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510(k) Data Aggregation

    K Number
    K052954
    Manufacturer
    Date Cleared
    2006-02-15

    (118 days)

    Product Code
    Regulation Number
    868.5140
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Continuous Stimulating Catheter News Block Set permits placement of catherers next to nerves and nerve plexus for continuous stimulating and analgesia techniques. It is indicated for use up to 72 hours.

    Device Description

    ContiStim Continuous Stimulating Catheter Nerve Block Set

    AI/ML Overview

    The provided document is a 510(k) clearance letter from the FDA for a device called "ContiStim Continuous Stimulating Catheter Nerve Block Set." It indicates that the device has been found substantially equivalent to legally marketed predicate devices.

    However, this document does not contain information about acceptance criteria or a study proving the device meets acceptance criteria. It is a regulatory approval document confirming substantial equivalence, not a summary of performance testing or clinical trial results.

    Therefore, I cannot provide the requested information from this document. The sections you asked for, such as "Table of acceptance criteria and reported device performance," "Sample size used for the test set," "Number of experts used," "Adjudication method," "MRMC comparative effectiveness study," "Standalone performance," "Type of ground truth," "Sample size for the training set," and "How ground truth for training set was established," are not present in this regulatory clearance letter.

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