Abstract: An intramedullary nail system including an elongated nail member comprising a cavity and electrically conductive at least in part, a coil assembly, a first electrode connected to a first pole of the coil assembly and a second electrode connected to a second pole of the coil assembly. To improve such an intramedullary nail system the coil assembly is provided in an end cap assembly that is proximally releasably connected to the nail member and with at least one electrically conductive outer contact surface. At least one section of the electrically conductive outer contact surface forms the first electrode and at least one section of the nail member forms the second electrode.

Abstract: A cable threader device for passing a guide cable between pedicle screws during minimally invasive spinal surgery, the device comprising a handle with a trigger mechanism, the handle mounted onto an elongated shaft having a curved free end with a detachable curved lead member retained in telescoping manner on the end of the body. The guide cable is affixed to the lead member, the instrument is inserted into a first screw tower, the trigger mechanism is activated to advance the lead member into the adjacent tower, and the lead member and guide cable are retrieved through the second tower.

Abstract: There is disclosed a device and method for stabilizing a bone. The device includes a polymer with a glass transition temperature. The polymer is relatively deformable at a temperature above the glass transition temperature and relatively rigid at a temperature below the glass transition temperature. The device, while the polymer is above the glass transition temperature, is responsive to a bending force to bend during insertion into the intramedullary canal of the bone. The device, while the polymer is below the glass transition temperature, is relatively rigid and able to provide reinforcement to the bone.

Abstract: The present invention provides a method for stabilizing a fractured bone. The method includes positioning an elongate rod in the medullary canal of the fractured bone and forming a passageway through the cortex of the bone. The passageway extends from the exterior surface of the bone to the medullary canal of the bone. The method also includes creating a bonding region on the elongate rod. The bonding region is generally aligned with the passageway of the cortex. Furthermore, the method includes positioning a fastener in the passageway of the cortex and on the bonding region of the elongate rod and thermally bonding the fastener to the bonding region of the elongate rod while the fastener is positioned in the passageway of the cortex.

Abstract: What is provided is a fixation system that offers a strong and stable construct for maximum fusion augmentation and yet is versatile enough for any patient and is easy to use. Disclosed is a connection assembly for connecting a spinal implant, the assembly comprising: a body, the body including a body opening for receiving at least a portion of a first connector; a swivel having first and second ends and being operatively connected to the body, the first end including a swivel opening for receiving at least a portion of a second connector; a locking plate having an arm at least partially extending into the body opening; a locking unit operatively connected to the body and contacting the second end of the swivel; and whereby activation of the locking unit causes the arm to engage the first connector and swivel opening to engage the second connector thereby preventing relative rotation between the first and second connectors.

Abstract: A unitary intervertebral device, having no moving components is provided for non-fusion articulation applications. The interbody articulating device allows for limited flexion and rotation between adjacent vertebrae, helping to preserve or restore near-normal motion between adjacent vertebrae. Rotational motion is achieved through one or more protrusions incorporated into the spinal interbody device. In one articulating form, a first protrusion extends perpendicularly from the superior aspect of the disc-shaped interbody device to form a spike or rotational protrusion, while a second protrusion extends axially from the inferior aspect of the interbody device to form a second spike or rotational protrusion. Protrusions preferably extend perpendicular from the apex of both the first and second arcuate articulating surfaces.

Abstract: A surgical portal apparatus includes a portal housing, a portal sleeve, and a seal. The portal housing defines a central housing axis and a central housing channel. The portal sleeve extends from the portal housing and is dimensioned to pass through tissue to provide access to underlying tissue via a longitudinal opening. The central housing channel of the portal housing and the longitudinal opening of the portal sleeve define a passageway for reception and passage of a surgical object. The seal has inner surfaces defining a seal passage for establishing a general sealed relation about the surgical object. The seal passage is radially offset with respect to the central housing axis. The seal is adapted to rotate about the central housing axis to vary positioning of the seal passage to substantially maintain the substantial sealed relation upon manipulation of the surgical object within the portal housing.

Abstract: This equipment comprises at least one connecting bar and at least one sacrum anchor assembly (1-3, 5). According to the invention, each sacrum anchor assembly comprises two sacral anchor screws (1, 2), a link assembly (3) including: a sacral connecting part (10) assembled to a sacral anchor plate (11) with polyaxiality, i.e. having possible multi-directional tilting relative to the said first screw (1), and possible pivot relative to the said sacral anchor plate (11); two nuts (5) able to be screwed onto the said shanks (9) of the said first and second screws (1, 2), a first nut (5) is able to clamp this part (10) against a bearing surface (8) formed in the said first screw (1), for tilt and pivot immobilisation of this part (10) relative to the said sacral anchor plate (11).

Abstract: The present teachings provide an implant. The implant can include an implant body partially defining at least one threaded aperture. The implant can also include a bone fastener including a threaded portion threadably engaged with the at least one threaded aperture. The threaded aperture can circumferentially surround no more than 180° of the bone fastener.

Abstract: The present disclosure relates to a surgical instrument having a first elongated member and a second elongated member and a connector pivotably interconnecting the first elongated member and the second elongated member, where the first elongated member includes a partially or completely circumscribed opening, and the second elongated member includes a partially or completely circumscribed opening, or a support configured to correspond to the partially or completely circumscribed opening of the first elongated member that when operated between an open or closed state, engages or disengages an object to fix, confine and/or extrude the object with or through the partially or completely circumscribed opening of the first elongated member.

Abstract: This system includes a retaining housing formed by a hole intended to receive the anchoring member and a retaining portion arranged on the anchoring member; said retaining housing is arranged in a part having a degree of elastic flexibility and is delimited by a continuous wall of this part; the retaining housing, on the side of a first axial end, forms a first collar forming a continuous circular projection capable of being elastically deformed by the retaining portion arranged on the anchoring member; the wall of said part delimiting the retaining housing also forms, on a second axial end, a second collar not able to be elastically deformed by said retaining portion.

Abstract: A spinal implant provides supplemental and dynamic fixation and/or stabilization of the spine via connection to one or more existing or new spinal fixation and/or stabilization spinal constructs. The supplementary spinal fixation/stabilization implant has a first attachment device configured to couple to an existing or new spinal fixation/stabilization construct and a second attachment device configured to couple to the existing or new spinal fixation/stabilization construct at a second location. The first and second attachment devices are joined to each other via a resilient connector that allows dynamic movement between the first and second attachment devices.

Abstract: An implantable orthopedic device. The device includes: a proximal anchor, configured to be implanted inside a first metatarsal; the anchor having a collar larger than the opening in a metatarsal in which the proximal anchor is implanted; the collar preventing cable to bone contact; a distal anchor, configured to be implanted inside a second metatarsal, adjacent to the first metatarsal; the distal anchor having a male thread, a nut threadable onto the male thread of the distal anchor, and a cord mechanically interconnecting the proximal and distal anchors. A shock absorber includes an elongate housing threadedly positioned within the anchor; the shock absorber accommodates a cord holder mechanically connected to the housing via a damping member, the cord holder is freely rotatable within the housing to prevent the cord from twist kinking when the housing is rotated to adjust a tension force.

Abstract: A device has a capacitive surface and a light source. A user of the device uses the capacitive surface to change the intensity of light emitted by the light source. To increase and decrease the intensity of the light emitted by the light source, the user touches the capacitive surface with one or more fingers.

Abstract: An ophthalmic illuminator is provided that includes a pulse generator to provide amplified pulses and an amplifier to amplify the current pulses to produce amplified pulses. A light source within the ophthalmic illuminator is driven by the amplified pulses so as to stroboscopically illuminate a vibrating ophthalmic surgical tool within the interior of an eye.

Abstract: A bone anchor coupler assembly is configured to couple a bone anchor to a spine stabilization member, and includes a coupler body and an angular adjustment member movably coupled to the coupler body.

Abstract: A vaginal dilator for use in gynecologic examination. The vaginal dilator comprises an upper dilating member and a lower dilating member that are hinged to each other, the upper dilating member comprising an upper dilating leaf and an upper press rod arranged at a tail portion of the upper dilating leaf, the lower dilating member comprising a lower dilating leaf and a lower press rod arranged at a tail portion of the lower dilating leaf. The upper dilating leaf is hinged to the upper press rod, and the upper rod is hinged to the lower dilating member, and the upper press rod is provided with a light emitting element, a switch and a power source, the switch being connected with the light emitting element. The upper dilating leaf is pressed down to contact and mate with the upper press rod or the upper dilating leaf is disengaged from the upper press rod to coordinately control the switch to be connected to or disconnected from the power source.

Abstract: A tissue retractor generally includes a pair of arms that are pivotally coupled to each other and each have a finger grip portion on a first end and a working portion arranged on an opposite second end. Each of the second ends comprises an elongated shaft that extends along an axis. A pair of paddles each having a planar engagement body and a mounting portion are pivotally coupled to a corresponding elongated shaft. The paddles are selectively rotatable around the respective axes.

Abstract: A fixation clamp for use in an external fixation clamp has a clamping assembly having a reception to accommodate a fixation element. The clamp has a locking element extending through the clamping assembly for blocking the position in a defined angular position. A washer is arranged between the locking element and a central opening of the clamping assembly having a cutout extending radially from the through opening such that the washer is mountable and demountable in a radial direction to a locking element longitudinal axis. The cutout has a smaller distance between its sidewalls then the diameter of the through opening. The locking element has circular cross-section below its head portion adapted to fit through the through opening of the washer but larger than the opening of the cutout and has at least one pair of parallel beveled surfaces spaced closer than the distance between sidewalls of the washer cutout.

Abstract: Tissue spacer implants, surgical distraction instruments, surgical insertion tools, coupling devices, surgical kits, surgical methods for distraction, and methods for coupling bodies are disclosed. The tissue spacer implants include a first end member, a second end member, and an intermediate spacer member having a coupling mechanism adapted to couple the first end member with the intermediate spacer member and to couple the second end member with the intermediate spacer member. The surgical instruments may be used for inserting these implants and include a first elongated member, a second elongated member, a distraction mechanism, and an actuator. The coupling devices may be used to couple the components of the implants.