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510(k) Data Aggregation

    K Number
    K042947
    Manufacturer
    Date Cleared
    2004-12-27

    (62 days)

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

    PARALLAX ACRYLIC RESIN WITH TRACERS, MODEL KP-PAR-003

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

    Parallax® Acrylic Resin with TRACERS® is indicated for the fixation of pathological fractures of the vertebral body using vertebroplasty or kyphoplasty procedures. Painful vertebral compression fractures may result from osteoporosis, benign lesions (hemangioma), and malignant lesions (metastatic cancers, myleoma).

    Device Description

    Parallax® Acrylic Resin with TRACERS® is an opacified polymethylmethacrylate bone cement.

    AI/ML Overview

    The provided text is a 510(k) summary for the ArthroCare Corporation Parallax® Acrylic Resin with TRACERS® bone cement, and it primarily focuses on establishing substantial equivalence to a predicate device. It does not contain information about the performance criteria, a detailed study with specific acceptance criteria, or the types of information requested in the prompt (e.g., sample sizes for test/training sets, expert qualifications, HRMR studies, etc.).

    Instead, the document asserts substantial equivalence based on:

    • Indications for Use
    • Materials
    • Mechanical properties
    • Performance testing (details not provided)

    Therefore, I cannot extract the requested information from the provided text. The document states "performance testing has been completed to demonstrate the substantial equivalence," but it does not describe the specific acceptance criteria, test methodology, or results in a way that would allow me to populate the requested table or answer the specific questions about study design elements.

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