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510(k) Data Aggregation

    K Number
    K130421
    Manufacturer
    Date Cleared
    2013-08-14

    (175 days)

    Product Code
    Regulation Number
    872.3275
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    • Luting of metal-based crowns, bridges, inlays and onlays
    • Luting of high-strength all-ceramic crowns and bridges (such as aluminum oxide, lithium di silicate and zirconium oxide ceramics)
    • Luting of metal-based and high-strength all-ceramic crowns and bridges (such as aluminum oxide, lithium disilicate and zirconium oxide ceramics) on implant abutments
    • Luting of metal root posts or indirect metal post core build-ups
    • Luting of prefabricated steel crowns
    • Luting of orthodontic bands
    Device Description

    Not Found

    AI/ML Overview

    I am sorry, but the provided text is a 510(k) premarket notification and does not contain the information requested to describe the acceptance criteria and the study that proves the device meets those criteria. The document is an FDA letter confirming the substantial equivalence of MOCO GmbH's Meron Application Capsules to a legally marketed predicate device, along with the device's indications for use.

    It does not include details on:

    1. A table of acceptance criteria and reported device performance.
    2. Sample sizes for test sets or data provenance.
    3. Number and qualifications of experts for ground truth.
    4. Adjudication methods.
    5. Multi-reader multi-case (MRMC) comparative effectiveness studies.
    6. Standalone algorithm performance.
    7. Type of ground truth used.
    8. Sample size for the training set.
    9. How ground truth for the training set was established.
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