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510(k) Data Aggregation

    K Number
    K110090
    Manufacturer
    Date Cleared
    2011-05-26

    (134 days)

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

    K991601, P040002/S021

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

    The AFX Introducer System facilitates the introduction of guidewires, and other medical devices into the vasculature and minimizes blood loss associated with such introduction.

    Device Description

    The Endologix AFX Introducer System consists of an Introducer Sheath (45 cm working length) and two Dilators. The system is enclosed in a sterile package. During clinical use, the system will allow introduction of a standard 0.035" guidewire within its inner lumen.

    Introducer Sheath: The Introducer Sheath provides a conduit for introducing other interventional devices, including guidewires and interventional catheters, into the vasculature. The main components of this assembly are a hydrophilically-coated, PTFE lined, 55D Pebax introducer sheath, acrylobutylstyrene (ABS) hemostasis valve housing with butyl rubber valve, and silicone gasket assembly, 3 way stopcock/valve, and sideport diethylhexyl phthalate (DEHP)-free polyvinylchloride (PVC) tubing. The Pebax introducer sheath also includes an embedded stainless steel braid for increased strength and kink resistance, and embedded Vectran® strands for increased longitudinal strength. The distal tip of the introducer sheath includes an embedded radiopaque marker composed of 90% Platinum/10% Iridium.

    Dilators: The dilators for the system are used to provide support and stability to the Introducer Sheath during deployment into the vasculature. The dilators are designed specifically for the Endologix AFX Introducer System and can accommodate a 0.035" guidewire through the central lumen. Two dilators are included with the AFX Introducer System. Both dilators are included within the package. One dilator is a single lumen device and one dilator is a dual lumen device. Both dilators are composed of 63D Pebax with 20% Barium Sulfate (BaSO4) for radiopacity and include a hydrophilic coating on the outer surface. These dilators are designed in diameter and length to be placed within the AFX Introducer Sheath component. The dilators have a tapered, atraumatic distal tip. The proximal end of the dilators includes a luer port. The dilators provide stiffness to the assembly so that the introducer sheath can be placed within the vasculature during a standard vascular access.

    AI/ML Overview

    The provided document describes the Endologix AFX Introducer System, an introducer sheath and dilator system. The information outlines various tests conducted to demonstrate the device's substantial equivalence to predicate devices, focusing on regulatory and performance aspects.

    Here's a breakdown of the requested information based on the provided text:

    1. Table of Acceptance Criteria and Reported Device Performance

    The document presents several tables detailing various tests performed on the Endologix AFX Introducer System. The "Result (Pass/Fail)" column serves as the reported device performance against the implied acceptance criteria for each test.

    Test CategorySpecific Test / Acceptance Criteria DescriptionReported Device Performance (Result)
    SterilizationValidation of the ethylene oxide sterilization cycle in accordance with ISO 11135-1 to verify that the ethylene oxide sterilization process provides a SAL of 10^-6Pass
    Shelf-Life Packaging ValidationVisual inspection of the packaging to identify any anomalies that could impact integrityPass
    Bubble Emission (ASTM F2096-04) for detecting gross leaksPass
    Dye Penetration (ASTM F1929-98 (2004)) for detecting seal leaksPass
    Peel Test (ASTM F88M-09) for seal strength of flexible barrier materialsPass
    BiocompatibilityCytotoxicity (ISO 10993-5) using MEM ElutionPass
    Sensitization (ISO 10993-10) - Murine Local Lymph Node AssayPass
    Intracutaneous Reactivity (ISO 10993-10) - Intracutaneous Irritation TestPass
    Acute Systemic Toxicity (ISO 10993-11) - Acute Systemic Injection TestPass
    Hemocompatibility (ISO 10993-4): Complement Activation, Hemolysis Assay, Partial Thromboplastin Time, Platelet and Leukocyte CountsPass (for each sub-test)
    Pyrogenicity (USP ) - Rabbit Pyrogen TestPass
    Performance Testing (ISO 10555-1)Leak Testing (connection fittings and valve seal do not leak liquid when tested at 3.0 PSI)Pass
    Bond and Component Tensile Strength (break force meets or exceeds requirements)Pass
    Particle Size (USP requirements: 10-25μm 25μm
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