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510(k) Data Aggregation

    K Number
    K211847
    Date Cleared
    2021-12-20

    (188 days)

    Product Code
    Regulation Number
    878.3300
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K121754

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The AdVance™ XP Male Sling System is intended for the treatment of male stress urinary incontinence (SUI) by the placement of a suburethral sling.

    Device Description

    AdVance™ XP Male Sling System is a sling system which treats male stress urinary incontinence by repositioning the urethra with a suburethral mesh. The AdVance XP Male Sling System is comprised of a permanently implanted monofilament polypropylene mesh sling, two needle passers used to implant the sling, and retraction system (retractor ring and stay hooks). The male sling is connected during the procedure to the needle passers through keved connectors at each end of the male sling which are removed after the male sling is positioned. The male sling reposition the bulbar urethra 2-4cms. The AdVance™ XP Male Sling System kit is composed of four primary components: Male Sling, Needle Passers, Retractor Ring, and Stay Hooks. The AdVance™ XP Male Sling and Needle Passers are the subject of this submission. The Retraction System (retractor ring and stay hooks) is purchased pre-sterilized off the shelf components and is cleared through K791665.

    AI/ML Overview

    The provided text is a 510(k) summary for a medical device (AdVance™ XP Male Sling System). It details the device's characteristics, comparison to a predicate device, and various performance tests. However, it does not include information about acceptance criteria or a study proving the device meets acceptance criteria related to an AI/ML device, as requested in the prompt. The device described here is a physical surgical implant, not an AI/ML system.

    Therefore, I cannot extract the requested information regarding acceptance criteria and study details for an AI/ML device from this document.

    The document discusses:

    • Acceptance Criteria for the physical device: Primarily demonstrated through bench testing, sterilization evaluation, and shelf life testing, showing comparability to the predicate device in terms of technological characteristics and performance.
    • Device Performance: Stated that "performance testing demonstrate that the technological characteristics and performance criteria of the AdVance™ XP Male Sling System are comparable to the predicate device (K182169) and functions as intended equivalent to devices currently on the market for the same intended use."

    But none of the specific AI/ML-related questions (e.g., sample sizes for test/training sets, expert ground truth, MRMC study, standalone performance) can be answered from this content.

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