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

    Implant, Cochlear

    PMA: P970051 · Supplement: S125 · Decision Dec 12, 2014
    View on FDA
    Classifications
    1
    FEI Numbers
    22
    Registration Numbers
    22

    Basic Information

    Device Name
    Implant, Cochlear
    Trade Name
    NUCLEUS C1512 COCHLEAR IMPLANT SYSTEM
    PMA Number
    P970051
    Supplement Number
    S125
    Device Class
    FDA Class 3
    Product Code
    MCM
    Generic Name
    Implant, cochlear
    Medical Specialty
    Unknown
    Advisory Committee
    Ear, Nose, Throat
    Decision
    30-Day Notice Accepted
    Decision Code
    OK30
    Decision Date
    December 12, 2014
    Date Received
    November 12, 2014
    Supplement Type
    30-Day Notice
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    UPDATE THE ELECTRONIC ASSEMBLY INSPECTION STANDARD AND ALIGN THE ELECTRONIC ASSEMBLY INSPECTION STANDARD WITH THE CURRENT INSPECTION STANDARDS FOR THE NUCLEUS COCHLEAR IMPLANT SYSTEM.

    Classifications

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

    Product Code Device Name
    MCM Implant, Cochlear