Patent classifications
A61B17/8897
PATIENT-SPECIFIC PROSTHESIS ALIGNMENT
Systems and methods for providing alignment of instruments and/or prostheses in various surgical operations are provided herein. The systems and methods generally include one or more sensors coupled to a patient's bones or other surgical tools, the sensors can detect their position and orientation in space and communicate this information to a processor. The processor can utilize the information to display data to a surgeon or other user regarding the position, angle, and alignment of a patient's bones, surgical tools, and prostheses. Further, the one or more sensors can be aligned to the patient's anatomy using a patient-specific alignment guide that interfaces with a portion of the patient's anatomy in a single position/orientation.
BONE SLIVER REMOVAL SYSTEM
A surgical tool and related methods are provided for removal of a bone sliver from a resected joint. The tool can include a housing including an upper end, a lower end, and a channel extending from the upper end to the lower end. A paddle member extends from the lower end of the housing. The paddle member includes a paddle shaft and a paddle head. The surgical tool further includes an insertion member that has a handle end, an extension that extends from the handle end, and a cutting tip. The extension is translatable within the channel such that the handle end and the cutting tip can move relative to the housing between a retracted position and an advanced position.
Joint osteotomy system and method
A resection guide includes a first body portion and a second body portion. The first body portion has a first bone engagement structure and defines a first plurality of holes. The second body portion has a second bone engagement structure and defines a second plurality of holes. The first body portion and the second body portion are operable to separate a first anatomical structure of a patient and a second anatomical structure of the patient. A cutting guide defines at least one guide aperture that is operable for guiding a cutting tool for use in resecting a portion of the second anatomical structure of the patient. The cutting guide is positionable relative to the first body portion.
Systems and methods for percutaneous spinal interbody fusion (PSIF)
The present invention includes a novel procedure and corresponding medical devices for a Percutaneous Posterior Lumbar Interbody Fusion (PePLIF). In PePLIF, the surgeon performs the entire operation percutaneously without the use of a microscope, endoscope, or magnifying loupes. An adjustable retractor system is disclosed that enables the surgeon to percutaneously perform the surgery through accessing the facet joint (and later disc space) that was created by said retractor system. This retractor system provides the surgeon a safe area to work and operate without fear of damaging nerves, blood vessels, or other tissue. An expanding trial may be inserted into and removed from the disc space through the interior of the retractor system to determine the proper size for the expandable cage. The retractor system also enables the expandable cage to be inserted into the disc space.
PATIENT-SPECIFIC NAVIGATIONAL GUIDE
Patient-specific navigational guide (1) for use in spinal surgery, comprising two tubular guiding members (2) integral with a bearing frame (3) and extending from a proximal opening (2a) to a distal opening (2b) for guiding a surgical operation on a patient's vertebra (100); contact members (14, 15, 16) designed to match a corresponding plurality of contact areas (103, 102) on the patient's vertebra (100) in order to define a unique coupling configuration of the patient-specific navigational guide (1) on the patient's vertebra (100), wherein said contact members (14, 15, 16) comprise at east one pair of first main contact members (15), designed to abut on a contact area corresponding to the superior articular process (103) or facet of the patient's vertebra (100) and a pair of second main contact members (16), designed to abut at least partially on a contact area corresponding to the laminae (102) of the patient's vertebra (100). Contact members also comprise auxiliary contact members (14), designed to abut at least partially on a contact area corresponding to the edges (102a) of the patient's vertebra (100), in a position different from that of contact of the pair of the second main contact member (16), or to abut at least partially on a contact area corresponding to the transverse process (104).
DILATOR ASSEMBLY
A dilator assembly includes a blade, a tubular member defining a passage extending along a longitudinal axis, a guide needle received within the passage, a first link having a first end pivotally coupled to the tubular member and a second end pivotally coupled to the blade, and a second link having a first end pivotally coupled to the tubular member and a second end pivotally coupled to the blade.
Suprapatellar insertion system, kit and method
A system is provided for inserting and securing, through a suprapatellar region of a leg, a nail into a medullary canal of a bone. The system can include a flexible sleeve configured to be partially inserted in the leg. The flexible sleeve can define a leading end and a trailing end spaced apart from the leading end along a first axis. The flexible sleeve can define a first cannulation that extends along the first axis between the leading and trailing ends. The first cannulation can be sized to receive therethrough at least the intramedullary nail. The system can further include a retaining member configured support at least a portion of the flexible sleeve. The retaining member can be configured to position the flexible sleeve through the suprapatellar region of the leg such that the flexible sleeve leading end is aligned with the proximal end of the bone. The intramedullary nail can be insertable through the flexible sleeve and into the medullary canal.
Implant system for bone fixation
An implant system for use in orthopaedic surgery for fixation of bone includes an intramedullary nail and a coupling member. The intramedullary nail includes a proximal portion defining a longitudinal axis. The proximal portion includes an axial bore defining an axis substantially parallel to the longitudinal axis of the proximal portion and a transverse bore configured to receive a bone fastener. The coupling member includes a through hole and is movably arranged within the axial bore of the proximal portion. Further, the coupling member includes a drive portion and a bone fastener engagement portion. The drive portion is in one variant non-rotatably coupled to the bone fastener engagement portion. The bone fastener engagement portion is configured to engage the bone fastener penetrating the transverse bore. In one variant the engagement is realized via an extended contact region.
Surgical tools for spinal facet therapy to alleviate pain and related methods
Methods and surgical tools for treating back pain use a spinal facet debridement tool with cautery and denuding action and minimally invasive protocol that can denude and cauterize soft tissue associated with a synovial capsule of the spinal facet joint.
TOTAL WRIST PROSTHESIS AND RELATED METHODS
Disclosed is a wrist prosthesis, and methods for implanting same, the prosthesis comprising an elongated radial component having two opposite sides, the first side comprising a stem and the second side comprising a concave dish; an elongated carpal component having two opposite sides, the first side comprising a stem, and the second side comprising a ball end; a lunate component having two opposite sides, the first side comprising a cavity adapted to receive said carpal component's ball end, and the second side comprising a convex surface adapted to engage said radial component's concave dish; wherein said lunate component freely rotates and swivels with respect to both of said carpal and radial components; wherein said stem of said carpal component is adapted for rigid engagement with one or more carpal and/or metatarsal bones; and wherein said stem of said radial component is adapted for rigid engagement with a radius bone.