BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Intracranial Coil-Assist Stent

    PMA: P170013 · Supplement: S006 · Decision Jul 16, 2021
    View on FDA
    Classifications
    1
    FEI Numbers
    6
    Registration Numbers
    6

    Basic Information

    Device Name
    Intracranial Coil-Assist Stent
    Trade Name
    Low-Profile Visualized Intraluminal Support (LVIS) and LVIS Jr.
    PMA Number
    P170013
    Supplement Number
    S006
    Device Class
    FDA Class 3
    Product Code
    QCA
    Generic Name
    Intracranial coil-assist stent
    Medical Specialty
    Unknown
    Advisory Committee
    Neurology
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    July 16, 2021
    Date Received
    April 23, 2021
    Supplement Type
    Real-Time Process
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    Approval for the change in antioxidants used in the dispenser hoop of packaging of the Flow Re-Direction Endoluminal Device (FRED) System, Woven EndoBridge (WEB) Aneurysm Embolization System and Low-Profile Visualized Intraluminal Support (LVIS) and LVIS Jr. devices.

    Classifications

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

    Product Code Device Name
    QCA Intracranial Coil-Assist Stent