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510(k) Data Aggregation

    K Number
    K093397
    Manufacturer
    Date Cleared
    2009-12-17

    (48 days)

    Product Code
    Regulation Number
    870.1330
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Traxcess Guidewire and Traxcess Docking Wire is intended for general intravascular use, including the neuro and peripheral vasculature. The wire can be steered to facilitate the selective placement of diagnostic or therapeutic catheters. This device is not intended for use in coronary arteries.

    Device Description

    The Traxcess 14EX Guidewire consists of a 0.014" stainless steel shaft and a tapered The Traxcess 14EA Guidewire consisted organism and stainless steel coils. The distal coil minton the contains a lubricious hydrophilic coating, and the proximal shaft section is coated with PTFE and silicone.

    The Traxcess Docking Wire is an accessory used to extend the Traxcess guidewire. It The Traxess Docking Which an use assist with a nitinol pipe and is coated with PTFE and silicone.

    AI/ML Overview

    This is a 510(k) premarket notification for a medical device, the Traxcess 14EX Guidewire and Traxcess Docking Wire. The provided document focuses on demonstrating substantial equivalence to predicate devices, rather than presenting a study with specific performance metrics and acceptance criteria for a new AI/software-based device.

    Therefore, the requested information elements related to AI device performance studies, such as sample sizes for test/training sets, data provenance, ground truth establishment, expert adjudication, or MRMC comparative effectiveness studies, are not applicable to this submission.

    Here's the summary of the available information regarding acceptance criteria and device performance:

    1. Table of Acceptance Criteria and Reported Device Performance

    Bench TestingAcceptance Criteria (Implied: Pass)Reported Device Performance
    Physical attributesPassPass
    Distal tip tensile strengthPassPass
    Tip flexibilityPassPass
    Distal tip torque strengthPassPass
    Coating adherencePassPass
    TorqueabilityPassPass
    Attachment with docking wirePassPass
    Docking wire tensile strengthPassPass

    Note: The document states "Result" and lists "Pass" for each test. The implicit acceptance criterion for each test is that the device must "Pass". Specific quantitative acceptance ranges (e.g., "tensile strength > X N") are not detailed in this summary document.

    2. Sample size used for the test set and the data provenance: Not applicable. This document describes bench testing of a physical medical device, not a performance study of an AI/software device using a test set of data.

    3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts: Not applicable. Ground truth, in the context of expert review for AI performance, is not relevant to bench testing of a guidewire.

    4. Adjudication method (e.g. 2+1, 3+1, none) for the test set: Not applicable.

    5. If a multi reader multi case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance: Not applicable. This is not an AI/software device.

    6. If a standalone (i.e. algorithm only without human-in-the-loop performance) was done: Not applicable. This is not an AI/software device.

    7. The type of ground truth used (expert consensus, pathology, outcomes data, etc.): The "ground truth" for the bench tests would be the established engineering specifications and performance standards for guidewires, against which the device's physical attributes and mechanical properties were measured.

    8. The sample size for the training set: Not applicable. This is not an AI/software device.

    9. How the ground truth for the training set was established: Not applicable. This is not an AI/software device.

    Summary of the Study Proving Device Meets Acceptance Criteria:

    The study proving the device meets the acceptance criteria is detailed in the "Verification and Test Summary Table" provided in the document. This section lists various bench tests conducted on the Traxcess 14EX Guidewire and Traxcess Docking Wire.

    Study Type: Bench Testing

    Objective: To demonstrate the technological similarity and equivalency of the Traxcess 14EX Guidewire and Traxcess Docking Wire with predicate devices by verifying its physical and mechanical properties.

    Methods: The device underwent a series of standard bench tests that assessed critical performance characteristics for a guidewire. These tests included:

    • Physical attributes
    • Distal tip tensile strength
    • Tip flexibility
    • Distal tip torque strength
    • Coating adherence
    • Torqueability
    • Attachment with docking wire
    • Docking wire tensile strength

    Results: For all listed bench tests, the device "Passed," indicating that it met the pre-defined (though not explicitly detailed in quantitative terms in this summary) acceptance criteria for each test.

    Conclusion: Based on these successful bench test results, the submission concludes that the Traxcess 14EX Guidewire and Traxcess Docking Wire are substantially equivalent to the predicate devices, sharing the same intended use, operating principle, basic design, similar construction and materials, and using the same packaging and sterilization processes.

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