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510(k) Data Aggregation

    K Number
    K101540
    Date Cleared
    2010-10-29

    (148 days)

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

    GRANITEC DUAL-CURE CORE BUILD-UP, N'DURANCE DIMER CORE

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

    Granitec® Dual-Cure Core Build-Up is indicated for direct build-up of the crowns of teeth that have been badly broken down and are in need of a prosthetic crown in order to regain function. It is especially indicated for use under esthetic full porcelain and composite crowns, onlays and inlays where the underlying tooth structure and core restoration will show through the esthetic veneer. It can be used on vital or de-vital, endodontically treated teeth. It may be used with pins and posts and should be bonded to the tooth with a bonding agent.

    N'Durance Dimer Core is indicated for direct build-up of the crowns of teeth that have been badly broken down and are in need of a prosthetic crown in order to regain function. It is especially indicated for use under esthetic full porcelain and composite crowns, onlays and inlays where the underlying tooth structure an d core restoration will show through the esthetic veneer. It can be used on vital or de-vital, endodontically treated teeth. It may be used with pins and posts and should be bonded to the tooth with a bonding agent.

    Device Description

    Not Found

    AI/ML Overview

    This document is largely a 510(k) clearance letter from the FDA for two dental devices, Granitec® Dual-Cure Core Build-Up and N'Durance Dimer Core. It states that the devices are substantially equivalent to legally marketed predicate devices.

    The letter itself does not contain information about acceptance criteria or a study that proves the device meets specific acceptance criteria. It is a regulatory approval document based on a finding of substantial equivalence, not a detailed report of performance testing.

    Therefore, I cannot provide the requested information from the provided text. The document outlines the FDA's decision based on a review of the manufacturer's submission, but the details of the performance study and acceptance criteria are not included in this letter.

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