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510(k) Data Aggregation

    K Number
    K981898
    Device Name
    ORTHOVU-1000
    Manufacturer
    Date Cleared
    1998-08-03

    (63 days)

    Product Code
    Regulation Number
    892.1000
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The OrthoVu-1000 is intended to produce MRI images of human extremities, which when reviewed by a qualified medical practitioner, can render medical information of the region under review.

    Device Description

    The OrthoVu-1000 is a transportable, permanent-magnet MRI system, which uses a surface magnet/coil assembly to perform nuclear magnetic resonance imaging of human anatomy with particular emphasis on the imaging of extremities. This system utilizes a non-homogeneous magnetic field, developed by a single device head, which applies magnetic and radio frequency (RF) energy and then detects the resultant spin echoes. A computer system controls excitation and performs processing and imaging functions. The control and imaging computer as well as the associated electronics package is mounted on a cart with a magnet assembly which can be manually positioned in the correct orientation to perform the desired imaging.

    AI/ML Overview

    The provided document is a 510(k) Premarket Notification for the OrthoVu-1000 Magnetic Resonance Imaging System. It describes the device, its intended use, and its technological comparison to predicate devices. However, it does not include information about acceptance criteria, a study proving the device meets those criteria, or details regarding algorithm performance, sample sizes, expert involvement, or ground truth establishment for AI/algorithm-based testing.

    The document is purely a regulatory submission for a traditional MRI device, not an AI-powered diagnostic tool. Therefore, none of the requested information regarding acceptance criteria and study details for an AI/algorithm-based device can be extracted from this text.

    The document does not provide the information requested in the prompt as it pertains to an MRI system, not an AI-powered device.

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