BEUDAMED
    FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

    EXAIR ANTERIOR AND POSTERIOR PROLAPSE REPAIR SYSTEMS

    K Number: K083499 · Decision May 8, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    4
    Registration Numbers
    4
    Same Product Code
    30
    Applicant Total
    71
    Review Days
    164

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    Basic Information

    Device Name
    EXAIR ANTERIOR AND POSTERIOR PROLAPSE REPAIR SYSTEMS
    K Number
    K083499
    Device Class
    FDA class 3
    Clearance Type
    Traditional
    Regulation Number
    884.5980
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Coloplast A/S
    Date Received
    November 25, 2008
    Decision Date
    May 8, 2009
    Product Code
    OTP
    Advisory Committee
    Obstetrics/Gynecology
    Review Advisory Committee
    OB
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    OTP Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed

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