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510(k) Data Aggregation

    K Number
    K023070
    Manufacturer
    Date Cleared
    2003-01-28

    (134 days)

    Product Code
    Regulation Number
    874.4250
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K954717, K954080, K955174, K994175

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

    The Sodem High Speed System includes a pneumatic motor which allows the fixation of spindles, adapters and attachments, which operate with drills, burs and cutters for drilling, cutting and sculpting hard tissue and bone for different applications and surgeries.

    The system is intended for use in Ear Nose and Throat (plastic reconstructive surgery) applications.

    Device Description

    The Sodem High Speed System is a modular pneumatically powered high speed instrument system consisting of a hand piece, adapters and accessories/attachments (spindles, burs ... ) used to cut hard tissue or bone.

    The Sodem High Speed System (Pneumatic) is a complete system including:

    • a High Speed motor, -
    • a foot pedal,
    • dedicated hoses to connect the motors and the foot pedal, -
    • adapters (angled adapter)
    • attachments/spindles, (angled attachments, straight attachments standard and tapered, craniotomes)
    • drills, burs and cutters
    AI/ML Overview

    The Sodem High Speed System (Pneumatic) is a surgical instrument motor and accessories intended for use in Ear, Nose, and Throat (plastic reconstructive surgery) applications. It is designed to drill, cut, and sculpt hard tissue and bone.

    Here's an analysis of its acceptance criteria and the study proving it meets these criteria:

    1. Table of Acceptance Criteria and Reported Device Performance

    The device's acceptance criteria are based on demonstrating substantial equivalence to predicate devices, specifically the Anspach Black Max/Micromax systems. The "reported device performance" in this context refers to the characteristics and specifications of the Sodem High Speed System Pneumatic) itself, which are compared against the predicate.

    Feature/Acceptance Criteria (Predicate)Reported Device Performance (Sodem High Speed System)
    Used in ENT surgeryYes
    Pneumatic power sourceYes
    Drill FunctionYes
    Supplied non sterile (except burs)Yes (except burs)
    Recommended sterilization by steamYes
    Patient contact materials: Principally surgical stainless steelYes (Surgical stainless steel and titanium (Ti 6-Al 4-V))
    Angled nose pieceYes
    Foot pedalYes
    Spindles multiple lengthYes
    Change burs without wrenchYes
    Change spindles without wrenchYes
    Motor speed (RPM)0-85'000 rpm
    Rotation modeForward only

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

    This submission is a 510(k) Pre-Market Notification based on substantial equivalence, not a clinical trial evaluating device performance with patient data. Therefore, there is no "test set" in the traditional sense (i.e., a set of patient cases or samples) for which data provenance or geographic origin would apply. The "test" consists of a comparison of the device's technical specifications and intended use against legally marketed predicate devices.

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

    As this is a substantial equivalence submission, no external experts were used to establish ground truth for a test set in the way one would for evaluating diagnostic accuracy or clinical outcomes. The "ground truth" is established by the detailed technical specifications and intended uses of the predicate devices already cleared by the FDA. The FDA reviewers (Office of Device Evaluation, Center for Devices and Radiological Health) act as the authoritative body in determining if the comparison demonstrates substantial equivalence.

    4. Adjudication method for the test set

    Not applicable. There was no test set requiring expert adjudication. The determination of substantial equivalence was made by the FDA's Office of Device Evaluation.

    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 a powered surgical drill, not an AI-assisted diagnostic tool or imaging system. Therefore, no MRMC study or evaluation of human reader improvement with AI assistance was performed.

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

    Not applicable. This device is a mechanical surgical instrument, not an algorithm.

    7. The type of ground truth used

    The "ground truth" is the technical specifications, intended use, and performance characteristics of the legally marketed predicate devices (Anspach Black Max/Micromax System and others). The applicant compared their device's attributes against these established products to demonstrate substantial equivalence.

    8. The sample size for the training set

    Not applicable. This is a conventional medical device, not an AI/ML-driven device that requires a training set.

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

    Not applicable. No training set was used.

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