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510(k) Data Aggregation

    K Number
    K000540
    Date Cleared
    2000-04-27

    (70 days)

    Product Code
    Regulation Number
    878.5000
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    POLYESTER NONABSORBABLE SURGICAL SUTURES, USP

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    Device Description
    AI/ML Overview
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    K Number
    K961925
    Date Cleared
    1996-07-29

    (73 days)

    Product Code
    Regulation Number
    878.5000
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    POLYESTER NONABSORBABLE SURGICAL SUTURES USP

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

    The polyester nonabsorbable surgical sutures USP are indicated for use in general soft tissue approximation and/or ligation including use in cardiovascular, ophthalmic and neurological procedures.

    Device Description

    Polyester nonabsorbable surgical sutures USP, manufactured by R.K. Medical, L.L.C. are equivalent to Ti-cron* polyester nonabsorbable surgical suture USP manufactured by Davis & Geck. The polyester nonabsorbable surgical sutures USP manufactured by R.K. Medical and Davis & Geck are braided and coated with silicone. The R.K. Medical polyester suture is dyed green (D&C Green #6). Davis & Geck's Ti-cron* is dyed blue (D&C Blue #6).

    AI/ML Overview

    Here's an analysis of the provided text regarding acceptance criteria and device performance:

    This document describes a 510(k) submission for a medical device, but it fundamentally lacks the detailed information required to answer most of your detailed questions about AI device performance and studies. The device described is a Polyester Nonabsorbable Surgical Suture, which is a physical, non-AI medical device. The document predates the widespread use of AI in medical imaging and diagnostics, and thus, its content is focused on traditional medical device equivalency rather than AI performance.

    Therefore, the following answers are based on the limited information provided for a non-AI device.


    1. Table of Acceptance Criteria and Reported Device Performance

    Acceptance CriteriaReported Device Performance (R.K. Medical Polyester Suture)
    Suture DiameterMeets or exceeds USP specifications
    Suture LengthMeets or exceeds USP specifications
    Knot Pull Tensile StrengthMeets or exceeds USP specifications
    Needle Attachment StrengthMeets or exceeds USP specifications

    Additional Note: The document states the R.K. Medical sutures are "equivalent to Ti-cron* polyester nonabsorbable surgical suture USP manufactured by Davis & Geck" in terms of the above parameters.


    Regarding the remaining questions on AI device studies:

    The provided document does not contain any information about an AI-powered device, image analysis, diagnostic algorithms, or any type of study that would involve:

    • AI performance metrics (sensitivity, specificity, AUC)
    • Sample sizes for test or training sets for an AI model
    • Data provenance for AI input data
    • Experts establishing ground truth for AI analysis
    • Adjudication methods for AI
    • Multi-reader multi-case (MRMC) comparative effectiveness studies with AI assistance
    • Standalone (algorithm-only) AI performance studies
    • Types of ground truth for AI (pathology, outcomes)
    • Training set details for AI algorithms

    Therefore, it is impossible to provide answers to questions 2 through 9 based on the given text. This document is for a physical surgical suture, not an AI device.

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