BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Implant, Dermal, For Aesthetic Use

    PMA: P800022 · Supplement: S052 · Decision May 11, 2004
    View on FDA
    Classifications
    1
    FEI Numbers
    29
    Registration Numbers
    29

    Basic Information

    Device Name
    Implant, Dermal, For Aesthetic Use
    Trade Name
    COSMODERM AND COSMOPLAST HUMAN-BASED COLLAGEN
    PMA Number
    P800022
    Supplement Number
    S052
    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
    May 11, 2004
    Date Received
    October 24, 2003
    Supplement Type
    Normal 180 Day Track
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR A NEW RAW MATERIAL SUPPLIER FOR THE HUMAN COLLAGEN COMPONENT OF COSMODERM AND COSMOPLAST (I.E., IMMUCOR/GAMMA BIOLOGICALS OF HOUSTON, TEXAS).

    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