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510(k) Data Aggregation

    K Number
    K031341
    Device Name
    STICK FLOW
    Manufacturer
    Date Cleared
    2003-10-29

    (184 days)

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

    STICK FLOW

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

    For anterior and limited posterior restorations and sealings in dentistry
    A flowable light cure microhybrid composite for tooth filling, sealing and cementing.

    Device Description

    Stick™ Flow is a flowable composite with excellent color stability. It is flowable, aesthetic, abrasion resistant, strongly radiopaque and high gloss polish able.

    AI/ML Overview

    The provided text {0} only mentions a 510(k) summary, device description, and intended use as part of a premarket notification for a dental composite material. It then states that the device is "substantially equivalent" to a previously approved device (Aeliteflo™, K955292). The subsequent text {1, 2, 3} consists of an FDA letter approving the 510(k) notification, confirming substantial equivalence, and specifying the indications for use.

    Crucially, the provided text does not contain any information about acceptance criteria, device performance studies, sample sizes, expert ground truth establishment, adjudication methods, MRMC studies, or standalone algorithm performance, as these are typically not included in the brief type of 510(k) summary provided here.

    Therefore, I cannot fulfill the request to build the table and answer the questions based on the given input, as the necessary information is absent. The document focuses on regulatory approval based on substantial equivalence, not on detailed performance study results.

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