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510(k) Data Aggregation

    K Number
    K080864
    Manufacturer
    Date Cleared
    2008-07-21

    (115 days)

    Product Code
    Regulation Number
    872.3630
    Panel
    Dental
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    CAM STRUCTSURE PRECISION MILLED BARS

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

    The CAM StructSURE® Precision Milled Bars are intended for use as an accessory to an endosseous dental implant to support a prosthetic device in a partially or edentulous patient. It is intended for use to support multiple tooth prostheses in the mandible or maxilla. The prostheses can be screw retained.

    Device Description

    All CAM StructSURE® Precision Milled Bars (Dolder, Primary, Hader, Hybrid and Copy Milled) are designed to match an individual patient. The bars are designed from a three-dimensional optical and/or digital scanner system that scans the casting of a patient's impression and then is machined using a CADCAM software system. The bars are milled from titanium alloy or CP titanium.

    CAM StructSURE® Precision Milled Bars:
    CSHxx CAM StructSURE Hader Bar: 2-10 implants
    CSPxx CAM StructSURE Primary Bar: 2-10 implants
    CSDxx CAM StructSURE Dolder Bar: 2-10 implants
    CSCMxx CAM StructSURE Copy Milled Bar: 4-10 implants
    CSIYxx CAM StructSURE Hybrid Bar: 4-10 implants

    AI/ML Overview

    The provided document is a 510(k) summary for a dental device (CAM StructSURE® Precision Milled Bars). It focuses on demonstrating substantial equivalence to a predicate device rather than presenting a performance study with detailed acceptance criteria and results as typically found for complex AI/diagnostic devices.

    Therefore, much of the requested information regarding acceptance criteria, study design elements (sample size, ground truth, experts, adjudication, MRMC, standalone), and training set details are not applicable or available within this specific document. This document is a regulatory submission for a medical device approval that is not based on a statistical study with specific performance outcomes.

    Here's an analysis based on the provided text, highlighting where information is not present:


    1. Table of Acceptance Criteria and Reported Device Performance

    Not applicable in this context. This 510(k) submission for the CAM StructSURE® Precision Milled Bars focuses on demonstrating "substantial equivalence" to a legally marketed predicate device (K034035 3i Patient Specific Overdenture Bars) rather than meeting specific quantifiable performance metrics through a clinical trial or performance study with acceptance criteria.

    The "conclusion" states: "Appropriate verification and validation activities were performed to provide assurance that CAM StructSURE® Precision Milled Bars remain substantially equivalent to the predicate and the modifications have not changed the intended use, altered the fundamental scientific technology or the safety and effectiveness of the device." This indicates general design control and validation rather than a study against a specific performance benchmark.


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

    Not applicable. The document does not describe a "test set" in the context of a statistical study for device performance. It refers to "verification and validation activities" but provides no details on sample size, data origin, or retrospective/prospective nature.


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

    Not applicable. No "ground truth" or expert review process is described for performance evaluation of this device as it is not a diagnostic or AI-driven device.


    4. Adjudication method for the test set

    Not applicable. No "test set" or adjudication method is described.


    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 device is not an AI-assisted diagnostic tool, and therefore, an MRMC study is not relevant.


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

    Not applicable. This device is a physical dental overdenture bar, not an algorithm.


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

    Not applicable. The concept of "ground truth" as it applies to performance studies for AI/diagnostic devices is not relevant here. The substantial equivalence is based on comparison to a predicate device and adherence to design controls.


    8. The sample size for the training set

    Not applicable. This device is not an algorithm that requires a "training set."


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

    Not applicable. Since there is no training set mentioned, the establishment of ground truth for it is also not applicable.

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