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510(k) Data Aggregation

    K Number
    K182361

    Validate with FDA (Live)

    Manufacturer
    Date Cleared
    2018-12-18

    (110 days)

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

    The Arthrex Compression FT Screws are intended for fixation of small bone fragments, such as apical fragments, osteochondral fragments and cancellous fragments. Specific applications include the following:

    • . Osteochondral fragments (talar vault, femoral condyle)
    • . apical fragments (radial head, patellar rim, navicular, metacarpal/metatarsal)
    • . cancellous fragments (talus)
    • o Carpal, metacarpal, and small hand bone
    • . tarsal and metatarsals
    • . phalanges
    • . Intra-articular fractures
    • o ankle
    • . proximal and distal humerus
    • . proximal and distal radius
    • . proximal and distal ulna
    • . osteocondral fixation and fractures
    • Osteochondritis Dissecans .
    • . Fixation of fractures and osteotomies about the knee
    • Oblique fractures of the fibula .
    • . Reconstructive surgeries of the foot
    • . malleolar fixation
    Device Description

    The Arthrex Compression FT Screws are a family of titanium, cannulated, compression screws that are offered in a diameter range of 2.5 to 4.0mm, length range of 32 to 60mm, in a fully threaded design.

    AI/ML Overview

    The provided text is a 510(k) summary for the Arthrex Compression FT Screws. It describes the device, its intended use, and its equivalence to predicate devices, but does not contain information related to the acceptance criteria of a study, the study itself, or its results in the context of device performance metrics often associated with AI/ML devices.

    The document states that "Push-out, torque and compression testing were conducted to demonstrate that the proposed longer Arthrex Compression FT Screws perform statistically equivalent to the predicate." However, it does not provide:

    • A table of acceptance criteria and the reported device performance.
    • Sample size used for the test set and data provenance.
    • Number of experts used to establish ground truth or their qualifications.
    • Adjudication method.
    • Multi-reader multi-case (MRMC) comparative effectiveness study data or effect size.
    • Standalone algorithm performance data.
    • Type of ground truth used.
    • Sample size for the training set.
    • How ground truth for the training set was established.

    This type of information is typically found in submissions for devices that incorporate AI/Machine Learning, which this traditional orthopedic fixation device does not. The 510(k) for the Arthrex Compression FT Screws focuses on demonstrating substantial equivalence through engineering and biomechanical testing against predicate devices.

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