BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    AdVance™ XP Male Sling System (720163-03)

    K Number: K242960 · Decision Nov 15, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    12
    Registration Numbers
    12
    Same Product Code
    11
    Applicant Total
    231
    Review Days
    51

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    Basic Information

    Device Name
    AdVance™ XP Male Sling System (720163-03)
    K Number
    K242960
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.3300
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Boston Scientific Corporation
    Date Received
    September 25, 2024
    Decision Date
    November 15, 2024
    Product Code
    OTM
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    GU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    OTM Mesh, Surgical, For Stress Urinary Incontinence, Male

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