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510(k) Data Aggregation

    K Number
    K060679
    Date Cleared
    2006-04-21

    (37 days)

    Product Code
    Regulation Number
    892.5730
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    SURTRAK IMPLANTATION KIT

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

    The North American Scientific, Inc Brachytherapy Preloaded Needle Kit is indicated for interstitial implantation of select localized tumors with low to medium radiosensitivity. They are used either as primary treatment for tumors such as those in the head, neck, lung, pancreas, breast, cervix and prostate and unresectable turnors or for residual disease after excision of the primary turnor. North American Scientific Brachytherapy Preloaded Needle Kit implants are indicated for use with or at the completion of other treatment modalities, such as external beam radiation therapy or chemotherapy.

    Device Description

    Not Found

    AI/ML Overview

    I am sorry, but the provided text does not contain the information requested in your prompt. The document is a 510(k) clearance letter from the FDA for a medical device called the "Surtrak® Implantation Kit". It primarily addresses regulatory aspects, substantial equivalence to predicate devices, and indications for use.

    It does not include:

    • A table of acceptance criteria and reported device performance.
    • Details about sample sizes, data provenance, or the type of study conducted.
    • Information on ground truth establishment, expert qualifications, or adjudication methods.
    • Data on Multi-Reader Multi-Case (MRMC) studies or standalone algorithm performance.
    • Training set details or how their ground truth was established.

    Therefore, I cannot fulfill your request using the provided input.

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