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510(k) Data Aggregation

    K Number
    K961847
    Date Cleared
    1997-01-22

    (254 days)

    Product Code
    Regulation Number
    870.3450
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K954848

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

    For use in systemic vascular reconstructions, e.g., replacement in the case of aneurysmal or occlusive disease, in the peripheral region.

    Device Description

    The HEMASHIELD VANTAGE™ Vascular Graft is a woven polyester graft, impregnated with bovine collagen.

    AI/ML Overview

    The provided text describes a medical device, the HEMASHIELD VANTAGE™ Vascular Graft, and its substantial equivalence to predicate devices, but it does not contain information about acceptance criteria or a study proving the device meets those criteria in the context of an AI/ML or diagnostic device.

    The document details product testing for physical and material properties of the graft (e.g., Burst Strength, Tensile Strength, Integral Water Permeability) to demonstrate equivalence to predicate devices. It also mentions biocompatibility testing. However, these are engineering and material science tests, not performance studies for an AI/ML diagnostic system or a study with a test set, ground truth, or expert readers.

    Therefore, I cannot fulfill the request to describe acceptance criteria and a study proving the device meets them, as the provided text pertains to a different type of medical device assessment.

    Here's a breakdown of why the requested information cannot be extracted from the given text:

    • No AI/ML or Diagnostic Device: The HEMASHIELD VANTAGE™ Vascular Graft is a physical vascular graft for surgical replacement, not a diagnostic tool or an AI/ML system.
    • No Acceptance Criteria for Diagnostic Performance: The "acceptance criteria" discussed in the text are implicitly related to the physical and chemical properties of the graft meeting established standards for similar devices, not to diagnostic performance metrics like sensitivity, specificity, or AUC.
    • No "Study" in the Requested Sense: The "testing" mentioned (Burst Strength, Tensile Strength, etc.) are laboratory characterizations of a physical product, not clinical or reader studies involving patient data, ground truth, or human expert interpretation.
    • No Test Set, Ground Truth, or Expert Readers: These concepts are entirely absent because the device is not a diagnostic or AI system.
    • No MRMC or Standalone Performance: These are metrics specific to AI/ML diagnostic device evaluation.
    • No Training Set: As it's a physical product, there's no training set in the context of machine learning.
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