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510(k) Data Aggregation

    K Number
    K014194
    Manufacturer
    Date Cleared
    2002-01-17

    (27 days)

    Product Code
    Regulation Number
    888.3030
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The EBI® XFIX® Vision® Fixation System is a unilateral external fixation device intended for use in the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of the external fixation modality.

    Device Description

    The System consists of external fixation components and implantable bone screws. The EBI® XFIX® Vision® Fixation System is utilized in the following manner: bone screws are inserted through the patient's skin and soft tissue, and into the bone. The fixator frame of the EBI® XFIX® Vision® Fixation System is attached to the shanks of the bone screws. This submission is for the addition of "single locking" clamps to the existing System. The intended use and fundamental scientific technology have not changed from the previously cleared submission.

    AI/ML Overview

    The provided text is a 510(k) Summary for a medical device modification (EBI® XFIX® Vision® Fixation System) and the FDA's clearance letter. It focuses on demonstrating substantial equivalence to a predicate device rather than presenting a study with acceptance criteria for a new AI/software device.

    Therefore, the document does not contain the information required to populate the fields related to acceptance criteria, device performance, sample sizes, expert ground truth, adjudication methods, MRMC studies, standalone performance, or training set details.

    The document describes a modification to an existing external fixation system, specifically the addition of "single locking" clamps. The manufacturer asserts that the modified device is substantially equivalent to the predicate device in terms of intended use, materials, and function. This type of submission relies on demonstrating that the changes do not raise new questions of safety or effectiveness and that the modified device performs similarly to the already cleared predicate.

    No study proving the device meets acceptance criteria, as one would expect for an AI/software device, is described in this document. The basis for clearance is substantial equivalence to a predicate, not performance against specific metrics in a new study.

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