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510(k) Data Aggregation

    K Number
    K071429
    Manufacturer
    Date Cleared
    2007-09-10

    (110 days)

    Product Code
    Regulation Number
    872.1745
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    TI2200 TRANSILLUMINATION CABLE

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

    The Ti2200 Transillumination Cable is a diagnostic aid used to locate decay, calculus, fracture lines, endodontic orifices, cracks and fissures underneath the tooth surface utilizing a fiber optic cable and handle attached to a light source.

    Device Description

    The Ti2200 Transillumination Cable is a fiber optic transilluminator connected directly to a light source. The Ti2200 Transillumination Cable uses a 2.1mm fiber-optic bundle with a 45 degree stainless steel end-tip. The end-tip, when placed on the tooth surface (and when other sources of light are minimized), creates an illuminated tooth structure to help locate decay, calculus, fracture lines, endodontic orifices, cracks and fissures. These clinical entities reduce the ability to transmit light and therefore show up as dark areas in an otherwise bright structure thus aiding in diagnosis.

    AI/ML Overview

    The provided text describes a 510(k) submission for the Ti2200 Transillumination Cable. This device is a fiber optic transilluminator intended to help locate dental issues like decay, calculus, and cracks by illuminating the tooth structure.

    The document discusses the device description, intended use, and claims substantial equivalence to a predicate device (Addent Inc., Microlux Transilluminator). The FDA's letter states that the device is substantially equivalent to legally marketed predicate devices.

    However, the provided text does not contain any information regarding acceptance criteria, performance studies, sample sizes, ground truth establishment, expert qualifications, adjudication methods, or MRMC studies. The document is a regulatory submission for premarket notification, focusing on demonstrating substantial equivalence rather than reporting a detailed clinical or performance study.

    Therefore, I cannot fulfill the request to describe the acceptance criteria and the study that proves the device meets the acceptance criteria, as this information is not present in the provided input.

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