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510(k) Data Aggregation

    K Number
    K041713
    Manufacturer
    Date Cleared
    2004-07-22

    (29 days)

    Product Code
    Regulation Number
    888.3040
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    SUPER REVO HERCULINE SUTURE ANCHOR

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

    The Super Revo® Herculine™ Suture Anchor is intended to be used for rotator cuff repairs in the shoulder either arthroscopically or in a mini-open technique.

    Device Description

    The Super Revo® Herculine™ Suture Anchor is a titanium suture anchor implant pre-threaded with undyed (white) and colored (white with blue stripe), nonabsorbable, braided, ultra-high molecular weight, polyethylene suture. It is provided preloaded onto a disposable driver with a stainless steel shaft and ABS handle. The Super Revo® Herculine™ Suture Anchor is supplied sterile and single use.

    The modification described in this Special 510(K) is to supply the Super Revo® suture anchor with the ultra-high molecular weight polyethylene suture.

    AI/ML Overview

    The provided text is a 510(k) summary for a medical device (Super Revo® Herculine™ Suture Anchor) and does not contain information about acceptance criteria or a study proving the device meets said criteria.

    The document states that the modification to the device (the type of suture used) "does not raise any new issues regarding safety and effectiveness" and that "Testing has been conducted to assure that providing the suture anchor with the ultra-high molecular weight, braided, polyethylene suture does not raise any new issues regarding safety and effectiveness." However, it does not provide details about what tests were conducted, their acceptance criteria, or the results.

    Therefore, I cannot provide a table of acceptance criteria and reported device performance or answer most of your specific questions. The document mainly focuses on demonstrating substantial equivalence to a predicate device rather than detailing specific performance studies with acceptance criteria.

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