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510(k) Data Aggregation

    K Number
    K203773

    Validate with FDA (Live)

    Device Name
    BRM TOOL Screws
    Date Cleared
    2022-01-14

    (387 days)

    Product Code
    Regulation Number
    888.3040
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The BRM TOOL Screws are indicated for use for aligned bone fracture repair and arthrodesis, osteotomy, joint fusion and bone fragment fixation appropriate with the size of the screw.

    Device Description

    The BRM TOOL Screws are interfragmentary compression osteosynthesis screws, i.e., devices used in surgical orthopedic interventions to provide support to the bone, ligament, tendon or cartilage structure, with the aim to reduce fractures in several parts of the skeleton, particularly of bone epiphyses. The application field excludes spinal, rib cage and skull bones. The BRM TOOL Screws are available in Titanium alloy.

    AI/ML Overview

    The provided document is a 510(k) summary for the BRM TOOL Screws, a medical device for bone fixation. It describes the device, its intended use, and its substantial equivalence to predicate devices, but it does not contain information about an AI/ML device or a study involving human readers or AI assistance.

    Therefore, I cannot provide the requested information regarding acceptance criteria and performance of an AI/ML device because the document does not describe such a device or study.

    The document discusses mechanical testing of the screws (torsional yield strength, driving torque, and pullout strength) and mentions that results met predefined acceptance criteria per ASTM F543 and ASTM F1264, and LAL testing, but this relates to the physical characteristics of the screws, not an AI/ML system.

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