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510(k) Data Aggregation

    K Number
    K190621
    Date Cleared
    2019-04-23

    (43 days)

    Product Code
    Regulation Number
    876.4300
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    SB Knife/Short type, SB Knife/Standard type, SB Knife/Jr type, SB Knife/Jr type - Long

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

    The SB Knife® is a single-use sterile Electrosurgical Knife (Model Numbers: MD-47703 W, MD-47706 and MD-47703L). This device is designed to be used with Olympus and ERBE Electrosurgical monopolar HF generators, connectors and patient grounding plates to cut tissue including Zenker's diverticulum within the digestive tract using high-frequency current.

    Device Description

    The SB Knife® is a single-use sterile Electrosurgical Knife (Model Numbers: MD-47703 W, MD-47706 and MD-47703L).

    AI/ML Overview

    I am sorry, but the provided text does not contain information about acceptance criteria, device performance, study details, or ground truth establishment for a medical device. The document is a 510(k) clearance letter from the FDA for the SB Knife®, which states that the device is substantially equivalent to legally marketed predicate devices. It outlines regulatory requirements and indications for use, but it does not include performance study data, sample sizes, expert qualifications, or details about how ground truth was established, which are necessary to answer your request.

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