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510(k) Data Aggregation

    K Number
    K972292
    Device Name
    SOLIDEX
    Manufacturer
    Date Cleared
    1997-10-29

    (132 days)

    Product Code
    Regulation Number
    872.3690
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Solidex is a light cured, hard crown and bridge composite. It is suitable for use in the construction of crowns and bridges, telescopic and cone crowns, attachment work, implant restoration, facings, jacket crowns, inlays and onlays, long-term provisionals, and veneers. It is universal product suitable for all classes of reconstructions, provided it is supported by adequated by working framework.

    Device Description

    Solidex is a light cured, hard crown and bridge composite.

    AI/ML Overview

    The provided document is a 510(k) premarket notification letter from the FDA for a dental material called "Solidex." This document does not describe a study or acceptance criteria for a medical device that utilizes AI or other algorithmic performance metrics.

    Instead, it's a regulatory clearance for a traditional dental cement. Therefore, I cannot extract the information requested as it is not present in the provided text.

    The questions in your prompt (acceptance criteria, sample sizes, ground truth, expert qualifications, adjudication methods, MRMC studies, standalone performance, training sets) are specific to the evaluation of AI/ML-based medical devices or diagnostic tools. "Solidex" is a material, not a diagnostic or AI-driven device, so these types of evaluations are not applicable or described in this document.

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