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510(k) Data Aggregation

    K Number
    K042171
    Date Cleared
    2004-11-10

    (91 days)

    Product Code
    Regulation Number
    872.4200
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Ax's Endo® handpieces are intended to hold burs or other tools and to transmit power to these via a motor.

    Device Description

    Ax's Endo® handpieces are intended to hold burs or other tools and to transmit power to these via a motor.

    AI/ML Overview

    This is an FDA 510(k) clearance letter for the Ax's Endo® dental handpiece. This document is a regulatory approval, not a scientific study report. Therefore, it does not contain information regarding acceptance criteria for a device's performance based on a study, nor does it describe a study proving the device meets particular criteria.

    The letter states that the device is "substantially equivalent" to legally marketed predicate devices, which is the basis for 510(k) clearance. This means the FDA found that the new device is as safe and effective as a legally marketed device that is not subject to PMA.

    Therefore, I cannot fulfill your request for the specific points about acceptance criteria and a study from the provided document.

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