Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K122334
    Date Cleared
    2012-11-28

    (118 days)

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

    The CheckMate™ Small Bone Fusion System is intended for the treatment of fracture fixation, osteotomies (ex. Akin, Chevron, Scarf, Weil), reconstruction, revision surgery and arthrodesis of small bones in the upper and lower extremities.

    Device Description

    The CheckMate™ Small Bone Fusion System consists of 2-hole bone plates made available in three length options, and 2.0 mm and 2.7 mm diameter bone screws having lengths varying from 8 mm to 24 mm. The bone plate is pre-assembled with a suture . loop intended to provide a traction force required to achieve compression between bone segments. The bone screws have a snap-off feature designed to work with the plates and/or as standalone bone fixation fasteners. The bone plates and screws are manufactured from implant grade stainless steel.

    AI/ML Overview

    The provided document is a 510(k) summary for the CheckMate™ Small Bone Fusion System. It states the intended use, device description, and substantial equivalency to predicate devices. However, this document does not contain information about studies to prove specific acceptance criteria for device performance based on clinical outcomes, AI performance metrics, or ground truth establishment relevant to the questions asked.

    Therefore, I cannot fulfill the request as the necessary information regarding acceptance criteria, study details, sample sizes, expert qualifications, adjudication methods, MRMC studies, standalone AI performance, or training set ground truth is not present in the provided text.

    The document focuses on regulatory approval through substantial equivalence, which relies on demonstrating similarity to already cleared devices based on intended use, materials, and design, typically supported by comparative mechanical testing (e.g., four-point bending tests) and dimensional analyses, rather than clinical efficacy studies.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1