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510(k) Data Aggregation

    K Number
    K103379
    Date Cleared
    2011-02-14

    (89 days)

    Product Code
    Regulation Number
    872.3770
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    TELIO CS INLAY & TELIO CS ONLAY

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

    Telio CS Inlay:
    Temporization of deep inlay preparations with paralle! walls
    Sealing of implant screw access holes
    Relining of pre-fabricated, temporary crowns and bridges made of polycarbonate or methacrylates.

    Telio CS Onlay:
    Temporization of large, shallow cavities (onlay preparations).

    Device Description

    Not Found

    AI/ML Overview

    The provided text is a letter from the FDA regarding the 510(k) premarket notification for "Telio® CS Inlay and Telio® CS Onlay." This document is a regulatory clearance letter for a dental material (temporary crown and bridge resin), not a study report or clinical trial demonstrating the performance of a medical device against acceptance criteria with AI assistance.

    Therefore, the requested information about acceptance criteria, device performance, sample sizes, expert qualifications, adjudication methods, MRMC studies, standalone performance, ground truth establishment, training set details, and AI-assisted improvements cannot be extracted from this document as it pertains to a different type of medical product and regulatory pathway.

    This document confirms substantial equivalence of a temporary dental material to a predicate device, based on its indications for use and material properties, not on a machine learning model's performance.

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