Abstract: Motion control integration including: a centralized integration system including data storage, a user interface, and multiple network connections; a first motion platform connected to the centralized integration system; a second motion platform connected to the centralized integration system; and a shared clock, where the centralized integration system shares clock data with the first motion platform and the second motion platform.

Abstract: Illuminated top furniture including an illuminated top portion and a support portion. The illuminated top portion includes a support layer, at least one light source, a light diffusion layer and an upper protective layer. The at least one light source is mounted to the support layer. The light diffusion layer is positioned on a side of the at least one light source that is opposite the support layer. The upper protective layer is positioned on a side of the light diffusion layer that is opposite the support layer. At least a portion of the upper protective layer is transparent such that light emitted by the at least one light source is visible through the upper protective layer while the light diffusion layer obscures the at least one light source so that the at least one light source is not visible through the upper protective layer. The support portion is attached to the illuminated top portion to support the illuminated top portion above a ground surface.

Abstract: Illuminated top furniture including an illuminated top portion and a support portion. The illuminated top portion includes a support layer, at least one light source, a light diffusion layer and an upper protective layer. The at least one light source is mounted to the support layer. The light diffusion layer is positioned on a side of the at least one light source that is opposite the support layer. The upper protective layer is positioned on a side of the light diffusion layer that is opposite the support layer. At least a portion of the upper protective layer is transparent such that light emitted by the at least one light source is visible through the upper protective layer while the light diffusion layer obscures the at least one light source so that the at least one light source is not visible through the upper protective layer. The support portion is attached to the illuminated top portion to support the illuminated top portion above a ground surface.

Abstract: A minimally invasive dilation device includes a plurality of rigid arms radially arrayed about a center and a dilating member positioned between the arms. A stylus may occupy the center. An outer flexible sleeve may be circumferentially secured to the arms, lying within or without the plurality of arms. An inner mesh may surround the stylus and dilating member. The device may be introduced into tissue toward a targeted area, while in a closed configuration. The dilating member may be a balloon, wherein upon inflation of the balloon, the arms are pushed radially outward, expanding the device and dilating the surrounding tissue. The dilating member may be a tube, wherein upon insertion of the tube, the arms are pushed radially outward. A cannula may be inserted inside the plurality of arms to keep the arms in an open configuration, and the dilating member may be withdrawn, providing an open passageway through the device to the targeted area. The device may be used with a neural monitoring system.

Abstract: A minimally invasive dilation device includes a plurality of rigid arms radially arrayed about a center and a dilating member positioned between the arms. A stylus may occupy the center. An outer flexible sleeve may be circumferentially secured to the arms, lying within or without the plurality of arms. An inner mesh may surround the stylus and dilating member. The device may be introduced into tissue toward a targeted area, while in a closed configuration. The dilating member may be a balloon, wherein upon inflation of the balloon, the arms are pushed radially outward, expanding the device and dilating the surrounding tissue. The dilating member may be a tube, wherein upon insertion of the tube, the arms are pushed radially outward. A cannula may be inserted inside the plurality of arms to keep the arms in an open configuration, and the dilating member may be withdrawn, providing an open passageway through the device to the targeted area. The device may be used with a neural monitoring system.

Abstract: A minimally invasive dilation device includes a plurality of rigid arms radially arrayed about a center and a dilating member positioned between the arms. A stylus may occupy the center. An outer flexible sleeve may be circumferentially secured to the arms, lying within or without the plurality of arms. An inner mesh may surround the stylus and dilating member. The device may be introduced into tissue toward a targeted area, while in a closed configuration. The dilating member may be a balloon, wherein upon inflation of the balloon, the arms are pushed radially outward, expanding the device and dilating the surrounding tissue. The dilating member may be a tube, wherein upon insertion of the tube, the arms are pushed radially outward. A cannula may be inserted inside the plurality of arms to keep the arms in an open configuration, and the dilating member may be withdrawn, providing an open passageway through the device to the targeted area. The device may be used with a neural monitoring system.

Abstract: A minimally invasive dilation device includes a plurality of rigid arms radially arrayed about a center and a dilating member positioned between the arms. A stylus may occupy the center. An outer flexible sleeve may be circumferentially secured to the arms, lying within or without the plurality of arms. An inner mesh may surround the stylus and dilating member. The device may be introduced into tissue toward a targeted area, while in a closed configuration. The dilating member may be a balloon, wherein upon inflation of the balloon, the arms are pushed radially outward, expanding the device and dilating the surrounding tissue. The dilating member may be a tube, wherein upon insertion of the tube, the arms are pushed radially outward. A cannula may be inserted inside the plurality of arms to keep the arms in an open configuration, and the dilating member may be withdrawn, providing an open passageway through the device to the targeted area. The device may be used with a neural monitoring system.

Abstract: A packaging system includes a bottle defining two separate closed compartments for separately carrying a consumable liquid and a solid. Liquid is held in the first compartment by a cap, and a solid (such as medication, pill, or other solid) is held in the second compartment by a closure member such as a sheet or film. The system facilitates injections of the solid by providing sufficient liquid to permit swallowing the solid. A related method includes storing two related products, one solid and one liquid, in a single container so that a user can use one of the products to facilitate injections of the other.

Abstract: Apparatus, systems, and methods for spine surgery employ a guide wire temporarily anchored to a contralateral side of an intervertebral disc. The guide wire establishes a reliable pathway for passage and actuation of cannulated instruments or implants through a small working channel leading to an ipsilateral side of the disc. The guide wire may be disconnected and removed from the disc after use.

Abstract: A system for single tunnel, double bundle anterior cruciate ligament reconstruction includes implant constructs and instruments. The implant constructs provide a combination of cortical fixation and bone tunnel aperture fixation. The implant constructs separate a graft into distinct bundles. The instruments are used to prepare shaped bone tunnels to receive the implant constructs and graft bundles. Methods for reconstructing the antero-medial and postero-lateral bundles of the anterior cruciate ligament may rely on single femoral and tibial tunnels and a single strand of graft.

Abstract: A system for single tunnel, double bundle anterior cruciate ligament reconstruction includes implant constructs and instruments. The implant constructs provide a combination of cortical fixation and bone tunnel aperture fixation. The implant constructs separate a graft into distinct bundles. The instruments are used to prepare shaped bone tunnels to receive the implant constructs and graft bundles. Methods for reconstructing the antero-medial and postero-lateral bundles of the anterior cruciate ligament may rely on single femoral and tibial tunnels and a single strand of graft.

Abstract: A system and method for securing an ACL graftmay include a line routed through a plate. The plate may include an elongated body with a plurality of passageways, and a dogbone feature on at least one end of the body. The line may be routed to create at least one one-way slide so no knots are required. The line may form an adjustable loop that receives the graft. The adjustable loop is adjustable through the one-way slide feature. The plate may be configured to pass through a bone tunnel. The plate may be toggled after passage through the bone tunnel to prevent withdrawal back through the bone tunnel because the plate contact area is larger the bone tunnel area.

Abstract: Apparatus, systems, and methods for spine surgery employ a guide wire temporarily anchored to a contralateral side of an intervertebral disc. The guide wire establishes a reliable pathway for passage and actuation of cannulated instruments or implants through a small working channel leading to an ipsilateral side of the disc. The guide wire may be disconnected and removed from the disc after use.

Abstract: A minimally invasive dilation device includes a plurality of rigid arms radially arrayed about a center and a dilating member positioned between the arms. A stylus may occupy the center. An outer flexible sleeve may be circumferentially secured to the arms, lying within or without the plurality of arms. An inner mesh may surround the stylus and dilating member. The device may be introduced into tissue toward a targeted area, while in a closed configuration. The dilating member may be a balloon, wherein upon inflation of the balloon, the arms are pushed radially outward, expanding the device and dilating the surrounding tissue. The dilating member may be a tube, wherein upon insertion of the tube, the arms are pushed radially outward. A cannula may be inserted inside the plurality of arms to keep the arms in an open configuration, and the dilating member may be withdrawn, providing an open passageway through the device to the targeted area. The device may be used with a neural monitoring system.