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510(k) Data Aggregation

    K Number
    K034051
    Manufacturer
    Date Cleared
    2004-04-05

    (97 days)

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

    DYNATRAC, COD. 50-1A

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

    It is intended for localization of patient position in the conduct of radiation therapy with a linear accelcrator and registration of patient position between the planning and conduct of treatment. Patient Tracking System is an optical system for tracking patient position to linear accelerators used for before and during facilomeraly. It is an accessory of 3 dimensional radiotherapy.

    Device Description

    DynaTrac System Cod. 50-1A is a state-of-the-art optical tracking system that tracks patient position before and during a radiotherapy treatment session. It can track the patient in real time allowing the treatment system to respond to uncxpected movements. It shortens the time required to prepare a patient for a treatment session because of the speed with which spatial registration with a treatment plan can be confirmed.

    AI/ML Overview

    The provided text is a 510(k) summary for the DynaTrac System, an optical patient tracking system for radiation therapy. It establishes substantial equivalence to a predicate device (ExacTrac) but does not contain any information about specific acceptance criteria, study designs, or performance metrics from a validation study.

    Therefore, I cannot provide the requested information in a table or as descriptive text regarding the acceptance criteria and a study proving the device meets them. The document focuses on regulatory approval based on demonstrating substantial equivalence, not on presenting performance data from a specific study.

    The document only states: "DynaTrac has the same intended use and Davoluntial Dquiraliso to ExacTrac. There are no technical differences that raise issues of safety and effectiveness." This implies that the device is considered equivalent based on its design and intended use being similar to a legally marketed device, not through a new performance study detailed in this submission.

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