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510(k) Data Aggregation

    K Number
    K083610
    Manufacturer
    Date Cleared
    2008-12-17

    (9 days)

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

    FILTEK SUPREME ULTRA UNIVERSAL RESTORATIVE

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    • Direct anterior and posterior restorations (including occlusal surfaces)
    • Core Build-ups
    • Splinting
    • Indirect restorations including inlays, onlays and veneers
    Device Description

    Filtek™ Supreme Ultra Universal Restorative is a visible-light activated, radiopaque, restorative composite.

    AI/ML Overview

    Here's a summary of the acceptance criteria and the study details for the 3M ESPE Filtek™ Supreme Ultra Universal Restorative, based on the provided text:

    Device: Filtek™ Supreme Ultra Universal Restorative


    1. Table of Acceptance Criteria and Reported Device Performance

    The provided text does not explicitly state numerical acceptance criteria for each physical property. Instead, it indicates that the new device's performance was compared to a predicate device (3M™ ESPETM HAUR) to establish substantial equivalence. The "reported device performance" is essentially that the new device performed comparably or acceptably against the predicate in these properties.

    Property EvaluatedAcceptance Criteria (Implied)Reported Device Performance
    Compressive strengthSubstantially equivalent to predicate device 3M™ ESPETM HAUR.Data from bench testing shows performance comparable to the predicate.
    Diametral Tensile StrengthSubstantially equivalent to predicate device 3M™ ESPETM HAUR.Data from bench testing shows performance comparable to the predicate.
    Flexural strengthSubstantially equivalent to predicate device 3M™ ESPETM HAUR.Data from bench testing shows performance comparable to the predicate.
    Flexural ModulusSubstantially equivalent to predicate device 3M™ ESPETM HAUR.Data from bench testing shows performance comparable to the predicate.
    Surface hardnessSubstantially equivalent to predicate device 3M™ ESPETM HAUR.Data from bench testing shows performance comparable to the predicate.
    Radio-opacitySubstantially equivalent to predicate device 3M™ ESPETM HAUR.Data from bench testing shows performance comparable to the predicate.
    Water SorptionSubstantially equivalent to predicate device 3M™ ESPETM HAUR.Data from bench testing shows performance comparable to the predicate.
    Water SolubilitySubstantially equivalent to predicate device 3M™ ESPETM HAUR.Data from bench testing shows performance comparable to the predicate.
    Polish RetentionSubstantially equivalent to predicate device 3M™ ESPETM HAUR.Data from bench testing shows performance comparable to the predicate.
    FluorescenceSubstantially equivalent to predicate device 3M™ ESPETM HAUR.Data from bench testing shows performance comparable to the predicate.
    BiocompatibilitySafe for intended use based on standard risk assessment techniques and FDA/international guidelines.Concluded to be safe for its intended use.

    2. Sample Size Used for the Test Set and Data Provenance

    The document states that data included "bench testing to evaluate the performance." However:

    • Sample Size: The specific sample sizes for each bench test are not mentioned in the provided text.
    • Data Provenance: The provenance is bench testing, which implies controlled laboratory conditions. There is no information regarding country of origin, nor whether it was retrospective or prospective, as these terms are generally not applicable to bench testing of material properties.

    3. Number of Experts Used to Establish the Ground Truth for the Test Set and Qualifications

    • Number of Experts: This information is not applicable as the study described is bench testing of physical properties, not a clinical study involving human interpretation or expert ground truth for medical imaging/diagnosis.
    • Qualifications of Experts: Not applicable.

    4. Adjudication Method for the Test Set

    • Adjudication Method: Not applicable for this type of bench testing. Adjudication methods like 2+1 or 3+1 are used for clinical trials where multiple experts assess cases and resolve discrepancies.

    5. Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study

    • MRMC Study: No, an MRMC comparative effectiveness study was not done. This type of study is relevant for diagnostic devices involving human interpretation (e.g., radiologists reading images with and without AI assistance). The provided study is bench testing of material properties.
    • Effect Size: Not applicable.

    6. Standalone (Algorithm Only Without Human-in-the-Loop Performance) Study

    • Standalone Study: Not applicable. This concept applies to AI algorithms operating independently to produce a diagnostic output. The described study evaluates the physical properties of a dental restorative material through bench testing.

    7. Type of Ground Truth Used

    • Type of Ground Truth: The "ground truth" for this study comes from objective measurements of the physical properties (e.g., strength, hardness, radio-opacity) of the material as determined by standardized laboratory bench tests. The performance of the new device was compared against a legally marketed predicate device, implying that the predicate's established performance served as a benchmark for "acceptable" property values.

    8. Sample Size for the Training Set

    • Sample Size: This information is not applicable. The device is a dental restorative material and its evaluation involved bench testing of its physical properties, not machine learning or AI models that require training sets.

    9. How the Ground Truth for the Training Set Was Established

    • Ground Truth Establishment: Not applicable as there is no training set for this type of device evaluation.
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