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510(k) Data Aggregation

    K Number
    K082922
    Date Cleared
    2008-12-09

    (69 days)

    Product Code
    Regulation Number
    870.1330
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    FREEWAY AND RAILRUNNER GUIDEWIRES

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

    For use in Angiographic procedures to introduce and position catheters and interventional devices within the coronary and peripheral vasculature.

    Device Description

    These Freeway™ and Railrunner™ Guidewires are composed of two primary components: A PTFE coated stainless steel steerable core body, and a radiopaque platinum alloy distal coil. The coil is secured in its location by solder, which is attached to the core. The coil is attached to the core at the distal end, proximal end of the coil, and at a midpoint section (intermediate ioint). The product is offered with a shapeable straight tip or in a pre-shaped configuration. The Guidewires are optionally coated with MDX (silicone) over the distal tip and hydrophilic coating over portions of the distal tip of the Guidewire. The Guidewires are bound by the following parameters: Outside Diameter: .014", Lengths: 175cm - 300 cm, Tips: Straight or shaped, Flexibility: FREEWAY - 3 and 6 gm and RAILRUNNER - 9 and 12 gm distal loads.

    AI/ML Overview

    No AI device assessment was conducted in the provided document. The submission is for Freeway™ and Railrunner™ Guidewires, which are physical medical devices (guidewires) and not an AI/ML software. Therefore, the requested information about acceptance criteria, study details, and AI performance metrics is not applicable based on the given text.

    The document discusses non-clinical testing to demonstrate equivalence to predicate devices, biocompatibility testing, and conformance with design control procedures and quality systems, but these do not involve AI performance evaluation.

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