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510(k) Data Aggregation

    K Number
    K020554
    Date Cleared
    2002-05-03

    (72 days)

    Product Code
    Regulation Number
    888.3800
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K961051

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

    Indicated for intractable pain resulting from traumatic arthritis, rheumatoid arthritis, trauma-induced osteoarthritis of the radial/carpal joint. To replace functionality of the joint due to deformity or elements stated above. Intended for cemented use only.

    Device Description

    The KMI Universal Total Wrist™ (UTW) System (either predicate or modification) consists of the following components: the radial implant, the carpal plate implant, the carpal polymer component and two bone screws. The system is offered in three sizes (small, medium, and large), with three matching polymer component sizes, which are available in varying thicknesses (standard, +1 mm, +2 mm). It is constructed of materials that have a long clinical history of proven acceptance and performance. This system is intended for use with cement and will be promoted as such in the UTW surgical technique manual.

    AI/ML Overview

    The provided text is a 510(k) summary for a medical device (Universal Total Wrist™ System), not a study report detailing acceptance criteria and performance against those criteria. Therefore, I cannot extract the requested information as it is not present in the provided document.

    The document focuses on:

    • Administrative information: Manufacturer, contact, device names, predicate device.
    • Intended use: Medical conditions for which the device is indicated.
    • System description: Components, sizes, and materials.
    • Equivalence to marketed product: Claims of similarity to a predicate device.
    • FDA clearance letter: Confirmation of substantial equivalence.
    • Indications for Use statement: Formal statement of approved uses.

    There is no mention of:

    • Specific acceptance criteria (numerical thresholds for performance).
    • A study proving the device meets acceptance criteria.
    • Sample sizes for test or training sets.
    • Data provenance, expert qualifications, or adjudication methods for ground truth establishment.
    • Comparative effectiveness studies (MRMC) or standalone algorithm performance.

    The document describes a modification to an existing device, emphasizing its substantial equivalence to the predicate device based on material composition, intended use, operating principle, and basic design, rather than presenting a performance study with detailed acceptance criteria.

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