BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Implant, Dermal, For Aesthetic Use

    PMA: P050033 · Supplement: S009 · Decision Aug 25, 2010
    View on FDA
    Classifications
    1
    FEI Numbers
    29
    Registration Numbers
    29

    Basic Information

    Device Name
    Implant, Dermal, For Aesthetic Use
    Trade Name
    HYDRELLE
    PMA Number
    P050033
    Supplement Number
    S009
    Device Class
    FDA Class 3
    Product Code
    LMH
    Generic Name
    Implant, dermal, for aesthetic use
    Medical Specialty
    Unknown
    Advisory Committee
    General, Plastic Surgery
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    August 25, 2010
    Date Received
    August 4, 2010
    Supplement Type
    Special (Immediate Track)
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR A QUALITY CONTROL TEST METHOD CHANGE FOR PROTEIN CONTENT DETERMINATION OF SODIUM HYALURONATE (NAHA) POWDER FROM THE CURRENT INTERNAL MODIFIED LOWRY TEST METHOD (TMS-219) TO THE MODIFIED LOWRY TEST METHOD IN THE EUROPEAN PHARMACOPOEIA (EP) SODIUM HYALURONATE MONOGRAPH.

    Classifications

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

    Product Code Device Name
    LMH Implant, Dermal, For Aesthetic Use