BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Stent, Coronary

    PMA: P020047 · Supplement: S001 · Decision Oct 8, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    28
    Registration Numbers
    28

    Basic Information

    Device Name
    Stent, Coronary
    Trade Name
    MULTI-LINK RX AND OTW VISION CORONARY STENT SYSTEMS
    PMA Number
    P020047
    Supplement Number
    S001
    Device Class
    FDA Class 3
    Product Code
    MAF
    Generic Name
    STENT, CORONARY
    Medical Specialty
    Unknown
    Advisory Committee
    Cardiovascular
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    October 8, 2003
    Date Received
    October 2, 2003
    Supplement Type
    Special (Immediate Track)
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR THE ADDITION OF A TEMPORARY, POST-STERILE SAMPLING INSPECTION PLAN FOR THE SMALL (3.0 MM DIAMETER) MULTI-LINK VISION CORONARY STENT SYSTEM.

    Classifications

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

    Product Code Device Name
    MAF Stent, Coronary