BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Aortic Valve, Prosthesis, Percutaneously Delivered

    PMA: P140031 · Supplement: S087 · Decision Jul 29, 2019
    View on FDA
    Classifications
    1
    FEI Numbers
    24
    Registration Numbers
    24

    Basic Information

    Device Name
    Aortic Valve, Prosthesis, Percutaneously Delivered
    Trade Name
    SAPIEN 3 and SAPIEN 3 Ultra Transcatheter Heart Valves
    PMA Number
    P140031
    Supplement Number
    S087
    Device Class
    FDA Class 3
    Product Code
    NPT
    Generic Name
    Aortic valve, prosthesis, percutaneously delivered
    Medical Specialty
    Unknown
    Advisory Committee
    Cardiovascular
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    July 29, 2019
    Date Received
    May 17, 2019
    Supplement Type
    Normal 180 Day Track
    Supplement Reason
    Labeling Change - Indications/instructions/shelf life/tradename
    Expedited Review
    N

    Advisory Committee Statement

    Approval for updates to the labeling of the SAPIEN 3 Transcatheter Heart Valve and Accessories and SAPIEN 3 Ultra Transcatheter Heart Valve and Accessories regarding additional valve-in-valve sizing guidance for implantation inside the Edwards INSPIRIS RESILIA aortic valve model 11500A.

    Classifications

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

    Product Code Device Name
    NPT Aortic Valve, Prosthesis, Percutaneously Delivered