Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K992863
    Manufacturer
    Date Cleared
    1999-11-12

    (79 days)

    Product Code
    Regulation Number
    870.1380
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    LEAD STYLET,MODELS 6505,6506,6507,6508

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

    These stylets are wires intended to facilitate the placement of pacing leads during pacemaker implant procedures.

    The straight stylets are used to direct passage of a lead to the appropriate heart chamber and to wedge the lead in the trabeculae of the ventricle.

    The J-shaped stylets are used to direct passage of a lead in the atrium.

    Device Description

    The new accessory kits will allow separate packaging of lead stylets currently marketed with Guidant pace/sense and defibrillation leads. The stylets are provided in 0.014 and 0.016 inch diameters, with their respective "stiffness" labeled soft and firm. Each stylet package will contain two stylets of the same diameter. The stylets are made of chromium-nickel 304 stainless steel spring wire and have polypropylene Hercules PD 701 Knobs. The stylets are inserted into a coiled polyethylene stylet ring for packaging and ease of use purposes.

    AI/ML Overview

    This document is a 510(k) summary for the Accessory Stylet Kit. It explicitly states that no additional testing was deemed necessary because it concerns the separate packaging of currently marketed stylets. The document asserts that there are no changes to the design, materials, manufacturing process, packaging process, sterilization process, or shelf life of the subject device compared to previously cleared devices.

    Therefore, the requested information regarding acceptance criteria, study details, sample sizes, ground truth establishment, expert involvement, and comparative effectiveness studies is not applicable to this 510(k) submission. The substantial equivalence was established by demonstrating that the new accessory kits are identical in all relevant aspects to previously cleared stylets and accessory kits.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1