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510(k) Data Aggregation

    K Number
    K062863
    Manufacturer
    Date Cleared
    2006-10-31

    (36 days)

    Product Code
    Regulation Number
    888.3040
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    OSTEOMED EXTENDED 2.0/2.4CANNULATED SCREW SYSTEM

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

    The Osteomed Extended 2.0/2.4 Cannulated Screw System is indicated for bone fixation of hand and foot following trauma or osteotomy. Screws and washers are intended for single use only.

    Device Description

    The OsteoMed Extended 2.0/2.4 Cannulated Screw System is comprised of screws in diameters of 2.0mm (length 6mm to 42mm) to 2.4mm (length 6mm to 52mm). The screws are made from titanium alloy (ASTM F-136). Depth gauges, screwdrivers, drills, countersinks, k-wires, and preparation instruments will also be a part of the system.

    AI/ML Overview

    The provided text is a 510(k) summary and FDA clearance letter for a medical device, specifically the "OsteoMed Extended 2.0/2.4 Cannulated Screw System." This document is not a study report and therefore does not contain any information about acceptance criteria, device performance metrics (such as sensitivity, specificity, or AUC), sample sizes for test or training sets, ground truth establishment, or expert involvement for assessing AI or algorithmic performance.

    This device is a physical medical implant (bone screw system) and its clearance is based on substantial equivalence to previously marketed predicate devices, not on the performance of a software algorithm or AI.

    Therefore, I cannot provide the requested information. The document focuses on regulatory compliance, intended use, material composition, and design similarities to existing devices, rather than a clinical or technical performance study in the way an AI/software device would be evaluated.

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