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510(k) Data Aggregation

    K Number
    K102011
    Date Cleared
    2010-09-03

    (49 days)

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

    K091492

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

    The Eclipse Treatment Planning System (Eclipse TPS) is used to plan radiotherapy treatments for patients with malignant or benign diseases. Eclipse TPS is used to plan external beam irradiation with photon, electron and proton beams, as well as for internal irradiation (brachytherapy) treatments. In addition, the Eclipse Proton Eye algorithm is specifically indicated for planning proton treatment of neoplasms of the eye.

    Device Description

    The Varian Eclipse™ Treatment Planning System (Eclipse TPS) provides software tools for planning the treatment of malignant or benign diseases with radiation. Eclipse TPS is a computerbased software device used by trained medical professionals to design and simulate radiation therapy treatments. Eclipse TPS is capable of planning treatments for external beam irradiation with photon, electron, and proton beams, as well as for internal irradiation, (brachytherapy) treatments.

    AI/ML Overview

    The provided text describes the Eclipse Treatment Planning System (Eclipse TPS) and compares its features to a predicate device. However, it does not contain a study or data proving the device meets specific acceptance criteria in the context of a clinical performance evaluation.

    Instead, the document is a Premarket Notification 510(k) Summary for the Eclipse TPS, which focuses on demonstrating substantial equivalence to a legally marketed predicate device. This is a regulatory submission process, not a clinical study.

    Here's a breakdown of why the requested information cannot be fully provided from the given text:

    • No "Acceptance Criteria" as clinical performance metrics: The table presented in the document is a "Substantial Equivalence Comparison Chart" which outlines features and functionalities of the Eclipse TPS and compares them to its predicate device. These are design and functional specifications, not clinical acceptance criteria with performance targets (e.g., sensitivity, specificity, accuracy, or reader agreement).
    • No "Study" in the sense of a clinical trial: The document does not describe any clinical study, experimental design, or results that evaluate the device's performance against clinical endpoints. The "study" mentioned here refers to the 510(k) submission process itself, which relies on demonstrating equivalence rather than proving de novo clinical performance.

    Therefore, for aspects related to "acceptance criteria," "study," "sample size," "experts," "ground truth," "MRMC," and "standalone performance," the information is not available in the provided text.

    Here's what can be extracted based on the nature of the document:


    1. Table of Acceptance Criteria and Reported Device Performance

    As explained above, the provided document does not present clinical acceptance criteria with performance metrics. Instead, it provides a "Substantial Equivalence Comparison Chart" detailing functional specifications and comparing the proposed device (Eclipse TPS) to a predicate device (Eclipse Treatment Planning System, K091492).

    Feature/CharacteristicAcceptance Criteria (Predicate)Reported Device Performance (Eclipse TPS)
    Indication for UseSee aboveSee above
    General Usage
    External beam PHOTON planningyesyes
    External beam PHOTON inverse planningyesyes
    External beam ELECTRON planningyesyes
    External beam PROTON planningyesyes
    External beam OCULAR PROTON planningyesyes
    Internal BRACHYTHERAPY planningyesyes
    Stereotactic Frame Localizationyesyes
    Supported External Beams & Accessories
    Photon beamsyesyes
    Electron beamsyesyes
    Proton beamsyesyes
    Coplanar fieldsyesyes
    Non-coplanar fieldsyesyes
    Multi-leaf Collimatorsyesyes
    Asymmetric collimatorsyesyes
    Stereotactic Cone collimatorsyesyes
    Arc fieldsyesyes
    Poured Blocksyesyes
    Compensatorsyesyes
    Physical wedgesyesyes
    Dynamic wedgesyesyes
    Rotating treatment couchyesyes
    Supported Brachytherapy Sources & Accessories
    Plan for high dose rate afterloaderyesyes
    Manual low dose rate brachytherapy:
    seeds, line sources, wireyesyes
    Applicator libraryyesyes
    Needle templatesyesyes
    Graphical User Interface
    Multiple-instance applicationyesyes
    Multiple-workspace layoutyesyes
    Graphical display/editing of field parametersyesyes
    Beam's-Eye-View displayyesyes
    3D patient image displayyesyes
    Model for human Eyeyesyes
    SRS Localization applicationyesyes
    SRS Planning applicationyesyes
    Biological Optimization applicationyesyes
    Biological Evaluation applicationyesyes
    3D Conformal Optimization applicationyesyes
    Image Processing
    Orthogonal image displays (3)yesyes
    Oblique image displayyesyes
    Edge enhancement filtersyesyes
    Image smoothing filtersyesyes
    CT/MR/PET Image Registrationyesyes
    Image blending utilityyesyes
    4D image display (registration of time series of 3D images)yesyes
    Digitally reconstructed radiographsyesyes
    Enclosed Volume measurementyesyes
    Stereotactic Frame Coordinate transformationyesyes
    Image Segmentation
    Geometrical shapesyesyes
    Manual editing and manipulation toolsyesyes
    Automatic /semi-automatic toolsyesyes
    Automatic/semi-automatic on-demand and post-processing tools for individual organs/structuresyesyes
    Automatic on-demand and pre-processing tools for multiple organs/structuresyesyes
    3D Automarginyesyes
    Logical operatorsyesyes
    Dose Calculation
    Distributed Calculation Frameworkyesyes
    Photon calculationyesyes
    Energy Range (Photon)1 MV - 50 MV1 MV - 50 MV
    CT-based volumetric calculationyesyes
    Non-CT based IRREG calculationyesyes
    Convolution methodyesyes
    Combined electron/photon scatteryesyes
    Directional heterogeneity correctionyesyes
    Treatment head modelingyesyes
    Photon Monitor Unit calculationyesyes
    Beam Angle Optimization (GEOS)yesyes
    Leaf Motion Sequencingyesyes
    Dose Dynamic Arc planningyesyes
    Cone Dose Calculationyesyes
    Biological optimizationyesyes
    3D Conformal Optimizationyesyes
    AcurosXB dose calculation algorithmnoyes
    Electron calculationyesyes
    Energy Range (Electron)1 MeV - 50 MeV1 MeV - 50 MeV
    Gaussian Pencil Beam Modelyesyes
    Electron Monte Carlo algorithmyesyes
    Electron Monitor Unit calculationyesyes
    Proton calculationyesyes
    Energy Range (Proton)50 MeV - 300 MeV50 MeV - 300 MeV
    Brachytherapy calculationyesyes
    AAPM TG 43 compliantyesyes
    Point Dose calculationyesyes
    Optimization to point dose constraintsyesyes
    Geometric optimizationyesyes
    Acuros dose calculation algorithmyesyes
    Eclipse Algorithm Application Programming Interface (EAAPI)noyes
    Dose Evaluation
    Dose color wash2D, 3D2D, 3D
    Isodose levels2D, 3D2D, 3D
    Isodose Surface3D3D
    Reference point dose summaryyesyes
    Dose Volume Histogram plotyesyes
    Plan summing toolyesyes
    Plan comparison toolsyesyes
    Evaluation using biological modelsyesyes
    Plan Output - Hardcopy
    Graphics window screen dumpyesyes
    Patient administration datayesyes
    Plan parametersyesyes
    Geometrical displays of plan datayesyes
    Dose distributionyesyes
    DVH plotyesyes
    BEV displayyesyes
    Patient orientationyesyes
    User Configurable hardcopy layoutsyesyes
    Import/Export Interfaces
    VARIS/Vision database integrationyesyes
    DICOM RT / 3.0yesyes
    Other image formatsyesyes
    Electromagnetic Digitizerimportimport
    Film Scannerimportimport
    Export field coordinates to Laser Systemexportexport

    2. Sample size used for the test set and the data provenance:

    • Sample size: Not applicable/not provided. This document doesn't describe a clinical test set or study.
    • Data provenance: Not applicable/not provided.

    3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts:

    • Not applicable/not provided.

    4. Adjudication method for the test set:

    • Not applicable/not provided.

    5. If a multi reader multi case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance:

    • No MRMC study was done/reported in this document. The device is a treatment planning system, not an AI-assisted diagnostic device for human readers.

    6. If a standalone (i.e. algorithm only without human-in-the loop performance) was done:

    • Not applicable/not provided as a standalone performance study. The document focuses on the functional equivalence of the entire system for treatment planning, which inherently involves human professional users.

    7. The type of ground truth used:

    • Not applicable/not provided in the context of a performance study. For regulatory purposes, the "ground truth" for substantial equivalence is the predicate device's established performance and specifications.

    8. The sample size for the training set:

    • Not applicable/not provided. This document is not describing a machine learning or AI algorithm development study that would involve a training set.

    9. How the ground truth for the training set was established:

    • Not applicable/not provided.
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