BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Acid, Hyaluronic, Intraarticular

    PMA: P950027 · Supplement: S001 · Decision Jul 8, 1997
    View on FDA
    Classifications
    1
    FEI Numbers
    21
    Registration Numbers
    21

    Basic Information

    Device Name
    Acid, Hyaluronic, Intraarticular
    Trade Name
    HYALGAN(R)
    PMA Number
    P950027
    Supplement Number
    S001
    Device Class
    FDA Class 3
    Product Code
    MOZ
    Generic Name
    Acid, hyaluronic, intraarticular
    Medical Specialty
    Unknown
    Advisory Committee
    Orthopedic
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    July 8, 1997
    Date Received
    June 24, 1997
    Supplement Type
    Normal 180 Day Track
    Supplement Reason
    Location Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR THE U.S. DISTRIBUTOR, SANOFI PHARMACEUTICALS, INC., NEW YORK, NEW YORK. ADDITIONALLY, WE HAVE REVIEWED THE EDITORIAL CHANGES YOU PROPOSE FOR THE LABELING FOR YOUR PRODUCT AND HAVE DETERMINED THAT THEY ARE APPROPRIATE.

    Classifications

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

    Product Code Device Name
    MOZ Acid, Hyaluronic, Intraarticular