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510(k) Data Aggregation

    K Number
    K062951
    Date Cleared
    2006-12-12

    (74 days)

    Product Code
    Regulation Number
    872.5570
    Panel
    Dental
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K962516, K972061, K060388

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

    To reduce or alleviate night time snoring and mild to moderate obstructive sleep apnea (OSA).

    Device Description

    The TAP III Anti-Snoring device is comprised of:

    • Lower tray fitted over the lower teeth.
    • Upper tray fitted over the upper teeth.
    • Impression material
    • Hook and Base mechanism to attach lower tray to upper tray.
    AI/ML Overview

    The provided text is a summary of safety and effectiveness for a medical device (TAP III), not a study. It compares the TAP III to predicate devices but does not describe acceptance criteria for studies or report device performance against such criteria in the way a clinical study would. The document states "Non applicable under Section 514" for "Performance Testing," indicating that a new performance study was not required for this 510(k) submission.

    Therefore, the following information cannot be extracted from the provided text:

    • Acceptance criteria and reported device performance (as these relate to a study's outcomes)
    • Sample size used for the test set and data provenance
    • Number of experts used to establish ground truth and their qualifications
    • Adjudication method
    • Multi-reader multi-case (MRMC) comparative effectiveness study details
    • Standalone performance details
    • Type of ground truth used
    • Sample size for the training set
    • How ground truth for the training set was established

    The only performance-related information mentioned is a "Reduced AHI in patients" of "72%" for the TAP III, which is also listed for all predicate devices. This appears to be a characteristic of the device type rather than a specific result from a study conducted on the TAP III itself for this submission. The document explicitly states "Non applicable under Section 514" for Performance Testing, suggesting that the substantial equivalence of the TAP III to existing devices means a new performance study was not deemed necessary by the FDA for this particular submission.

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    K Number
    K061732
    Device Name
    TAP-T
    Date Cleared
    2006-07-12

    (22 days)

    Product Code
    Regulation Number
    872.5570
    Panel
    Dental
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K962516, K972061, K060388

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

    To reduce or alleviate night time snoring and mild to moderate obstructive sleep apnea (OSA).

    Device Description

    The TAP T Anti -- snoring device is comprised of -- - 트 Lower tray fitted over the lower teeth. - . Upper tray fitted over the upper teeth. - 트 Impression material - . Hook mechanism to attach to lower tray to upper tray

    AI/ML Overview

    I am sorry, but based on the provided text, there is no information about acceptance criteria or a study that proves the device meets any specific criteria. The document is a 510(k) premarket notification summary for the TAP T device, outlining its description, intended use, and substantial equivalence to predicate devices, but it does not contain details of any performance studies or acceptance criteria.

    Therefore, I cannot provide the requested information.

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