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510(k) Data Aggregation

    K Number
    K201703
    Date Cleared
    2021-02-24

    (247 days)

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

    Battery driven electrical drive unit with wireless foot controller to perform cleaning and polishing of tooth surfaces and fillings.

    Device Description

    The “PROXEO Twist Cordless Polishing System PL-40 H” is an electrical drive unit for cleaning and polishing tooth surfaces and fillings by use of Disposable Prophy Angles, so-called "DPAs". The system consists of - the cordless drive handpiece PL-40 H, - the wireless foot controller C-NW, - a handpiece holder, and - a charger inclusive adaptor. Its basic function is the conversion of electrical energy into a mechanical rotary motion. Power is supplied by a Li-ion battery, which is assembled in the drive handpiece and can be recharged by means of the provided charging cable. The battery is not changeable by the user. The device's application is intended in dentistry.

    AI/ML Overview

    The provided document is a 510(k) Premarket Notification for a dental device, the "PROXEO Twist Cordless Polishing System PL-40 H." This document aims to demonstrate substantial equivalence to a legally marketed predicate device, not to prove the device meets specific performance acceptance criteria for an AI/ML medical device.

    Therefore, the information required to answer your request (acceptance criteria, study details for AI/ML performance, sample sizes, expert qualifications, ground truth, etc.) is not present in the provided text. The document focuses on regulatory compliance for a traditional medical device, specifically dental handpieces, through comparison of technological characteristics and non-clinical testing for safety and electrical performance.

    The document explicitly states:

    • Clinical Testing: "Clinical performance testing was not conducted." (Page 6)
    • The comparison is based on "similarities in intended use, principles of operation, functional design and structure." (Page 6)

    In summary, the provided text does not contain the information requested about acceptance criteria and studies demonstrating performance for an AI/ML device.

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