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510(k) Data Aggregation

    K Number
    K041709
    Date Cleared
    2004-09-08

    (77 days)

    Product Code
    Regulation Number
    888.3030
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    NUMELOCK II SYSTEM

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

    The Numelock™ II System is intended for use in the temporary stabilization of long bone fractures.

    Device Description

    The Numelock™ II System consists of a series of locking plates and screws for the internal fixation of long bone fractures. The plates are available in different styles and configurations to fit various anatomical sites. Each plate has holes for screw fixation and is pre-contoured to fit the anatomical profile of the different periarticular regions of long bones.

    AI/ML Overview

    The provided document is a 510(k) premarket notification for the Numelock™ II System, a metallic bone fixation device. It describes the device and claims substantial equivalence to predicate devices, but it does not contain a study demonstrating that the device meets specific acceptance criteria related to numerical performance metrics.

    Therefore, I cannot populate the requested table and answer the study-related questions as the information is not present in the provided text.

    The document states:

    • "Mechanical testing demonstrated comparable mechanical properties to the predicate devices." This is a very high-level statement and does not provide specific acceptance criteria, reported performance values, or any details about the study (sample size, methodology, ground truth, etc.).

    In summary, the provided document does not contain the information required to answer your request about acceptance criteria and a study proving the device meets them.

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