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510(k) Data Aggregation

    K Number
    K093291
    Date Cleared
    2009-11-17

    (27 days)

    Product Code
    Regulation Number
    892.5700
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    VARIAN INTERSTITIAL TITANIUM NEEDLES

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

    The Interstitial Needles are used with Varian High Dose Rate Afterloaders.

    Device Description

    The device is a family of closed-ended, interstitial needles and associated obturators to be used in conjunction with a high dose rate (HDR) brachytherapy afterloading device. The needles are available in either 17 gauge O.D. or 18 gauge O.D. and in lengths of 113mm, 200 mm, 250mm and 320mm. The associated obturators are inserted into needles to stiffen the needles during implantation of the needles into the patient and to stiffen the needles between radiation therapy fractions. The obturators are available in lengths of 113mm, 200 mm, 250mm and 320mm. The needles are provided unsterile with instructions for steam sterilization. The obturators are provided unsterile with instructions for steam sterilization.

    AI/ML Overview

    The provided document is a 510(k) Premarket Notification for "Varian Interstitial Needles." This type of document is for medical devices and focuses on demonstrating substantial equivalence to a predicate device, rather than conducting new clinical studies with detailed acceptance criteria and performance evaluation against those criteria in the way a diagnostic AI device would.

    Therefore, the document does not contain the information requested in your prompt regarding acceptance criteria, study details, sample sizes, expert involvement, or comparative effectiveness studies. The provided text is a regulatory submission for a physical medical device (needles) and not an AI or software-as-a-medical-device (SaMD) product that would typically involve such detailed performance studies.

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