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510(k) Data Aggregation

    K Number
    K981383
    Device Name
    ALLOYBOND
    Date Cleared
    1998-06-16

    (61 days)

    Product Code
    Regulation Number
    872.3200
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Dentin and Enamel adhesive for use with amalgam and resin based restorative materials.

    Device Description

    Not Found

    AI/ML Overview

    This an FDA approval letter for a device named Alloybond, which is a Dentin and Enamel adhesive. The letter mentions that the device is "substantially equivalent" to devices marketed before May 28, 1976. However, the provided document does not contain any information regarding acceptance criteria, device performance details, study design (sample sizes, data provenance, expert ground truth, adjudication methods, MRMC studies), or ground truth establishment for either test or training sets. This letter confirms approval and mentions that the device can be marketed.

    Therefore, I cannot fulfill the request as the necessary information is not present in the provided text.

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