BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Implant, Cochlear

    PMA: P940022 · Supplement: S021 · Decision Jun 6, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    22
    Registration Numbers
    22

    Basic Information

    Device Name
    Implant, Cochlear
    Trade Name
    BTE (BEHIND-THE-EAR) SYSTEM SENSOR (ADULT)
    PMA Number
    P940022
    Supplement Number
    S021
    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
    June 6, 2002
    Date Received
    May 28, 2002
    Supplement Type
    Real-Time Process
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR THE BTE SYSTEM SENSOR, AN ACCESSORY ITEM TO BE OFFERED FOR USE WITH THE BTE SOUND PROCESSOR FOR LIMITED VERIFICATION OF SYSTEM FUNCTIONALITY.

    Classifications

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

    Product Code Device Name
    MCM Implant, Cochlear