Abstract: A novel conduit design is disclosed. The conduit includes a cylindrical body having defined therein a first aperture and a second aperture, wherein the first aperture is designed to receive a shaft of a turbine and the second aperture is sufficiently large to facilitate ingress or egress of a probe through the second aperture, and wherein the second aperture is located a distance away from the first aperture such that when a turbine is disposed through the first aperture, an entry by a probe into the cylindrical body through the second aperture is not prevented by presence of the turbine.

Abstract: A method and system for the creation or modification of the wear surface of orthopedic joints, involving the preparation and use of one or more partially or fully preformed and procured components, adapted for insertion and placement into the body and at the joint site. In a preferred embodiment, component(s) can be partially cured and generally formed ex vivo and further and further formed in vivo at the joint site to enhance conformance and improve long term performance. In another embodiment, a preformed balloon or composite material can be inserted into the joint site and filled with a flowable biomaterial in situ to conform to the joint site. In yet another embodiment, the preformed component(s) can be fully cured and formed ex vivo and optionally further fitted and secured at the joint site.

Abstract: A system and method for rejuvenating skin through ablation using a handheld device (200) having a removable treatment component (213) with an abrasive material on one surface of the component which surface is on a portion of the treatment component (213) configured to conform to a skin surface. The system further includes application of other elements to facilitate skin recovery and rejuvenation processes.

Abstract: A monolithic interpositional arthroplasty implant for use in repairing gyngylmus joints such as the joints of the ankle. The implant is a monolithic tibiotalar implant having a first major surface shaped to be positioned against a tibia. The tibia is allowed to articulate across the first major surface. A second major surface is shaped to be positioned against the talus.

Abstract: A system and method for rejuvenating skin through ablation using a handheld device (200) having a removable treatment component (213) with an abrasive material on one surface of the component which surface is on a portion of the treatment component (213) configured to conform to a skin surface. The system further includes application of other elements to facilitate skin recovery and rejuvenation processes.

Abstract: A generally spherical turbine configured to rotate transversely within a cylindrical pipe under the power of fluid flowing either direction therethrough is operatively coupled with a rotating machine or generator to produce electricity. In one embodiment, the blades of the spherical turbine curve in an approximately 180 degree arc in a plane that is at an inclined angle relative to the rotational axis of a central shaft. In another embodiment, a deflector is provided upstream of the spherical turbine and within the cylindrical pipe to control flow through the spherical turbine by shielding a part thereof. The blades of the spherical turbine are airfoil in cross section to optimize hydrodynamic flow, to minimize cavitation, and to maximize conversion from axial to rotating energy.

Abstract: A turbine is described. The turbine includes: (i) a shaft capable of rotation along its longitudinal axis and capable of connecting to an electrical generator, and the shaft having disposed thereon at least one shaft hinge; (ii) a radial arm including a first end having disposed thereon at least one first hinge; and a hinge pin that fits inside a cavity formed when at least one the shaft hinge of the shaft is in an engaged position with at least one first hinge of the radial arm, and in the engaged position the hinge pin capable of connecting the radial arm to the shaft.

Abstract: A generally spherical turbine configured to rotate transversely within a cylindrical pipe under the power of fluid flowing either direction therethrough is operatively coupled with a rotating machine or generator to produce electricity. In one embodiment, the blades of the spherical turbine curve in an approximately 180 degree arc in a plane that is at an inclined angle relative to the rotational axis of a central shaft. In another embodiment, a deflector is provided upstream of the spherical turbine and within the cylindrical pipe to control flow through the spherical turbine by shielding a part thereof. The blades of the spherical turbine are airfoil in cross section to optimize hydrodynamic flow, to minimize cavitation, and to maximize conversion from axial to rotating energy.

Abstract: A method and system for the creation or modification of the wear surface of orthopedic joints, involving the preparation and use of one or more partially or fully preformed and procured components, adapted for insertion and placement into the body and at the joint site. In a preferred embodiment, component(s) can be partially cured and generally formed ex vivo and further and further formed in vivo at the joint site to enhance conformance and improve long term performance. In another embodiment, a preformed balloon or composite material can be inserted into the joint site and filled with a flowable biomaterial in situ to conform to the joint site. In yet another embodiment, the preformed component(s) can be fully cured and formed ex vivo and optionally further fitted and secured at the joint site.

Abstract: A helical turbine configured to rotate transversely within a cylindrical pipe under the power of fluid flowing either direction therethrough is operatively coupled with a rotating machine or generator to produce work or electricity. The twisted blades of the turbine define a right circular cylinder when the shaft mounting them rotates under the influence of fluid flow through the pipe. In one embodiment, baffles are provided at least upstream of the cylindrical turbine and within the cylindrical pipe to control flow through the cylindrical turbine. The twisted blades of the helical turbine are airfoil in cross section, as are the radial struts or spokes that mount the twisted blades to the rotatable shaft, thereby to optimize hydrodynamic flow, to minimize cavitation, and to maximize conversion from axial to rotating energy.

Abstract: A generally spherical turbine configured to rotate transversely within a cylindrical pipe under the power of fluid flowing either direction therethrough is operatively coupled with a rotating machine or generator to produce electricity. In one embodiment, the blades of the spherical turbine curve in an approximately 180 degree arc in a plane that is at an inclined angle relative to the rotational axis of a central shaft. In another embodiment, a deflector is provided upstream of the spherical turbine and within the cylindrical pipe to control flow through the spherical turbine by shielding a part thereof. The blades of the spherical turbine are airfoil in cross section to optimize hydrodynamic flow, to minimize cavitation, and to maximize conversion from axial to rotating energy.

Abstract: A method and system for the creation or modification of the wear surface of orthopedic joints, involving the preparation and use of one or more partially or fully preformed and procured components, adapted for insertion and placement into the body and at the joint site. In a preferred embodiment, component(s) can be partially cured and generally formed ex vivo and further and further formed in vivo at the joint site to enhance conformance and improve long term performance. In another embodiment, a preformed balloon or composite material can be inserted into the joint site and filled with a flowable biomaterial in situ to conform to the joint site. In yet another embodiment, the preformed component(s) can be fully cured and formed ex vivo and optionally further fitted and secured at the joint site.

Abstract: An apparatus for delivery of an elongate member into the lumen of a trans-dermal catheter. In a preferred embodiment, the apparatus comprises a protective sheath configured to at least substantially surround an elongate member; and slidable member configured to travel along the protective sheath, the slidable member operatively coupled to the elongate member; wherein the elongate member is insertable into a lumen of a trans-dermal catheter by moving the slidable member along at least a part of the length of the protective sheath.

Abstract: A method and apparatus for repairing a damaged intervertebral disc nucleus in a minimally invasive manner utilizes a modular disc prosthesis preferably comprised of at least three modular segments and at least two rails that operably connect adjacent modular segments. In one embodiment, each modular segment includes a harder inner portion and a softer outer portion. Preferably, the rails operate to slidably connect and interlock adjacent modular segments. A stem portion of the rails that extends outside the periphery of the body of the prosthesis is removable after implantation such that the modular segments form an implanted unitary device that closely mimics the geometry of the disc nucleus cavity.

Abstract: A method and apparatus for repairing a damaged intervertebral disc nucleus in a minimally invasive manner utilizes a modular disc prosthesis preferably comprised of at least three modular segments and at least two rails that operably connect adjacent modular segments. In one embodiment, each modular segment includes a harder inner portion and a softer outer portion. Preferably, the rails operate to slidably connect and interlock adjacent modular segments. A stem portion of the rails that extends outside the periphery of the body of the prosthesis is removable after implantation such that the modular segments form an implanted unitary device that closely mimics the geometry of the disc nucleus cavity.

Abstract: A method and apparatus for repairing a damaged intervertebral disc nucleus in a minimally invasive manner utilizes a modular disc prosthesis preferably comprised of at least three modular segments and at least two rails that operably connect adjacent modular segments. In one embodiment, each modular segment includes a harder inner portion and a softer outer portion. Preferably, the rails operate to slidably connect and interlock adjacent modular segments. A stem portion of the rails that extends outside the periphery of the body of the prosthesis is removable after implantation such that the modular segments form an implanted unitary device that closely mimics the geometry of the disc nucleus cavity.

Abstract: A system and method for rejuvenating skin through ablation using a handheld device (200) having a removable treatment component (213) with an abrasive material on one surface of the component which surface is in a portion of the treatment component (213) configured to conform to a skin surface. The system further includes application of other elements to facilitate skin recovery and rejuvenation processes.

Abstract: A method and system for the creation or modification of the wear surface of orthopedic joints, involving the preparation and use of one or more partially or fully preformed and procured components, adapted for insertion and placement into the body and at the joint site. In a preferred embodiment, component(s) can be partially cured and generally formed ex vivo and further and further formed in vivo at the joint site to enhance conformance and improve long term performance. In another embodiment, a preformed balloon or composite material can be inserted into the joint site and filled with a flowable biomaterial in situ to conform to the joint site. In yet another embodiment, the preformed component(s) can be fully cured and formed ex vivo and optionally further fitted and secured at the joint site.

Abstract: An instrument for cutting an extension, such as a catheter or biomaterial, coupled to a prosthesis, such as a prosthesis located in an intervertebral disc space, that includes at least one axial member having a distal opening and at least one cutting device, such as for example a wire or blade, coupled to the at least one axial member that is capable of moving across at least a portion of the distal opening when a force is applied to the at least one cutting wire. A method for cutting a catheter is also disclosed. The removal instrument may be inserted into an introduction lumen. A force is applied to the at least one cutting device after the catheter is in the distal opening.

Abstract: The invention is a modular interbody fusion device for fusing adjacent spinal vertebrae that is adapted to be implanted in a prepared interbody space including a first modular segment having a width including a first rail extending at least partially along one side of the width and beyond a periphery of a body portion of the first modular segment, a second modular segment having a width and slidably connected to the first rail on one side of the width and having a second rail extending at least partially along another side of the width and beyond a periphery of a body portion of the second modular segment, a third modular segment having a width and slidably connected to the second rail on one side of the width and wherein the device has an expanded position in which the second and third modular segments are extended along the first and second rails and positioned in a generally end to end configuration spaced apart by the rails prior to implantation and an implanted position in which the modular segments are