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510(k) Data Aggregation

    K Number
    K172148
    Manufacturer
    Date Cleared
    2018-03-19

    (245 days)

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

    Anchorage Bone Plating System

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

    The Anchorage Bone Plating System is indication and fixation of fresh fractures, revision procedures, joint fusion, and reconstruction of small bones in the hands, feet, wrists, and toes. The system may be used in adults and pediatric patients.

    Device Description

    The Anchorage Bone Plating System includes single use bone fixation appliances intended to be permanently implanted. They are designed with different shape plates made from titanium alloy. The Anchorage Bone Plating System uses either a 3 mm or 3.5mm screws. The drill holes of the plates are aligned to assure the screws do not touch. The plates vary in curvature, length, thickness, number of holes, and plate shape. The Anchorage Bone Plating System is intended for fracture fixation.

    AI/ML Overview

    The provided text is a 510(k) summary for the Stryker Anchorage Bone Plating System. This document describes a medical device, its indications for use, and how it was determined to be substantially equivalent to a previously marketed device.

    Crucially, this document specifies:

    "Clinical testing was not required for this submission."

    Therefore, based solely on the provided text, there is no information available regarding a study that proves the device meets acceptance criteria related to clinical performance or AI/software algorithm performance. The substantial equivalence determination was based on non-clinical mechanical testing.

    As such, I cannot provide the requested information about acceptance criteria and a study proving the device meets them in the context of an AI/software algorithm.

    If this was a misunderstanding and you were expecting information about the mechanical acceptance criteria and how the non-clinical testing proved the device meets them, I can extract that to a limited extent:

    Information based on Non-Clinical Testing Section:

    • Acceptance Criteria (Implied): Mechanical performance equivalent to the predicate device, the Memometal Anchorage Bone Plating System (K083477).
    • Reported Device Performance: "Mechanical testing was performed and demonstrated that Stryker Anchorage Bone Plating System is equivalent in mechanical performance to the predicate device, the Memometal Anchorage Bone Plating System (K083477)."
    • Tests Performed:
      • Cantilever bending
      • Torque to failure
      • Push-Out
      • Shear-off

    However, the document does not provide any specific quantitative acceptance criteria values, sample sizes for these tests, or detailed results. It only states that equivalence was demonstrated.

    Therefore, I cannot fulfill your request for the comprehensive table and detailed study information as it pertains to AI/software performance or detailed quantitative mechanical performance data, because the provided text explicitly states "Clinical testing was not required for this submission" and does not describe such a study.

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