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510(k) Data Aggregation

    K Number
    K042766
    Manufacturer
    Date Cleared
    2004-11-16

    (42 days)

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

    The Orthofix Volar Distal Radial Plate is intended for the volar fixation of fractures and osteotomies involving the distal radius.

    Device Description

    The Volar Distal Radial Plate is an anatomically contoured, Delta-shaped plate intended for volar applications to the distal radius. The Plate features an angled head with two rows of holes for placement of screws and non-threaded pegs that will be placed distally on the radius to secure bone fragments and provide stabilization. If a bone graft is required, framed access to the site is made possible by the triangular opening in the plate that spans from the plate head to the distal portion of the shaft. The shaft of the Plate is placed proximally on the distal radius and it offers a variety of K-wire and screw placement options for secure fixation to the external surface of the bone. The Plate provides the stabilization and fixation necessary in the treatment of distal radius fractures and osteotomies to allow early functional use of the hand.

    AI/ML Overview

    An acceptance criteria table and details on a study to prove a device meets acceptance criteria are typically found in the "Performance Data" or "Clinical Studies" sections of a 510(k) submission, neither of which are provided in the input text you've supplied.

    The provided text ("510(k) Summary of Safety and Effectiveness" for the "Orthofix Volar Distal Radial Plate") focuses on general device information, description, intended use, and substantial equivalence to predicate devices. It does not contain information regarding device performance, acceptance criteria, study details, sample sizes, expert qualifications, or ground truth establishment.

    Therefore, I cannot fulfill your request to describe the acceptance criteria and the study that proves the device meets them based on the provided text. The requested information is simply not present in this document.

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