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510(k) Data Aggregation

    K Number
    K081163
    Date Cleared
    2008-05-14

    (20 days)

    Product Code
    Regulation Number
    888.3027
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    SmartSet GMV Gentamicin Bone Cement is indicated for use in the second stage of a two-stage revision for total joint arthroplasty after the initial infection has been cleared.

    Device Description

    SmartSet GMV Gentamicin Bone Cement is a self-curing, radiopaque, polymethylmethacrylate based cement, containing the antibiotic gentamicin sulfate. The bone cement is used for securing a metal or polymeric prosthesis to living bone in arthroplasty procedures.

    AI/ML Overview

    The provided text is a 510(k) summary for a medical device (SmartSet GMV Gentamicin Bone Cement) and an FDA clearance letter. It is not a study report or a description of a study that establishes acceptance criteria and proves a device meets them in the context of an AI/ML medical device.

    Therefore, I cannot provide the requested information, particularly items 1-9, which are relevant to the evaluation of AI/ML performance.

    The document discusses:

    • Device Description: SmartSet GMV Gentamicin Bone Cement is a self-curing, radiopaque, polymethylmethacrylate based cement, containing the antibiotic gentamicin sulfate. It is used for securing a metal or polymeric prosthesis to living bone in arthroplasty procedures.
    • Intended Use/Indications For Use: It is indicated for use in the second stage of a two-stage revision for total joint arthroplasty after the initial infection has been cleared.
    • Substantial Equivalence: The primary basis for clearance is substantial equivalence to predicate devices (SmartSet GMV Endurance Gentamicin Bone Cement (K041656) and SmartSet GHV Gentamicin Bone Cement (K033563)), meaning its indications, intended use, formulation, and finished product specifications are equivalent.

    This type of submission relies on demonstrating similarity to already approved devices and often involves bench testing (physical and chemical properties) and biocompatibility testing, but not the kind of clinical performance or AI/ML evaluation implied by your detailed questions.

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