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510(k) Data Aggregation

    K Number
    K043284
    Device Name
    ENDOASSIST
    Date Cleared
    2005-02-25

    (91 days)

    Product Code
    Regulation Number
    876.1500
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    ENDOASSIST

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

    EndoAssist is indicated for use in general thoracoscopy, general cardiothoracic surgery, general laparoscopy, nasopharyngoscopy, ear endoscopy and sinuscopy, where a rigid laparoscope/endoscope is intended for use.

    A few examples of the more common endoscopic surgeries are laparoscopic*

    cholecystectomy hernia repair fundoplication splenectomy appendectomy hemicolectomy sympathectomy lymph node dissection hysterectomy gastric banding qastric by pass nephrectomy radical prostatectomy anterior spinal fusion, decompression fixation wedge resection lung biopsy pleural biopsy , internal mammary artery dissection for coronary artery bypass coronary artery bypass grafting where endoscopic visualization is indicated examination of the evacuated cardiac chamber during performance of valve replacement or repair.

    • In this context "laparoscopic" is taken to embrace the use of a rigid endoscope in any part of the body
    Device Description

    EndoAssist is a head-controlled Endoscopic camera manipulator. It is intended for use in minimally invasive laparoscopic, thoracoscopic, urological, gynecological and cardiac surgery and allows the surgeon directly to control movements of a rigid endoscope by head gestures.

    AI/ML Overview

    I'm sorry, but without a dedicated study section detailing performance data, acceptance criteria, and ground truth establishment, I cannot fulfill your request for a table of acceptance criteria, device performance, and study information. The provided document is a 510(k) summary for the EndoAssist device, which primarily focuses on device description, intended use, and substantial equivalence to predicate devices, rather than detailed performance study results against specific acceptance criteria.

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    K Number
    K973249
    Device Name
    ENDOASSIST
    Date Cleared
    1997-11-26

    (89 days)

    Product Code
    Regulation Number
    876.1500
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    ENDOASSIST

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

    Endo Assist positions a Laparescope, and is indicated for use laparoxopic, thoracoscopic and pelvic procedures. Laparoscopic: cholecystectory hernia repair Fundaplication Splenectomy appendectiony henicolectory synpathe ctony by oph node dissection hysterectory nysterectomy

    Device Description

    EndoAssist is a microprocessor-driven robotic arm which holds a rigid laparoscope for the surgeon during laparoscopic surgical procedures. It stands separately from the operating table, and reaches up and over into the surgical field through a series of motorized mechanical linkages. These motors allow the microprocessor to change the configuration of the linkage.

    AI/ML Overview

    The provided text does not contain information about acceptance criteria or a study proving the device meets said criteria.

    It is a 510(k) summary for the EndoAssist device, which is a robotic arm for manipulating a laparoscope during surgery. The document focuses on:

    • Device identification: Proprietary name (EndoAssist), common name, classification name.
    • Substantial equivalence claim: Comparison to predicate devices (AESOP and Endex Endoscopy Positioning System).
    • Device description: How it works, its components, and its unique technological characteristics compared to predicates.
    • Intended use: Mechanical laparoscope holder and manipulator for laparoscopic and thoracoscopic surgery.
    • Safety issues: Design features to ensure operational, electrical, and mechanical safety.
    • FDA correspondence: The FDA's letter confirming substantial equivalence and allowing the device to be marketed.
    • Indications for Use: A list of specific laparoscopic, thoracoscopic, and pelvic procedures for which the device is indicated.

    While safety features are mentioned, there is no mention of specific acceptance criteria (e.g., performance metrics, thresholds) or a study that evaluates and reports on these criteria. The determination of substantial equivalence is explicitly stated as "not based on an assessment of clinical performance data."

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