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510(k) Data Aggregation

    K Number
    K091918
    Manufacturer
    Date Cleared
    2009-10-07

    (99 days)

    Product Code
    Regulation Number
    892.1650
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    ZEN-2090 PRO, FLUOROSCOPIC X-RAY SYSTEM, MODEL ZEN-2090 PRO

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

    ZEN-2090 Pro is a mobile digital C-arm designed to provide fluoroscopic and radiographic images of the patient during diagnostic, surgical and interventional procedures. Examples of clinical application may include cholangiography, endoscopy, orthopedic, neurologic, stone localization, critical care and emergency room procedures i.e. surgical interventions needing X-ray imaging and/or guidance and interventions inside and outside the operating room.

    Device Description

    ZEN-2090 Pro is consisted of the X-ray tube, X-ray tube assembly, x-ray controller, XTV camera and some accessories. The ZEN-2090 Pro is a device intended to visualize anatomical structures by converting a pattern of x-radiation into a visible image through electronic amplification. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

    AI/ML Overview

    The provided text describes the 510(k) summary for the GENORAY Fluoroscopic X-Ray System (Model: ZEN-2090 Pro). It includes information about the device, its indications for use, and a comparison to predicate devices, asserting that it is "as safe and effective as the predicate devices" based on "bench and clinical evaluation." However, it does not contain the detailed information necessary to answer your specific questions regarding acceptance criteria and a study proving those criteria are met.

    This document is a regulatory filing, and while it states the device's safety and effectiveness, it doesn't present the detailed study methodology, results, or specific acceptance criteria in the format you've requested.

    Therefore, I cannot provide a table of acceptance criteria and reported device performance, nor details about sample sizes, ground truth establishment, expert qualifications, adjudication methods, MRMC studies, or standalone performance, because this information is not present in the provided text.

    Based on the provided text, the following information is available:

    • Device Name: Fluoroscopic X-Ray System (Model: ZEN-2090 Pro)
    • Intended Use/Indications: To provide fluoroscopic and radiographic images of the patient during diagnostic, surgical and interventional procedures. Examples of clinical application may include cholangiography, endoscopy, orthopedic, neurologic, stone localization, critical care and emergency room procedures i.e. surgical interventions needing X-ray imaging and/or guidance and interventions inside and outside the operating room.
    • Safety and Effectiveness Claim: "The result of bench and clinical evaluation indicates that the new device is as safe and effective as the predicate devices."
    • Predicate Devices:

    To answer your questions accurately, a different type of document, such as a detailed clinical study report or a more comprehensive performance testing report, would be required.

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