for sterile environments is disclosed and described. A single use high definition camera used for general purpose surgical procedures including, but not limited to, arthroscopic, laparoscopic, gynecologic, and urologic procedures, may comprise an imaging device that is a sterile and designed to ensure single use. The imaging device may further include a sensor located near the tip of a laparoscope and a view optimizing assembly.

Abstract: An osteotomy guide (100,500,600) guides cutting of a bone (300). The guide (100,500,600) has an anterior end (106,506,606) and a posterior end (108,508,608) that are spaced from one another along a transverse direction. The guide (100,500,600) has an inner surface (102,502,602) that faces the bone (300), and an outer surface (104,504,604) opposite the inner surface (102,502,602) along an outer direction (Do). The guide (100,500,600) includes a transverse guide surface (138,538,638) that extends along a transverse axis (AT) along the transverse direction so as to define a transverse cutting path into the bone (300). The guide (100,500,600) includes an ascending guide surface (134,534,634) that extends along an ascending axis (AA) along an ascending direction so as to define an ascending cutting path into the bone (300). The transverse and ascending axes (AT,AA) intersect one another.

Abstract: Arcuate fixation members with varying configurations and/or features are provided, along with additional components for use therewith in provided fixation systems and intervertebral implant systems. The arcuate fixation members may be of varying lengths, cross sectional geometries, and/or cross sectional areas, and may be configured with various features such as heads configured to accept other fixation system components, tabs to allow arcuate fixation member-in-arcuate fixation member or fixation anchor-in-arcuate fixation member configurations. Applications of fixation systems and intervertebral implants systems utilizing arcuate fixation members are particularly suitable when a linear line-of-approach for delivering fixation members is undesirable.

Abstract: A cerclage system used to affix a bone includes a tension plate, a cable lock, and a cerclage cable configured to encircle the bone. The tension plate, which is engageable with the cerclage cable, is moveable between a natural shape and an insertion shape where the tension plate stores energy. The cable lock locks the cerclage cable about the bone in engagement with the tension plate. The tension plate is configured for positioning atop the bone while residing in the insertion shape. The tension plate, through an engagement thereof with the cerclage cable and upon attempted movement thereof from the insertion shape toward the natural shape, delivers the energy stored therein to the cerclage cable thereby tensioning the cerclage cable such that the cerclage system continuously compresses the bone.

Abstract: A stem portion is formed such that when implanted in a scapula the stem portion includes three cross-sections parallel to a medial lateral plane. The middle cross-section has a length in the medial-lateral direction which is shorter than the lengths of the other two cross-sections in the medial lateral direction.

Abstract: Patient-mounted retractors with varying configurations and/or features are provided, along with additional components for use therewith in provided patient-mounted retractor assemblies. Blade type and tube type patient-mounted retractors that may be re-positioned during the course of a procedure are provided in varying configurations and/or geometries suitable for vayring procedures and/or patient anatomies. Applications of re-positionable patient-mounted retractor assemblies are particularly suitable for use in minimally invasive procedures, eliminating the need for table-mounted retraction assemblies and/or cannulas that restrict the operating envrionment.

Abstract: A bone transport device may include a first support member, a second support member, a plurality of first rods, a cable, and a plurality of actuator assemblies. The cable may be configured to be received through a first bone segment. The bone transport device may further include a second rod that is configured to extend through the first bone segment such that the cable abuts a portion of the second rod within the first bone segment. The plurality of actuator assemblies may be attached to the first support member or the second support member. Each of the plurality of actuator assemblies may include a body, a spool, and an actuator. The actuator may be configured to rotate the spool to wind the cable onto the spool and translate a second bone segment with respect to the first support member and the second support member.

Abstract: An orthopaedic surgical instrument includes an assembly collar having a cavity extending between a superior opening and an inferior opening. The cavity is sized to receive a tapered trunnion of an implanted femoral stem. A bore extends between an inferior end and a superior end of the assembly collar and is configured to align with an implant bore formed in the implanted femoral stem. The bore and the implant bore are configured to receive a fastener to secure the assembly collar to the implanted femoral stem. A method of utilizing the orthopaedic surgical instrument is also contemplated.

Abstract: An osteotomy guide (100) includes an inner surface (102) that faces the bone (300), and an outer surface (104) opposite the inner surface (102) along an outward direction (Do). The inner surface (102) defines proximal and distal bone contacting regions (118,120) that are spaced from one another by a gap (124) that extends into the inner surface (102) towards the outer surface (104). The guide (100) includes an ascending guide surface (134) that extends along an ascending direction so as to define an ascending cutting path into the bone (300). The guide (100) includes a transverse guide surface (138) that extends along a transverse direction so as to define a transverse cutting path into the bone (300).

Abstract: An intervertebral fusion device comprising inferior and superior fusion cage devices that provide an ability to correct spondylolisthesis via in-situ adjustment.

Abstract: A system for monitoring the ossification of an internally fixated fracture in a bone of a subject includes an implantable fixation device and an external wireless reader operative to transmit relative load data experienced by a bone plate across a fracture to a data server where trends in the change in added bone-support provided by the bone plate may be visualized. The implantable fixation device includes a primary load sensor and a reference load sensor, where a load value from the reference load sensor may be used to normalize the load value from the primary load sensor. The external wireless reader is in wireless communication with the implantable fixation device and is operative to receive a signal indicative of the load from each load sensor and to energize each load sensor via inductive charging.

Abstract: An assembly at a proximal end of an intravascular delivery system can allow the proximal end of a pull wire to move independently of a delivery tube. The assembly can generally include the pull wire, the delivery tube, a feature to prevent the proximal end of the pull wire from becoming inaccessible due to distal movement of the pull wire, and a feature to protect the proximal end of the pull wire from inadvertent, premature manipulation. When the intravascular delivery system is navigating tortuous vasculature, the proximal end of the pull wire can move distally in relation to the proximal end of delivery tube, relieving stress on the distal end of the pull wire. The proximal end of the pull wire can be protected from inadvertent manipulation during delivery and made available for manipulation once the distal end of the delivery system is in place.

Abstract: A system and method that acquire (i) at least a reference image including one of a preoperative image of a surgical site with skeletal and articulating bones and a contralateral image on an opposite side of the patient from the surgical site and (ii) at least an intraoperative image of the site after an implant has been affixed to the articulating bone. The system generates at least one reference landmark point on at least one anatomical feature on the articulating bone in the reference image and at least one intraoperative landmark point on that anatomical feature in the intraoperative image. The reference and intraoperative images are compared and differences between the orientation of the articulating bone in the two images are utilized to analyze at least one of offset and length differential.

Abstract: An electrical circuitry fitted to be connected or to be an integral part of a bone fixation device having at least one linear actuator coupled between two rings, including: at least one linear actuator connector, mechanically and/or electrically connectable to said at least one linear actuator; a control circuitry, wherein said control circuitry measures a value related to the movement of said at least one linear actuator and/or to the distance or change in distance between said two rings, by receiving signals from said linear actuator connector; and a memory, wherein said memory stores said value.

Abstract: A set for treating the vasculature to reduce or block blood flow includes a tray having at least three sections and a center recess configured to receive a mixing container. A sealed vial containing an ethiodized oil is disposed in a first section of the tray. A mixing container is disposed in a first section of the tray. A sealed tube containing a predetermined amount of n-Butyl Cyanoacrylate (“n-BCA”) is disposed in a second section of the tray. The sealed tube has an external thread. A self-piercing luer cap is disposed in the third section of the tray. The cap has an internal thread that mates with the external thread of the sealed tube of n-BCA. A luer lock syringe is disposed in one of the at least three sections of the tray.

Abstract: A dilation introducer for orthopedic surgery is provided for minimally invasive access for insertion of an intervertebral implant. The dilation introducer may be used to provide an access position through Kambin's triangle from a posterolateral approach. A first dilator tube with a first longitudinal axis is provided. An access cannula may be introduced over the first dilator tube. A drill may be inserted through the access cannula and used to perform a foraminoplasty. Surgical instruments may pass through the access cannula to operate on an intervertebral disc and/or insert an intervertebral implant.

Abstract: Techniques for addressing various technical problems associated with managing medical devices and data related to medical devices, for instance medical implants in a graphics case or medical device kit, are described herein. One or more medical device handling applications can execute on a medical device computer system. Such a computer system can include one more computing devices, such as for example a client device and a server device, that can optionally communicate with each other to send and receive information associated with medical devices. The computer system can further include a wearable device and a server device that can optionally communicate with each other to send and receive information associated with medical devices and medical device kits.

Abstract: A talar implant system and method in one embodiment includes an articulation component with an articulating surface extending upwardly from a first plane and configured to articulate with a tibial component, and a distal portion for implanting in a bone, the distal portion having a longitudinal axis and configured to be rigidly coupled with respect to the first plane at any angular position selected from a range of angular positions within a second plane perpendicular to the first plane.

Abstract: A method of stabilizing a first vertebra and a second vertebra includes implanting a first bone anchor into the first vertebra, implanting a second bone anchor into the second vertebra, connecting a first anchor connection instrument to the first anchor, connecting a second anchor connection instrument the second anchor, positioning a cement delivery tube into a passage provided through the first anchor, delivering bone cement from a bone cement delivery system coupled to the bone cement delivery tube through the passage in the first anchor to the first vertebra, removing the cement delivery tube from the first anchor connection instrument and the first anchor, connecting the cement delivery tube to second anchor connecting instrument connected to the second anchor, delivering bone cement through a passage in the second anchor to the second vertebra, connecting a spinal connection element to the first anchor and the second anchor.