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510(k) Data Aggregation

    K Number
    K032360

    Validate with FDA (Live)

    Date Cleared
    2003-08-27

    (27 days)

    Product Code
    Regulation Number
    876.5010
    Age Range
    All
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Boston Scientific Express™ Biliary LD Stent is indicated for the palliation of malignant neoplasms in the biliary tree.

    Device Description

    The 5 mm Express Biliary LD Stent (Premounted Stent System and Unmounted Stent) are identical to the currently marketed Express Biliary LD Premounted Stent Systems (K021630 and K024048) and to the currently marketed Express Biliary LD Unmounted Stents (K030645), with the exception of size. The Express Biliary LD Stent is a balloon expandable 316L surgical grade stainless steel stent intended to maintain patency of biliary strictures produced by malignant neoplasms. The stent will be available in a variety of sizes to address clinician needs.

    AI/ML Overview

    The provided text describes a 510(k) summary for the Boston Scientific Express Biliary LD Stent and explicitly states the device's substantial equivalence to predicate devices based on non-clinical testing. It does not contain information about acceptance criteria, device performance via a clinical study, sample sizes, expert involvement, adjudication methods, MRMC studies, or standalone algorithm performance. The information focuses on design, manufacturing, and intended use equivalence, referencing existing 510(k) applications for a detailed device description.

    Therefore, I cannot fulfill your request for information regarding clinical study setup and results from the provided text. The document is a regulatory submission focused on demonstrating substantial equivalence through non-clinical means.

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