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510(k) Data Aggregation

    K Number
    K971641
    Date Cleared
    1997-07-21

    (80 days)

    Product Code
    Regulation Number
    872.3850
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    ANTIBACTERIAL GUTTA PERCHA

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

    For use in the final filling of prepared root canals in adult or decidious teeth when antibacterial activity is desired in the final filling agont. Used to promote healing effects and to help provent bacterial contamination of the canal. A root canal filler with antibacterial properties indicated in cases whore antibacterial properties coupled with excellent physical characteristics for complete filling of the root canal are needed.

    Device Description

    Antibacterial Gutta Percha

    AI/ML Overview

    This document is an FDA 510(k) clearance letter for an "Antibacterial Gutta Percha" device, K971641. The letter indicates that the device has been found substantially equivalent to predicate devices, thus allowing it to be marketed.

    However, the provided text does not contain any information regarding:

    • Acceptance criteria or reported device performance.
    • Study details (e.g., sample size, data provenance, expert qualifications, ground truth establishment, adjudication methods, MRMC studies, standalone performance, training set details).

    The letter solely focuses on the regulatory aspects of the device's clearance based on its substantial equivalence to previously marketed devices, rather than data from a clinical or performance study.

    Therefore, I cannot provide a table of acceptance criteria and reported device performance or answer the specific questions about a study, as this information is not present in the provided document.

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