BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Implant, Cochlear

    PMA: P000025 · Supplement: S004 · Decision Sep 4, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    22
    Registration Numbers
    22

    Basic Information

    Device Name
    Implant, Cochlear
    Trade Name
    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM
    PMA Number
    P000025
    Supplement Number
    S004
    Device Class
    FDA Class 3
    Product Code
    MCM
    Generic Name
    Implant, cochlear
    Medical Specialty
    Unknown
    Advisory Committee
    Ear, Nose, Throat
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    September 4, 2002
    Date Received
    August 20, 2002
    Supplement Type
    Real-Time Process
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR THE MODIFICATION TO REPLACE COMBI 40+ COCHLEAR IMPLANT SYSTEM "INSERTION ELECTRODE" WITH THE INSERTION TEST DEVICE (ITD). THE DEVICE, AS MODIFIED, WILL BE MARKETED UNDER THE TRADE NAME MED-EL INSERTION TEST DEVICE AND IS INDICATED FOR INDIVIDUALS UNDERGOING COCHLEAR IMPLANT SURGERIES AFTER A MASTOIDECTOMY, POSTERIOR TYMPANOTOMY, AND COCHLEOSTOMY HAVE BEEN PERFORMED AND WHERE ACCESS TO THE COCHLEA HAS BEEN SECURED.

    Classifications

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

    Product Code Device Name
    MCM Implant, Cochlear