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510(k) Data Aggregation

    K Number
    K081060
    Date Cleared
    2008-12-24

    (254 days)

    Product Code
    Regulation Number
    878.4495
    Reference & Predicate Devices
    N/A
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    ferroFibre 14 Stainless Steel Sutures are intended for use in soft tissue approximation and for use in abdominal wound closure, hernia repair, sternal closure and certain orthopaedic procedures including cerclage and tendon repair.

    Device Description

    The ferroFibre™ Stainless Steel Suture is available in United States Pharmacopocia (USP) sizes 5-0 to #5 in various lengths. The ferroFibre multifilament stainless stecl sutures are supplied storile, armed with cutting needles. The sutures are fabricated from 316 stainless steel that meets ASTM F138-03.

    AI/ML Overview

    The provided text describes a 510(k) submission for the ferroFibre™ Stainless Steel Suture. This document focuses on the regulatory clearance for a medical device and does not contain information about an AI/ML powered device, nor does it detail a clinical study with acceptance criteria and reported device performance in the way requested.

    The document outlines performance testing conducted to characterize biocompatibility, diameter, and tensile strength according to ISO 10993 standards and USP Monographs. However, it does not provide specific acceptance criteria or reported performance values for these tests. It also does not include details on sample sizes for testing, ground truth establishment, expert involvement, or any multi-reader multi-case (MRMC) studies, as these types of studies are not relevant for the regulatory approval of a non-AI/ML surgical suture device.

    Therefore, I cannot populate the requested table or answer the specific questions related to AI/ML device performance and clinical study design for this submission. The content is about a traditional medical device (surgical sutures) and its regulatory clearance based on substantial equivalence to existing products.

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