Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K080886
    Device Name
    IPLAN RT IMAGE
    Manufacturer
    Date Cleared
    2008-06-24

    (85 days)

    Product Code
    Regulation Number
    892.5050
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    IPLAN RT IMAGE

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

    iPlan RT Image's indications for use are to prepare and present patient and image data based on CT, MR, angiographic and other imaging sources including

    • image preparation -
    • image localization
    • n image fusion
    • image segmentation "
    • isocenter handling -
    • plan review and approval -
      where the result is used for stereotactic radiation treatment planning that is intended for use in stereotactic, conformal, computer planned, LINAC based radiation treatment of cranial, head and neck and extracranial lesions.
    Device Description

    Not Found

    AI/ML Overview

    The provided text is a 510(k) summary for the iPlan RT Image device from BrainLAB AG. This document focuses on establishing substantial equivalence to predicate devices and detailing the intended use. It does not contain information about acceptance criteria, device performance studies, sample sizes, expert ground truth establishment, or any comparative effectiveness studies.

    Therefore, I cannot provide the requested information from this document. The sections you asked for, such as "A table of acceptance criteria and the reported device performance," "Sample sized used for the test set," "Number of experts used," "Adjudication method," "MRMC comparative effectiveness study," "standalone performance," "type of ground truth," "training set sample size," and "how ground truth for training set was established," are not present in the provided text.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1