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510(k) Data Aggregation

    K Number
    K984241
    Device Name
    ROCS ULTRASEED
    Date Cleared
    1999-05-12

    (166 days)

    Product Code
    Regulation Number
    892.5050
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K862643

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

    ROCS ULTRASEED™ (Prostate Ultrasound-guided Brachytherapy Planning System) is intended to be used for the computation, display, evaluation and output documentation of radiation dose estimations for prostate ultrasound-guided brachytherapy to be submitted for independent clinical review and judgment. The goal of this system is to provide a tool that will provide consistent results using well documented algorithms. This system does not provide direct or indirect control over any treatment delivery device or system in any form. The device only provides output data in the form of displays, hardcopy prints and/or plots to guide a physician in selecting the optimum patient treatment plan and for documenting the actual implant. It is intended to provide a report to be used by a competent health professional such as a radiation oncologist, medical physicist, radiation therapist or dosimetrist.

    Device Description

    ROCS Ultraseed is software that executes well known and documented algorithms to produce radiation dose estimations for prostate ultrasound-guided brachytherapy. All data is user controlled and is in a table look-up format. Information is presented graphically on CRT screens and in hardcopy reports. The software is designed to run on a PC platform utilizing the Microsoft® Windows® operating systems. All dates are four digit numbers so the system is able to handle the year 2000.

    AI/ML Overview

    I am sorry, but the provided text does not contain information about acceptance criteria, device performance, study details, or ground truth establishment. The document is primarily a 510(k) summary and an FDA clearance letter for the ROCS Ultraseed™ device, focusing on its intended use, technological characteristics, and substantial equivalence to a predicate device. It lacks the specifics requested regarding a study proving the device meets acceptance criteria.

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