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510(k) Data Aggregation

    K Number
    K131471
    Manufacturer
    Date Cleared
    2013-08-28

    (98 days)

    Product Code
    Regulation Number
    888.3040
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Self-Compressive Screws are intended for the fixation of bone fractures and for bone reconstruction in forefoot surgery.

    Device Description

    The Self-Compressive Screw consists of screws available in several diameters and lengths. All the implants are made of titanium alloy. The fixation is provided thanks to the threading of the screw, which allows compression.

    AI/ML Overview

    The provided document K131471 is a 510(k) summary for a medical device (Self-Compressive Screw). It explicitly states that no clinical studies were performed (Section VII, Page 3).

    Therefore, I cannot provide information on acceptance criteria, reported device performance, sample size, data provenance, expert details, adjudication methods, MRMC study results, or training set specifics, as these are typically associated with clinical performance evaluations.

    The document focuses on demonstrating substantial equivalence to a predicate device (Newclip Foot and Hand Motion System K091118) based on non-clinical mechanical tests:

    • Resistance to torsion according to ASTM F543 – Annex 1
    • Pull-out strength according to ASTM F543 Annex 3.

    The conclusion (Section VIII, Page 4) states that "NEOSTEO considers the current Self-Compressive Screw to be equivalent to the predicate device listed above. This conclusion is based on the devices' similarities in principles of operation, technology, materials and indications for use."

    Given the lack of clinical studies, the acceptance criteria and study details you requested are not available in this 510(k) submission.

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