BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Implant, Dermal, For Aesthetic Use

    PMA: P050047 · Supplement: S019 · Decision Sep 23, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    29
    Registration Numbers
    29

    Basic Information

    Device Name
    Implant, Dermal, For Aesthetic Use
    Trade Name
    JUVEDERM HYALURONATE GEL IMPKANTS
    PMA Number
    P050047
    Supplement Number
    S019
    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
    September 23, 2011
    Date Received
    August 1, 2011
    Supplement Type
    Real-Time Process
    Supplement Reason
    Labeling Change - Indications/instructions/shelf life/tradename
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR AN EXTENSION OF THE SHELF LIFE FROM 12 MONTHS TO 24 MONTHS FOR THE 0.8ML SYRINGE (0.4ML AND 0.8ML VOLUMES); AN INCREASE IN THE MONOETHYLGLYCINEXYIDIDE (MEGX) IMPURITY SPECIFICATION FROM <= 0.3% W/W OF LABEL STRENGTH TO <= 2.0% W/W OF LABEL STRENGTH; AND AN INCREASE IN TOTAL IMPURITIES SPECIFICATION FROM <= 0.5% W/W OF LABEL STRENGTH TO <= 2.5% W/W OF LABEL STRENGTH.

    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