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510(k) Data Aggregation

    K Number
    K202713
    Device Name
    TrueView 100 Pro
    Date Cleared
    2020-11-18

    (63 days)

    Product Code
    Regulation Number
    892.1680
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    TrueView 100 Pro

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

    A cabinet X-ray system used to provide digital X-ray images of surgical and core biopsy specimens from various anatomical regions in order to allow rapid verification that the correct tissue has been excised during the biopsy procedure.

    Doing the verification in the same room as the procedure or nearby improves workflow, thus reducing the time the patient needs to be under examination.

    Device Description

    The TrueView 100 Pro is a self-contained, direct digital imaging system for imaging surgical and biopsy specimens. The TrueView 100 Pro includes the following major components: a system monitor, touch-screen display, a touchpad, and an imaging cabinet. The system is self-contained. Shielding is incorporated within the cabinet chamber system design, eliminating the need for separate shielding. The unit is mounted on casters to allow for easy transportation.

    AI/ML Overview

    This document, a 510(k) Premarket Notification Summary for the TrueView 100 Pro Specimen Radiography System, primarily focuses on demonstrating substantial equivalence to a predicate device rather than providing a detailed study proving the device meets specific acceptance criteria with quantifiable metrics.

    The information provided does not include:

    • A table of acceptance criteria with reported device performance.
    • Specific sample sizes for test sets, data provenance, or details about ground truth establishment for a test set.
    • Information on the number or qualifications of experts, or adjudication methods for ground truth in a test set.
    • Details of a multireader multicase (MRMC) comparative effectiveness study or standalone algorithm performance.
    • Sample size for a training set or how ground truth for a training set was established.

    Instead, the submission relies on comparing the technical specifications and performance characteristics of the TrueView 100 Pro to its predicate device, the Trident® HD Specimen Radiography System (K182727), to argue for substantial equivalence.

    Here's an analysis of the information available in the provided text:

    1. A table of acceptance criteria and the reported device performance:

    The document provides a comparative table between the TrueView 100 Pro and the predicate device. While this table lists various technical specifications and operational parameters, it does not explicitly define acceptance criteria for each parameter and then report the TrueView 100 Pro's performance against those criteria. Instead, it compares the TrueView 100 Pro's specifications directly to the predicate's specifications to demonstrate "similarity" or "improvement."

    Here's a summary of the technical comparison presented in the document, which can be interpreted as the basis for performance claims relative to the predicate:

    FeaturePredicate (Trident® K182727)TrueView 100 Pro (Proposed)Comparison
    Indications for UseSame as proposedA cabinet X-ray system for digital X-ray images of surgical and core biopsy specimens to verify tissue removal. Improves workflow by reducing patient examination time.Same
    Principle of OperationX-ray imaging principleX-ray imaging principleSame
    Level of ConcernModerateModerateSame
    Method of UseCabinet X-ray system for imaging small to large biopsy and surgical specimensCabinet X-ray system for imaging small to large biopsy and surgical specimensSame
    Mechanism of ActionSample verification: obtain correct margins, specimen of interest, etc.Sample verification: obtain correct margins, specimen of interest, etc.Same
    Physical ConstructionFully integrated system with movable base castersFully integrated system with movable base castersSimilar; designed for ease of use and transportation
    Size (W x D x H)24 x 26 x 66.5 (in.)23.6 x 28.3 x 64.9 (in.)Similar: slim design for ease of use and transportation
    Detector TechnologyTFT-based direct capture technologyActive-pixel CMOSDifferent
    Active Imaging Area12 cm x 14 cm (MFD), 20 cm x 20 cm (HDT)11.4 cm x 14.6 cmTrident® HD is available with two detectors; TrueView has one size.
    Pixel Size70 µm pixels49.5 µm pixelsSimilar, TrueView 100 Pro pixel size is 29% smaller
    Limiting Spatial Resolution7.1 lp/mm10 lp/mmSimilar, TrueView 100 Pro has 41% more line pairs per mm.
    Output Image14-bit image data14-bit image dataSame
    Display Monitor2 MP High luminescence diagnostic monitor2.3 MP High luminescence diagnostic monitorSimilar, TrueView 100 Pro slightly improved resolution
    Operating SystemWindows 10Windows 10Same
    User InterfaceIntegrated touch screen, track padIntegrated touch screen, track padSame
    Energy Range20-50 kV20-50 kVSame
    Anode TypeTungstenTungstenSame
    Tube Current1 mA1 mASame
    ExposureUp to 20 mAsUp to 20 mAsSame
    Focal Spot Size50 µm50 µmSame
    Exposure ModesManual (User selects kV and mAs), Auto (System determines optimum kV and mAs)Manual (User selects kV and mAs), Auto (System determines optimum kV and mAs)Same
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