BEUDAMED
    FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

    Iliac Covered Stent, Arterial

    PMA: P160021 · Supplement: S003 · Decision Aug 9, 2017
    View on FDA
    Classifications
    1
    FEI Numbers
    12
    Registration Numbers
    12

    Basic Information

    Device Name
    Iliac Covered Stent, Arterial
    Trade Name
    GoreViabahn VBX Balloon Expandable Endoprosthesis
    PMA Number
    P160021
    Supplement Number
    S003
    Device Class
    FDA Class 3
    Product Code
    PRL
    Generic Name
    Iliac covered stent, arterial
    Medical Specialty
    Unknown
    Advisory Committee
    Cardiovascular
    Decision
    30-Day Notice Accepted
    Decision Code
    OK30
    Decision Date
    August 9, 2017
    Date Received
    July 5, 2017
    Supplement Type
    30-Day Notice
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    Implementation of an automated deionized water fill station for use in the manufacturing of the GORE® VIABAHN® Endoprosthesis, GORE® TIGRIS® Vascular Stent and GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis.

    Classifications

    This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    PRL Iliac Covered Stent, Arterial