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510(k) Data Aggregation

    K Number
    K073114
    Date Cleared
    2008-01-17

    (73 days)

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

    IMIX INSIGHT X-RAY SYSTEMS

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

    IMIX Insight X-Ray Systems are indicated for use in generating radiographic images of human anatomy. It has a Solid State X-ray Imaging system intended to replace radiographic film/screen systems in all general-purpose diagnostic procedures. IMIX Insight X-Ray Systems are not indicated for diagnostic X-ray mammography.

    Device Description

    System Features

    • URS Radiographic Stand .
    • Fully motorized movements with intelligent anti-collision system .
    • Automatic settings for 40 and 72 inch SID, auto-position for table exposures .
    • Patient Table capacity of 440 lbs .
    • Collimator with light field and laser positioning .
    • X-Ray Subsystem 65 kW High Frequency Compact Generator .
    • Full Anatomical Programming .
    • Automatic Exposure Control .
    • High Capacity (300kHU) X-ray tube with 0.6/1.2mm focus (27/75kW) .
    • Microprocessor System Monitor .
    • IMIX Insight Detector: High Resolution 9 megapixel or 16 megapixel CCD detector .
    • 40cm x 40cm Image Format (16 x 16 inch) .
    • Spatial Resolution: >3.1 1p/mm (4Mp) or >4.3 1p/mm (16Mp) .
    • Image Acquisition: 16 bit .
    • 3 Field Ionization Chamber .
    AI/ML Overview

    The provided text (K073114) describes an X-ray system called the IMIX Insight X-Ray System. However, it does not contain information about acceptance criteria or a study proving that the device meets those criteria.

    The document is a 510(k) summary, which focuses on demonstrating substantial equivalence to a legally marketed predicate device, rather than providing detailed performance studies against specific acceptance criteria.

    Therefore, I cannot provide the requested information from the given text. The text does not include:

    1. A table of acceptance criteria and reported device performance.
    2. Sample sizes used for test sets or data provenance.
    3. Number of experts or their qualifications for establishing ground truth.
    4. Adjudication methods.
    5. Information about MRMC comparative effectiveness studies or effect sizes.
    6. Information about standalone algorithm performance studies.
    7. The type of ground truth used.
    8. The sample size for the training set.
    9. How ground truth for the training set was established.

    The document primarily states:

    • Device Name: IMIX Insight X-Ray Systems
    • Intended Use: Generating radiographic images of human anatomy, replacing radiographic film/screen systems in general-purpose diagnostic procedures. Not indicated for diagnostic X-ray mammography.
    • Substantial Equivalence: The device is a modified combination of a cleared device (IMIX Digital Thorax K974863) with exempt devices, and is functionally identical to the SEDECAL URS LP X-Ray Units with Digital Detector (K042876) and similar to Vidar Vision 3000 and 4000 (K071193).
    • Device Description: Provides details about system features like the URS Radiographic Stand, X-Ray Subsystem, and IMIX Insight Detector specifications (e.g., 9 or 16 megapixel CCD detector, 40cm x 40cm image format, spatial resolution >3.1 lp/mm or >4.3 lp/mm, 16-bit image acquisition).
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