Search Filters

Search Results

Found 3 results

510(k) Data Aggregation

    K Number
    K160076
    Device Name
    XCage™ Interbody Fusion System
    Manufacturer
    Ouroboros Medical, Inc.
    Date Cleared
    2016-10-13

    (273 days)

    Product Code
    MAX
    Regulation Number
    888.3080
    Why did this record match?
    Applicant Name (Manufacturer) :

    Ouroboros Medical, Inc

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The XCage™ Interbody Fusion System is indicated for spinal intervertebral body fusion with autogenous bone graft in skeletally mature individuals with degenerative disc disease (DDD) at one or two contiguous levels from L2 to S1, following discectomy. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have at least six (6) months of non-operative treatment. Additionally, these patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). XCage™ System Spacers are intended to be used with supplemental fixation instrumentation, which has been cleared for use in the lumbar spine.
    Device Description
    The Ouroboros XCage™ Interbody Fusion System is an expandable lumbar intervertebral body fusion device intended for use in the lumbosacral spine from L2 to S1 and is intended for intervertebral lumbar fusion. The XCage™ Spacer consists of a Shell and a Shim component that are offered in a range of sizes to accommodate variation in patient anatomy. The Shell component is a rectangular frame with struts on all four sides that allow for insertion into the intervertebral body space in a non-expanded form, and subsequent expansion following the insertion of the Shim component. The Shim component has a tapered front end that inserts into and expands the Shell component to the desired vertical and horizontal dimensions. When fully inserted, the Shim locks within the Shell to provide structural stability for interbody fusion. An integrated "Core" in the Shell serves to anchor the delivery instrument during Shim insertion. Protrusions on the superior and inferior surfaces of the Spacer grip the adjacent vertebral endplates to resist expulsion. The XCage™ Spacer is to be filled with autogenous bone graft material. Once implanted, the XCage™ Spacer is designed to restore intervertebral disc height, provide anterior column support and maintain structural stability of the motion segment to facilitate intervertebral body fusion. The XCage Interbody Fusion System includes: - 1. The spacer components: shell and shim - 2. A set of re-useable manual surgical instruments for delivery of the device - 3. 23 mm and 27 mm implant lengths - 4. 0 and 6 degrees lordotic angles on the implant The XCage™ shell is made from polyetheretherketone (PEEK) per ASTM F2026, and integrated tantalum radiographic markers per ASTM F560. The XCage™ Shim and Core are made from Titanium alloy per ASTM F136. The re-usable surgical instruments are made from stainless steel.
    Ask a Question
    K Number
    K133514
    Device Name
    XCAGE INTERBODY FUSION SYSTEM
    Manufacturer
    OUROBOROS MEDICAL
    Date Cleared
    2014-05-01

    (167 days)

    Product Code
    MAX
    Regulation Number
    888.3080
    Why did this record match?
    Applicant Name (Manufacturer) :

    OUROBOROS MEDICAL

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The XCage™ Interbody Fusion System is indicated for spinal intervertebral body fusion with autogenous bone graft in skeletally mature individuals with degenerative disc disease (DDD) at one or two contiguous levels from L2 to S1, following discectomy. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have at least six (6) months of non-operative treatment. Additionally, these patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). XCage™ system Spacers are intended to be used with supplemental fixation instrumentation, which has been cleared for use in the lumbar spine.
    Device Description
    The Ouroboros XCage™ Interbody Fusion System is an expandable lumbar intervertebral body fusion device intended for use in the lumbosacral spine from L2 to S1 and is intended for intervertebral lumbar fusion. The XCage™ Spacer consists of a Shell and a Shim component that are offered in a range of sizes to accommodate variation in patient anatomy. The Shell component is a rectangular frame with struts on all four sides that allow for insertion into the intervertebral body space in a nonexpanded form, and subsequent expansion following the insertion of the Shim component. The Shim component has a tapered front end that inserts into and expands the Shell component to the desired vertical and horizontal dimensions. When fully inserted, the Shim locks within the Shell to provide structural stability for interbody fusion. An integrated "Core" in the Shell serves to anchor the delivery instrument during Shim insertion. Protrusions on the superior and inferior surfaces of the Spacer grip the adjacent vertebral endplates to resist expulsion. The XCage™ Spacer is to be filled with autogenous bone graft material. Once implanted, the XCage™ Spacer is designed to restore intervertebral disc height, provide anterior column support and maintain structural stability of the motion segment to facilitate intervertebral body fusion. The Ouroboros XCage™ Shell is manufactured from polyetheretherketone (PEEK) per ASTM F2026, and has integrated tantalum radiographic markers per ASTM F560. The XCageTM Shim and Core are made from Titanium alloy per ASTM F136. The Ouroboros XCage™ Interbody Fusion System includes a set of re-useable manual surgical instruments for delivery of the device.
    Ask a Question
    K Number
    K122861
    Device Name
    XTOOL
    Manufacturer
    OUROBOROS MEDICAL
    Date Cleared
    2012-12-07

    (80 days)

    Product Code
    HRX
    Regulation Number
    888.1100
    Why did this record match?
    Applicant Name (Manufacturer) :

    OUROBOROS MEDICAL

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The XTool™ Device is indicated for spinal discectomy procedures for the cutting and removal of soft and hard tissue in open and minimally invasive spinal surgeries.
    Device Description
    The XTool™ is an orthopedic manual hand held surgical instrument for use in performing discectomy in open and minimally invasive spine procedures. It is composed of an angled cutting head with serrated cutting edges and a distal guard, and a hollow shaft that connects the cutting head to the handle proximal. The handle has a port for connecting to standard hospital wall or pump suction. Two different diameter devices are specified to accommodate the range of disc heights for which a discectomy can be performed, with the smaller diameter for lower height discs, and the larger diameter for larger height disc. Two different tip angles are also specified to facilitate ipsilateral and contralateral disc removal. The finished assembly working length is 22 cm, Tip Angle is 15° or 40° and the cutter head diameter is either 5.2 mm or 6.3 mm.
    Ask a Question

    Page 1 of 1