Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K213093
    Device Name
    STEP-1 PumEtch
    Manufacturer
    Date Cleared
    2022-01-28

    (126 days)

    Product Code
    Regulation Number
    872.3200
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K062166, K192273

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

    STEP-I PumEtch is a prophylaxis and phosphoric acid etchant treatment intended for the smface preparation of dentin or enamel prior to tooth restoration, including the application of sealants or for bonding.

    Device Description

    STEP-1 PumEtch is a tooth preparation formulation combining a 37% phosphoric acid etch and pumice, a polishing agent, into one gel liquid solution. The product is used to prepare natural tooth surfaces for the application of sealants or direct bond appliances.

    AI/ML Overview

    This describes the acceptance criteria and study proving the device meets them, based on the provided text:

    The document is a 510(k) summary for a dental product called STEP-1 PumEtch, which is a prophylaxis and phosphoric acid etchant. The primary method for proving substantial equivalence to predicate devices is through comparative performance testing.

    1. Table of Acceptance Criteria and Reported Device Performance

    Acceptance Criteria (Proxy)Reported Device Performance (Comparative to Predicate)
    No statistically significant difference in Shear Bond Strength (SBS)Demonstrated no statistically significant difference in SBS
    No statistically significant difference in pHDemonstrated no statistically significant difference in pH

    Note: The document implies these are the acceptance criteria by stating that the comparative performance testing "demonstrated there is no statistically significant difference between the subject and predicate devices" for these metrics.

    2. Sample Size Used for the Test Set and Data Provenance

    The document does not explicitly state the sample size used for the test set or the data provenance (e.g., country of origin, retrospective or prospective) for the Shear Bond Strength (SBS) and pH comparative performance testing.

    3. Number of Experts Used to Establish the Ground Truth for the Test Set and Qualifications

    This information is not applicable and not provided. The study focuses on direct physical and chemical property comparisons (SBS, pH) rather than expert-based ground truth.

    4. Adjudication Method for the Test Set

    This is not applicable and not provided. The study design involves direct measurement and comparison of physical/chemical properties.

    5. Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study

    No. An MRMC comparative effectiveness study was not done. The device is a dental etchant, not an AI or imaging device that would typically involve human readers.

    6. Standalone (Algorithm Only Without Human-in-the-Loop Performance) Study

    No. A standalone algorithm study was not done. The device is a physical/chemical product, not an algorithm.

    7. Type of Ground Truth Used

    The ground truth or reference for evaluation in this context is the performance of legally marketed predicate devices in terms of Shear Bond Strength and pH. The study aims to show that the new device performs equivalently to these established benchmarks.

    8. Sample Size for the Training Set

    This is not applicable and not provided. The device is a physical/chemical product, not an AI model that requires a training set.

    9. How the Ground Truth for the Training Set Was Established

    This is not applicable and not provided for the same reasons as above.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1