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510(k) Data Aggregation

    K Number
    K030646
    Date Cleared
    2003-05-06

    (67 days)

    Product Code
    Regulation Number
    872.3310
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    BELLEGLASS POINT 4

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

    belleGlass Point 4 is a composite restoration material use with the belleGlass HP (heat and pressure) crown and bridge fabrication system to produce high wear resistance and permanent surface luster for composite crowns and bridges. belleGlass Point 4 may be used by itself or in conjunction with gold, Captek, non precious metal or a fiber re-enforced substructure.

    Device Description

    belieGlass Point 4 is a composite restoration material use with the belleGlass HP (heat and pressure) crown and bridge fabrication system to produce high wear resistance and permanent surface luster for composite crowns and bridges. belleGlass Point 4 may be used by itself or in conjunction with gold, Captek, non precious metal or a fiber re-enforced substructure. The belleGlass HP crown and bridge fabrication system is comprised of all the components necessary for a dental laboratory to fabricate composite resin-based crowns and bridges and cure them using both light activation combined with a final heat and pressure curing cycle in the belleGlass HP automatic curing device.

    AI/ML Overview

    This document is a 510(k) summary for a dental restorative material, belleGlass Point 4. It primarily focuses on demonstrating substantial equivalence to previously marketed devices and does not contain information about acceptance criteria or a study proving device performance against such criteria.

    Therefore, I cannot provide the requested information. The document does not describe:

    • A table of acceptance criteria and reported device performance.
    • Sample sizes for test sets, data provenance, number or qualifications of experts for ground truth, or adjudication methods.
    • Information about multi-reader multi-case (MRMC) comparative effectiveness studies or standalone algorithm performance.
    • The type of ground truth used, sample size for the training set, or how ground truth for the training set was established.

    This document is a regulatory submission for premarket notification, not a clinical or performance study report. Its purpose is to demonstrate that the new device is as safe and effective as a legally marketed predicate device, rather than proving its performance against specific acceptance criteria for a novel functionality.

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