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510(k) Data Aggregation

    K Number
    K151837
    Device Name
    CS 3D Imaging
    Manufacturer
    Date Cleared
    2015-08-19

    (44 days)

    Product Code
    Regulation Number
    892.2050
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    CS 3D Imaging is digital imaging software intended to be used with Carestream's 3D extra-oral X-ray equipment by healthcare professionals to display, make measurement, print, export and store 2D and 3D views of the dento-maxillofacial and ENT (Earn, Nose and Throat) region of the human anatomy as diagnostic support.

    It is also a software application used for the management of the implant library and the virtual placement of dental implants.

    It can be used as stand-alone software in a standard computer and does not perform any radiographic image acquisition.

    Device Description

    CS 3D Imaging is digital imaging software intended to be used with Carestream's 3D extra-oral X-ray equipment by healthcare professionals to display, make measurement, print, export and store 2D and 3D views of the dento-maxillofacial and ENT (Earn, Nose and Throat) region of the human anatomy as diagnostic support.

    It is also a software application used for the management of the implant library and the virtual placement of dental implants.

    It can be used as stand-alone software in a standard computer and does not perform any radiographic image acquisition.

    AI/ML Overview

    I apologize, but the provided text from the FDA 510(k) summary for "CS 3D Imaging" is a general notification letter and an "Indications for Use" statement. It does not contain any information regarding acceptance criteria, study details, performance data, sample sizes, ground truth establishment, or expert qualifications.

    Therefore, I cannot fulfill your request to describe the acceptance criteria and the study that proves the device meets them based on the provided text.

    To answer your request, I would need a detailed performance study report or a section of the 510(k) submission specifically describing the validation studies and their results.

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