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510(k) Data Aggregation

    K Number
    K053592
    Manufacturer
    Date Cleared
    2006-02-08

    (47 days)

    Product Code
    Regulation Number
    892.2050
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    SIMPLANT DR. JAMES

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

    The Materialise SimPlant System is intended for use as a software interface and image segmentation system for the transfer of imaging information from a medical image boginemation bytten or a Magnetic Resonance scanner. It is also used as a scannel such as a O P Sounterial implant placement and surgical treatment options.

    Device Description

    The modified SimPiant System is used to transfer images from a medical scanner and to perform a segmentation of the images. It is also used to provide a means for pre-operative planning. Surgical templates may be fabricated based on the output of the pre-operative planning.

    AI/ML Overview

    The provided text does not contain information about acceptance criteria, device performance, or any studies conducted. The document is a 510(k) premarket notification summary and an FDA clearance letter for a modified SimPlant System. It primarily discusses the device's intended use, functions, and a comparison with a predicate device to establish substantial equivalence. There is no data regarding sample sizes, expert qualifications, adjudication methods, MRMC studies, standalone performance, or details on how ground truth was established for training or testing sets.

    Therefore, I cannot provide the requested table or answer the specific questions about studies and acceptance criteria based on the given information.

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