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510(k) Data Aggregation

    K Number
    K160716
    Date Cleared
    2016-04-14

    (30 days)

    Product Code
    Regulation Number
    870.1340
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    The Nanostim Introducer Kit

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

    The Nanostim™ Introducer Kit is intended to provide a conduit into the venous system for insertion of diagnostic and other interventional devices.

    Device Description

    The St Jude Medical Nanostim Introducer Kit is designed to perform as a quiding sheath for introduction of diagnostic and interventional devices. The Nanostim™ Introducer Kit is comprised of an introducer sheath and a dilator. The Introducer Kit is compatible with 0.035" and 0.038" guidewires and is available in 18F and one length of 30 cm.

    The introducer is fitted with a hemostasis valve to minimize air introduction during insertion and/or exchange, and a sideport with a three-way stopcock. The introducer features a radiopaque tip marker incorporated within the sheath material to identify the location of the distal tip of the sheath. Design modifications were made to the current design to improve the manufacturability and to increase the product shelf life. The changes made to the Nanostim Introducer Kit do not affect the intended use of the device or alter the fundamental scientific technology of the device.

    AI/ML Overview

    The provided text is a 510(k) summary for the Nanostim Introducer Kit, which is a medical device. This document focuses on demonstrating substantial equivalence to a predicate device, rather than proving a device meets specific clinical performance criteria for accuracy or diagnostic efficacy in the way an AI or diagnostic imaging device would.

    Therefore, many of the requested categories for AI/diagnostic studies (e.g., sample size of test set, ground truth experts, MRMC studies, standalone performance) are not applicable here. This document primarily describes engineering verification and biocompatibility testing.

    Here's the information extracted from the document that is relevant to acceptance criteria and device performance:

    1. Table of Acceptance Criteria and Reported Device Performance

    Test PerformedAcceptance CriteriaReported Device Performance
    Visual testNot explicitly stated (implied to meet visual standards)All pre-determined acceptance criteria were met.
    Dimensional measurement testNot explicitly stated (implied to meet specifications)All pre-determined acceptance criteria were met.
    Tensile StrengthNot explicitly stated (implied to meet specifications)All pre-determined acceptance criteria were met.
    Torsional StrengthNot explicitly stated (implied to meet specifications)All pre-determined acceptance criteria were met.
    Liquid LeakNot explicitly stated (implied to prevent leaks)All pre-determined acceptance criteria were met.
    Simulated UseNot explicitly stated (implied to function as intended)All pre-determined acceptance criteria were met.
    Biocompatibility: CytotoxicityIn accordance with ISO 10993-1:2009 for an external communicating device with limited exposure (
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