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510(k) Data Aggregation

    K Number
    K061144
    Date Cleared
    2006-06-08

    (44 days)

    Product Code
    Regulation Number
    888.3027
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K053002, K041656, K033563, K053003, K053003

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

    Use in the second stage of a two-stage revision for total joint arthroplasty after the initial infection has been cleared.

    Device Description

    DePuy CMW 2 Gentamicin Bone Cement and DePuy CMW 3 Gentamicin Bone Cement are self-curing, polymethylmethacrylate (PMMA) bone cements containing the antibiotic gentamicin (at the rate of 1g active gentamicin in 40g of PMMA bone cement powder), for seating and securing of a metal or plastic prosthesis to living bone.

    AI/ML Overview

    The provided text is a 510(k) premarket notification summary for medical devices, specifically bone cements. It details the device's description, intended use, and claims of substantial equivalence to previously cleared predicate devices. It does not contain information related to acceptance criteria, device performance metrics, clinical study design (sample sizes, expert qualifications, etc.), or standalone algorithm performance.

    Therefore, I cannot fulfill your request for descriptions of acceptance criteria, device performance, or study details such as sample sizes, ground truth establishment, or multi-reader multi-case study results based on the provided text.

    The document primarily focuses on establishing substantial equivalence for regulatory clearance, not on reporting detailed performance metrics from a specific study against acceptance criteria.

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