BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Embolization Agent, Vascular

    PMA: P220020 · Supplement: S003 · Decision Sep 24, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2

    Basic Information

    Device Name
    Embolization Agent, Vascular
    Trade Name
    Lava Liquid Embolic System (Lava LES)
    PMA Number
    P220020
    Supplement Number
    S003
    Device Class
    FDA Class 3
    Product Code
    QVG
    Generic Name
    Embolization Agent, Vascular
    Medical Specialty
    Unknown
    Advisory Committee
    Cardiovascular
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    September 24, 2024
    Date Received
    August 28, 2024
    Supplement Type
    Special (Immediate Track)
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    update the Mixing Manifold assembly process by adding an additional inspection step

    Classifications

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

    Product Code Device Name
    QVG Embolization Agent, Vascular