BEUDAMED
    FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

    Implanted Fecal Incontinence Device

    PMA: P010020 · Supplement: S033 · Decision Jun 24, 2015
    View on FDA
    Classifications
    1
    FEI Numbers
    3
    Registration Numbers
    3

    Basic Information

    Device Name
    Implanted Fecal Incontinence Device
    Trade Name
    ACTICON NEOSPHINCTER ARTIFICIAL BOWEL SPHINCTER
    PMA Number
    P010020
    Supplement Number
    S033
    Device Class
    FDA Class 3
    Product Code
    MIP
    Generic Name
    Implanted fecal incontinence device
    Medical Specialty
    Unknown
    Advisory Committee
    Gastroenterology, Urology
    Decision
    30-Day Notice Accepted
    Decision Code
    OK30
    Decision Date
    June 24, 2015
    Date Received
    June 5, 2015
    Supplement Type
    30-Day Notice
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    QUALIFICATION OF THE LASER FIXTURE METHOD AS A REPLACEMENT FOR THE CURRENT CALIPER METHOD USED FOR MEASURING A CRITICAL TUBE DIMENSION.

    Classifications

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

    Product Code Device Name
    MIP Implanted Fecal Incontinence Device