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510(k) Data Aggregation

    K Number
    K954394
    Manufacturer
    Date Cleared
    1996-03-07

    (171 days)

    Product Code
    Regulation Number
    882.1480
    Reference & Predicate Devices
    N/A
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Aesculap's ventriculoscope and associated instruments are designed for visual orientation and therapeutic neurosurgical procedures within the ventricular system, such as vetriculostomies, biopsies and removal of cysts, tumors and other obstructions.

    Device Description

    The Ventriculoscope System presented in this submission consists of eleven devices: a working channel, rigid endoscopes, flexible instruments and electrodes. The primary material of construction is stainless steel. The electrodes are coated with a biocompatible fluoropolymer.

    AI/ML Overview

    This document is a 510(k) summary for a medical device (Aesculap Ventriculoscope System) from 1995. It describes the device's intended use, technological characteristics, and sterilization methods, and claims substantial equivalence to other existing devices.

    However, the provided text does not contain any information about acceptance criteria, a study proving the device meets those criteria, or any of the detailed aspects related to performance evaluation (like sample sizes, ground truth establishment, expert qualifications, MRMC studies, or standalone performance) that your request outlines.

    Therefore, I cannot populate the requested table or answer the specific questions based on the provided input. The document focuses on regulatory submission aspects rather than detailed performance study results.

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