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510(k) Data Aggregation

    K Number
    K051797
    Device Name
    FUTURE WASH/YPS
    Date Cleared
    2005-07-21

    (16 days)

    Product Code
    Regulation Number
    872.3660
    Panel
    Dental
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    FUTURE WASH/YPS

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

    Future Wash (Future Wash Light Body, Future Wash Light Body Quick Step, Future Wash Regular Body, Future Wash Regular Body Quick Step): Wash material for all kinds of dual phase impression techniques.

    YPS (YPS Penta™ HB Quick Step): Tray material for all kinds of dual phase impression techniques.

    Device Description

    Future Wash and YPS are classified as Impression materials (21 C.F.R. § 872.3660) because they are devices intended to reproduce the structure of a patient's teeth.

    Future Wash will be available as wash material in two different viscosities (light body, regular body), each of them in a regular-sct and a quick-set version, and YPS will be a tray material in a quick-set version.

    The Future Wash materials are two component (base paste/catalyst) materials designed to be used in 3M ESPE's mixing, dosing and dispensing device, Garant™. YPS is a two component (base paste/catalyst) materials to automatically be mixed and dispensed in the 3M ESPE's Pentamix™ 2 device.

    AI/ML Overview

    The provided text is a 510(k) summary for dental impression materials (Future Wash and YPS Penta™), not a study demonstrating a device meets acceptance criteria. It discusses the substantial equivalence of the new devices to predicate devices. Therefore, I cannot extract the specific information requested about acceptance criteria and a study proving device performance as such a study is not detailed in the provided text.

    The information provided confirms:

    • The devices are dental impression materials.
    • The submission is a special 510(k) for modifications to existing silicone impression materials.
    • Biocompatibility testing was carried out to provide evidence for safety.
    • Performance characteristics were compared to predicate devices to prove effectiveness.
    • The conclusion is that the new devices are substantially equivalent to their predicate devices.

    However, the summary does not include:

    1. A table of acceptance criteria and reported device performance.
    2. Sample sizes for a test set, data provenance, or details on retrospective/prospective studies.
    3. The number or qualifications of experts used for ground truth.
    4. Adjudication methods.
    5. Details of a multi-reader multi-case (MRMC) comparative effectiveness study, effect sizes, or human reader improvement with/without AI assistance.
    6. Details of a standalone algorithm-only performance study.
    7. The type of ground truth used (e.g., expert consensus, pathology, outcomes data).
    8. Sample size for the training set.
    9. How ground truth for the training set was established.

    Therefore, I cannot fulfill the request based on the provided text.

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