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510(k) Data Aggregation

    K Number
    K121510
    Date Cleared
    2012-07-25

    (65 days)

    Product Code
    Regulation Number
    878.4750
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    IDRIVE ULTRA POWERED HANDLE ENDO GIA ADAPTER

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

    The iDrive ™ Ultra powered handle and En do GIA ™ adapter, when used with En do GIA ™ single use reloads have applications in abdominal, gynecological, pediatric, and thoracic surgery for resection, transection, and creation of anastomosis. It may be used for transection and resection rof liver substance, hepatic vasculature, and biliary structures and for transection and resection of pancreas.

    The iDrive ™ Ultra powered handle and Endo GIA TM adapter, when used with Endo GIA TM curved tip single use reloads, can be used to blunt dissect or separate target tissue from other certain tissue.

    The iDrive ™ Ultra powered handle and En do GIA TM adapter, when used with the Endo GIA TM Radial Reload with Tri-Staple ™ Technology, has applications in open or minimally invasive raneral abdominal, gynecologic, pediatric and thoracic surgery for resection and transection of tissue and creation of anastomosis, as well as application deep in the pelvis, i.e. low anterior resection. It may be used for transection of liver substance, hepatic vasculature and biliary structures and for transection and resection of pancreas.

    Device Description

    Surgical stapler with a powered handle, delivering implantable titanium staples.

    AI/ML Overview

    The provided submission describes a surgical stapler, the iDrive™ Ultra powered handle and Endo GIA™ adapter, and does not relate to an AI/ML device. Therefore, the requested information regarding acceptance criteria, study details, expert involvement, and ground truth for an AI/ML device is not applicable and cannot be extracted from this document.

    The document focuses on the safety and effectiveness of a physical medical device, not a software algorithm. The "Performance Data" section lists various in-vitro and in-vivo tests for the stapler's mechanical and biological properties, as well as adherence to electrical safety standards. This is typical for a traditional 510(k) submission for a non-AI device.

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