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510(k) Data Aggregation

    K Number
    K053297
    Manufacturer
    Date Cleared
    2005-12-06

    (11 days)

    Product Code
    Regulation Number
    878.4400
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    ARTHROCARE 8000S COBLATOR SURGERY SYSTEM

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

    The ArthroCare 8000S Coblator Surgery System is indicated for ablation, resection, and coagulation of soft tissue and hemostasis of blood vessels in orthopedic, arthroscopic, spinal, and neurological procedures.

    Device Description

    The ArthroCare 8000S Coblator Surgery System is a bipolar, high frequency electrosurgical system consisting of three components: an electrosurgical generator called the Controller; a family of disposable, bipolar, single use Wands; and a reusable Patient Cable.

    AI/ML Overview

    The provided document is a 510(k) summary for the ArthroCare 8000S Coblator Surgery System, describing its substantial equivalence to a predicate device, the ArthroCare® System 2000 (K001588). It is not a study report that details acceptance criteria and device performance based on a specific study.

    Therefore, I cannot extract the information required to populate the table of acceptance criteria and reported device performance or other study-specific details such as sample sizes, ground truth establishment, expert information, or MRMC study results because this information is not present in the provided text.

    The document states that the new device's substantial equivalence is based on:
    "The proposed modifications in performance specifications, dimensional specifications, and labeling are not substantial changes or modifications, and do not significantly affect the safety or efficacy of the System."

    This implies that the device meets the same performance standards as the predicate device, but specific acceptance criteria and a study demonstrating this are not detailed in this 510(k) summary. Further documentation (e.g., test reports referenced in the original 510(k) submission) would be needed to answer these questions.

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