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510(k) Data Aggregation

    K Number
    K022675
    Date Cleared
    2002-11-07

    (87 days)

    Product Code
    Regulation Number
    872.3690
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    PRIME-DENT AUTOMIX DUAL CURE CORE BUILD UP MATERIAL

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

    Prime-Dent® Automix Dual Cure Core Build Up Material principal use is a dental core build-up material either with adhesives or with pins or posts.

    Device Description

    Prime-Dent® Automix Dual Cure Core Build-Up Material

    AI/ML Overview

    This is an FDA Premarket Notification (510(k)) K022675 for a dental material (Prime-Dent® Automix Dual Cure Core Build-Up Material), not a medical device that would typically undergo studies to demonstrate performance against computational acceptance criteria. The document is primarily concerned with establishing substantial equivalence to a predicate device based on material properties and intended use.

    Therefore, the requested information regarding acceptance criteria, study details, sample sizes, expert involvement, adjudication methods, MRMC studies, standalone performance, and ground truth types is not applicable to this type of submission.

    The FDA's review for this device focused on its intended use as a "dental core build-up material either with adhesives or with pins or posts" and its classification as a "Tooth Shade Resin Material" under 21 CFR 872.3690. Substantial equivalence was determined based on comparisons to legally marketed predicate devices, not through a performance study against specific computational metrics.

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