Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K182780
    Device Name
    XP Composite
    Date Cleared
    2019-07-03

    (275 days)

    Product Code
    Regulation Number
    872.3690
    Panel
    Dental
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    • Restoration of deciduous teeth
    • Posterior restorations (class I and II)
    • Anterior restorations (class III and IV)
    • Class V restorations
    • Veneering of discoloured anterior teeth
    • Splinting of mobile teeth
    • Extended fissure sealing in molars and premolars
    • Repair of composite and ceramic veneers
    Device Description

    "XP Composite" is a light cure composite.

    AI/ML Overview

    The provided text is a 510(k) Summary for a dental restorative material, "XP Composite." It describes the device, its intended use, and its substantial equivalence to a predicate device, Tetric EvoCeram. This document does NOT contain information about an AI/ML-based medical device study, nor does it provide details about acceptance criteria and performance data in the context of an AI/ML algorithm.

    Therefore, I cannot fulfill your request to describe the acceptance criteria and the study that proves the device meets the acceptance criteria, including:

    1. A table of acceptance criteria and the reported device performance
    2. Sample size used for the test set and the data provenance
    3. Number of experts used to establish the ground truth for the test set and their qualifications
    4. Adjudication method for the test set
    5. If a multi-reader multi-case (MRMC) comparative effectiveness study was done and its effect size
    6. If a standalone (algorithm only) performance study was done
    7. The type of ground truth used
    8. The sample size for the training set
    9. How the ground truth for the training set was established

    The document focuses on the physical and chemical characteristics, intended use, and non-clinical performance data (e.g., compressive strength, water sorption) of a dental composite material to demonstrate substantial equivalence to a predicate device, as required for a 510(k) submission. It's a traditional medical device clearance, not an AI/ML device.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1