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510(k) Data Aggregation

    K Number
    K112078
    Manufacturer
    Date Cleared
    2012-03-19

    (242 days)

    Product Code
    Regulation Number
    872.3820
    Panel
    Dental
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    ENDOCEM MTA (MINERAL TRIOXIDE AGGREGATE)

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    • A root-end filling material
    • For the repair of root canals as an apical plug during apexification
    • For repair of root perforations during root canal therapy
    • As a consequence of internal resorption
    • As a pulp capping material
    • For the filling of pulpotomy of deciduous tooth
    Device Description

    This product is designed for vital pulp therapies like direct pulp capping treatment. It effectively prevents secondary infection as well as pulp irritation.

    AI/ML Overview

    The provided text describes a 510(k) summary for the medical device ENDOCEM MTA (Mineral Trioxide Aggregate). The submission focuses on demonstrating substantial equivalence to a predicate device rather than presenting a detailed clinical study with acceptance criteria for device performance in a clinical setting.

    Therefore, many of the requested sections below are not applicable because the submission relies on demonstrating comparable physical and biocompatible properties to a predicate device, not on proving clinical efficacy against specific acceptance criteria in a study.


    1. Table of Acceptance Criteria and Reported Device Performance

    Not applicable. The submission does not define specific "acceptance criteria" in terms of clinical performance metrics (e.g., sensitivity, specificity, accuracy) for the device. Instead, the acceptance criteria for the device evaluation were based on meeting ISO 6876 standards for physical properties and demonstrating similar physical and biocompatible properties to the predicate device.

    Acceptance Criteria (from ISO 6876)Reported Device Performance
    Setting timeMet test criteria
    SolubilityMet test criteria
    Dimensional change following settingMet test criteria
    RadiopacityMet test criteria

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

    Not applicable. This submission does not describe a clinical "test set" in the context of an effectiveness study. The evaluation focused on bench testing (physical characteristics) and biocompatibility, comparing the new device to a predicate device. Information on sample sizes for these tests (e.g., number of samples for setting time measurement) is not provided in the summary.

    The data provenance is from bench and biocompatibility testing performed by the manufacturer, MARUCHI, located in South Korea. The study is not a retrospective or prospective clinical study on human subjects.

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

    Not applicable. No clinical "test set" requiring ground truth established by experts is described in this submission. The evaluation was based on standardized physical property tests (ISO 6876) and biocompatibility assessments, not on interpretation of clinical data by experts.

    4. Adjudication Method for the Test Set

    Not applicable. As there is no clinical "test set" requiring ground truth established by experts, no adjudication method was used.

    5. If a Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study Was Done

    No. A MRMC comparative effectiveness study was not done. The submission is a 510(k) for substantial equivalence based on physical and biocompatibility properties, not a clinical efficacy study involving human readers.

    6. If a Standalone (Algorithm Only Without Human-in-the-Loop Performance) Was Done

    Not applicable. This device is a dental material (root filling material), not a software algorithm or an AI-powered system that would have "standalone performance" in the context of an algorithm's output without human intervention.

    7. The Type of Ground Truth Used

    The "ground truth" for the device evaluation was based on:

    • ISO 6876 standards: For physical properties like setting time, solubility, dimensional change, and radiopacity. The values defined by this international standard serve as the reference.
    • Predicate device properties: The submission states that the new device has "similar physical and biocompatible properties" and "comparable performance specifications" to the predicate device (MTA MATERIAL, K981620). The properties of the predicate device, demonstrated to be safe and effective, represent an implicit "ground truth" for equivalence.

    8. The Sample Size for the Training Set

    Not applicable. This submission describes a new medical device, not an AI or machine learning algorithm that requires a "training set."

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

    Not applicable. As there is no training set for an algorithm, the concept of establishing ground truth for a training set does not apply.

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