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510(k) Data Aggregation

    K Number
    K231259
    Device Name
    iRoot SP Plus
    Date Cleared
    2023-05-31

    (30 days)

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

    iRoot SP Plus

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    • Permanent obturation of the root canal following vital pulp-extirpation
    • Permanent obturation of the root canal following removal of infected or necrotic pulp and placement of intracanal dressings.
    Device Description

    iRoot SP Plus Root Canal Sealer (iRoot SP Plus) is a convenient premixed ready-to-use injectable white hydraulic cement paste developed for permanent root canal filling and sealing applications. iRoot SP Plus is an insoluble, radiopaque and aluminum-free material based on a calcium silicate composition, which requires the presence of water to set and harden. iRoot SP Plus demonstrates substantially equivalent physical properties to iRoot SP. iRoot SP Plus is packaged in a pre-loaded syringe and is supplied with disposable Tips.

    AI/ML Overview

    The provided text is a 510(k) summary for a dental device (iRoot SP Plus), specifically a root canal filling resin. It addresses the substantial equivalence to a predicate device based on non-clinical tests and the predicate device's clinical history.

    However, the document does not contain information about acceptance criteria or a study proving that an AI/ML-based device meets acceptance criteria.

    The request asks for information related to an AI/ML device's performance, such as:

    1. A table of acceptance criteria and reported device performance (for an AI/ML device)
    2. Sample sizes and data provenance for an AI/ML test set
    3. Number and qualifications of experts for AI/ML ground truth
    4. Adjudication method for AI/ML test set
    5. MRMC study details and effect size for AI assistance
    6. Standalone performance of an AI algorithm
    7. Type of ground truth used for an AI/ML device
    8. Sample size for AI/ML training set
    9. How ground truth for AI/ML training set was established

    Since the provided text is for a root canal filling resin and not an AI/ML device, none of the requested information regarding AI/ML device performance and testing is present. The document focuses on chemical composition, physical properties, and equivalence to existing root canal sealers.

    Therefore, I cannot provide the requested details based on the given input.

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    K Number
    K080917
    Device Name
    IROOT SP
    Date Cleared
    2008-04-09

    (8 days)

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

    IROOT SP

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    • Permanent obturation of the root canal following vital pulp-extirpation.
    • Permanent obturation of the root canal following removal of infected or necrotic pulp and placement of intracanal dressings.
      iRoot SP is suitable for use in the single cone and lateral condensation technique.
    Device Description

    iRoot SP Root Canal Sealer (iRoot SP) is a convenient premixed ready-to-use injectable white hydraulic cement paste developed for permanent root canal filling and sealing applications. iRoot SP is an insoluble, radiopaque and aluminum-free material based on a calcium silicate composition, which requires the presence of water to set and harden. iRoot SP does not shrink during setting and demonstrates excellent physical properties. iRoot SP is packaged in a pre-loaded syringe and is supplied with disposable Intra Canal Tips.

    AI/ML Overview

    The provided text describes the iRoot SP Root Canal Sealer and its substantial equivalence to predicate devices, but it does not contain information about acceptance criteria for device performance or the study that proves these criteria are met in the way typically associated with AI/ML medical devices (e.g., diagnostic accuracy metrics).

    Instead, this document focuses on demonstrating substantial equivalence through a comparison of physical, chemical, and biocompatible properties with established predicate devices. The "studies" mentioned are non-clinical bench and biocompatibility tests.

    Therefore, many of the requested sections (sample size, expert ground truth, adjudication, MRMC studies, standalone performance, training set details) are not applicable or cannot be extracted from this type of regulatory submission for a traditional medical device like a root canal sealer.

    Here's a breakdown of what can be extracted and what cannot:

    1. Table of Acceptance Criteria and Reported Device Performance

    The acceptance criteria are implicitly defined by the physical-chemical properties of the predicate devices. The "reported device performance" refers to the results of the non-clinical tests demonstrating that iRoot SP's properties are comparable to these predicates.

    Acceptance Criteria (Implicit from Predicates)iRoot SP Performance (demonstrated by non-clinical tests)
    Comparable FlowTested and found comparable
    Comparable Working TimeTested and found comparable
    Comparable Setting TimeTested and found comparable
    Comparable Dimensional Change following settingTested and found comparable
    Comparable SolubilityTested and found comparable
    Comparable RadiopacityTested and found comparable
    Comparable Film ThicknessTested and found comparable
    Non-mutagenicConfirmed non-mutagenic
    Non-cytotoxicConfirmed non-cytotoxic
    No allergenic potential after multiple usesBioAggregate data provides evidence; good tolerance by subcutaneous tissue

    2. Sample size used for the test set and the data provenance

    • Sample Size for Test Set: Not applicable in the context of human data or AI model output. The "test set" here would refer to the samples used in bench and biocompatibility testing, but specific numbers are not provided.
    • Data Provenance: The tests are non-clinical (bench and biocompatibility). The chemical composition is based on BioAggregate, and its biocompatibility data is referenced. This implies laboratory testing on materials, not patient data from specific countries.

    3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts

    • This is not applicable as the "ground truth" for a root canal sealer is its physical, chemical, and biocompatible properties, not a diagnostic interpretation by human experts.

    4. Adjudication method for the test set

    • Not applicable as there is no human interpretation or diagnostic labeling process.

    5. If a multi-reader multi-case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance

    • Not applicable. iRoot SP is a physical material (root canal sealer), not an AI/ML diagnostic or assistive device.

    6. If a standalone (i.e. algorithm only without human-in-the loop performance) was done

    • Not applicable. iRoot SP is a physical material, not an algorithm.

    7. The type of ground truth used

    • The "ground truth" in this context is the established physical, chemical, and biocompatibility profiles of legally marketed predicate devices (AH® Plus™ Root Canal Sealer, BioAggregate, Apexit® Root Canal Sealer, Exactech Resorbable Bone Paste, MBCP Gel™, Diapex®). The performance of iRoot SP was compared to these established profiles.

    8. The sample size for the training set

    • Not applicable as this is not an AI/ML device requiring a training set of data.

    9. How the ground truth for the training set was established

    • Not applicable as this is not an AI/ML device.
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