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510(k) Data Aggregation

    K Number
    K994268
    Device Name
    ARABESK TOP
    Manufacturer
    Date Cleared
    2000-02-03

    (48 days)

    Product Code
    Regulation Number
    872.3690
    Panel
    Dental
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Arabesk® Top is a light-curing, radiopaque ceramic microhybrid composite filling material for both anterior and posterior applications, as well as for inlay techniques. Arabesk® Top is intended for use in restoring:

    • · Class I-V fillings
    • Reconstruction of traumatically affected anteriors
    • Facetting of discolored anteriors
    • · Color and/or shape corrections to improve asthetic appearance
    • · Locking or splinting of loose anteriors
    • · Extended fissure sealaing for molars and premolars
    • · Repairing veneers
    • Core build-up under crowns
    • · Especially suited for composite inlays
    Device Description

    Arabesk Top is a light-curing, radiopaque ceramic microhybrid composite filling material for both anterior and posterior applications, as well as for inlay techniques. Arabesk Top contains 77% by weight (56% by volume) inorganic fillers, microfillers (~ 0.05um), and small particle fillers (~0.71m). The methacrylate monomers consist of BIS-GMA, UDMA, and TEDMA.
    Arabesk Top is available in bulk dispensing syringes (4gm each) and in singleuse applicator-tip capsules (0.25 gm each).

    AI/ML Overview

    The provided text is a 510(k) summary for a dental composite filling material named ARABESK® TOP. It focuses on establishing substantial equivalence to existing predicate devices based on material composition and performance properties. The document does not describe a study that uses a test set, experts, ground truth, or an AI algorithm to measure device performance against acceptance criteria. Therefore, most of the requested information cannot be extracted.

    Here's an analysis based on the provided text:

    1. A table of acceptance criteria and the reported device performance

    The document does not explicitly state quantitative acceptance criteria or a direct measurement of ARABESK® TOP's performance against such criteria. Instead, it claims substantial equivalence to predicate devices (Tetric Ceram and Charisma) based on similar compositional and performance properties.

    Acceptance CriteriaReported Device Performance (ARABESK® TOP)
    Compositional Similarity:Formulated from chemical components common in marketed dental composites (BIS-GMA, UDMA, TEDMA, inorganic fillers).
    - Inorganic silicates (w/w)~72-77% (similar to predicates)
    - Methacrylates (w/w)~20-22% (similar to predicates)
    - Photoinitiators and Pigments (w/w)~1% (similar to predicates)
    Performance Properties:Substantially alike with predicate devices.
    - Compressive strengthNot explicitly quantified, but claimed to be "substantially alike" with predicates.
    - Polymerization shrinkageNot explicitly quantified, but claimed to be "substantially alike" with predicates.
    - Color stabilityNot explicitly quantified, but claimed to be "substantially alike" with predicates.
    - Resistance to abrasionNot explicitly quantified, but claimed to be "substantially alike" with predicates.
    Safety, Effectiveness, Biocompatibility:"Raises no new issues or questions" regarding these aspects compared to existing dental composite products.

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

    Not applicable. The document describes a comparison to predicate devices, not a study involving a test set of data.

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

    Not applicable. The document does not describe a study involving human experts establishing ground truth.

    4. Adjudication method (e.g. 2+1, 3+1, none) for the test set

    Not applicable. The document does not describe a study involving adjudication.

    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. This is a dental material submission, not an AI-assisted diagnostic device.

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

    Not applicable. This is a dental material submission, not an AI-driven algorithm.

    7. The type of ground truth used (expert consensus, pathology, outcomes data, etc)

    Not applicable. The "ground truth" in this context is the established safety and effectiveness profile of the predicate devices. The claim is that ARABESK® TOP performs "substantially alike" to these already regulated products.

    8. The sample size for the training set

    Not applicable. The document does not describe a training set as it is not a machine learning/AI device.

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

    Not applicable. The document does not describe a training set or its ground truth establishment.

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