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510(k) Data Aggregation

    K Number
    K092534
    Manufacturer
    Date Cleared
    2009-12-07

    (110 days)

    Product Code
    Regulation Number
    892.5700
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    ALATUS VAGINAL BALLOON PACKING SYSTEM

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

    The ALATUS Vaginal Balloon Packing System is a single use, non-sterile, disposable, flexible, inflatable, non-powered positioning device, intended to be used on a daily treatment basis for the temporary positioning of the vaginal wall and adjacent structural anatomies. The purpose of the device is to displace and stabilize the vaginal wall during computed tomography (CT) exam, x-ray, or radiation treatment (RT) therapy. The placement of the balloon requires a physician or physician directed healthcare professional, and it is performed as a separate procedure outside of the standard (CT) exam and (RT) treatment. This device is not intended to be inserted into the uterine cavity.

    Device Description

    The ALATUS Vaginal Balloon Packing System is designed as an immobilizer to assist in positioning and displacing the vaginal wall in a more predictable and reproducible location during computed tomography (CT) exams and radiation treatment (RT) therapy. The proposed device is a latex free balloon made from Polyurethane consisting of the following components:

    1. Balloon
    2. Catheter tubing
    3. Connector
    4. Flex tubing
    5. 1-way stopcock, 90° turn handle
    AI/ML Overview

    The provided text is a 510(k) summary for the ALATUS Vaginal Balloon Packing System. It focuses on demonstrating substantial equivalence to predicate devices and does not contain information about acceptance criteria, specific performance studies with sample sizes, expert qualifications, or ground truth establishment relevant for an AI/ML medical device.

    Therefore, I cannot fulfill your request for the tables and sections regarding acceptance criteria and performance study details. The document primarily addresses regulatory clearance based on substantial equivalence, rather than a detailed performance study as would be expected for an AI/ML device.

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