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510(k) Data Aggregation

    K Number
    K203010
    Manufacturer
    Date Cleared
    2021-01-22

    (113 days)

    Product Code
    Regulation Number
    892.1650
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    Platinum dRF Imaging System

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

    The Platinum dRF Imaging System is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic studies. Using a digital flat detector, it can perform a range of applications including: general radiology and diagnostic fluoroscopy examinations, conventional linear tomography and pediatrics examinations.

    The Platinum dRF is a device intended to visualize anatomical structures by converting a pattern of X-ray into a visible image. The system has medical applications ranging from, but not limited to, gastrointestinal, cranial, skeletal, thoracic, lung and urogenital tract examinations.

    It may also be used in: lymphography, endoscopy, myelography, venography and arthrography.

    The Platinum dRF may also be used for outpatient or emergency services, as well as for mobile transport examinations (wheelchair and bed).

    The Platinum dRF is not indicated for use in interventional radiology.

    Device Description

    The subject of this Special 510(k) application is the change to the imaging software system to the ADAM Imaging System. As the resources are now available, Apelem-DMS Group was able to develop their own Imaging System called the ADAM Imaging System. The ADAM Imaging System will now be developed by Apelem-DMS Group. The predicate device (K160301) had an Off the Shelf Software Imaging System called DUET DRF Imaging System which was developed by Thales.

    The ADAM Imaging System is a digital image acquisition system to be used in conjunction with a detector during radiography or fluoroscopy X-ray examinations to acquire, display, process and export images according to DICOM protocol via a network connection.

    The ADAM Imaging System software interfaces with an X-Ray detector to acquire raw pixel data and image processing algorithms which transform raw pixel data into images and image sequences to help medical professionals with viewing images to for patient diagnosis.

    The Duet DRF requires the use of the THALES RF4343 FL detectors, whereas ADAM Imaging System requires the use of the VIEWORKS VIVIX-D 1717G detector. Both detectors employ the same state-of-the-art indirect conversion technology based on CsI scintillator and photo-diodes. The detector Vivix-D 1717G is connected to the x-ray system by cable. The integration with the PLATINUM dRF system has been established and appears adequate. The VIEWWORKS VIVIX-D 1717G detector is only compatible with the ADAM Imaging System.

    The Duet DRF and ADAM Imaging System are designed to support general radiography (excluding mammography) and fluoroscopy imaging procedures.

    The Apelem-DMS Group ADAM Imaging System is not a stand-alone device. It is integrated into the Platinum dRF Imaging System and functions as a platform for FDA cleared or registered components (i.e. generator, panel detector, detector collimator, X-ray tube and software imaging packages), that are installed with a Apelem-DMS Group manufactured radiological examination table, control panel with system controller software, and electrical panel.

    The Platinum dRF remote controlled table is a radiologic table equipped with a flat panel electronic detector. This table is used to perform general digital radiological, fluoroscopy and peripheral angiography.

    AI/ML Overview

    The provided document is a 510(k) summary for the Platinum dRF Imaging System and does not contain detailed information about acceptance criteria or a study proving that the device meets those criteria. The document states that the new ADAM Imaging System component changes the internal imaging software and detector, but it does not include performance data or explicit acceptance criteria for image quality, diagnostic accuracy, or clinical effectiveness.

    The submission focuses primarily on demonstrating substantial equivalence to a predicate device (K160301) by comparing technical specifications and highlighting that the proposed changes do not raise new questions of safety or effectiveness. It mentions compliance with various IEC and ISO standards related to medical electrical equipment, software, and risk management, which are general safety and performance standards rather than specific acceptance criteria for a diagnostic imaging study.

    Therefore, most of the requested information regarding acceptance criteria and performance study details cannot be extracted from this document.

    However, based on the available information, here's what can be inferred:

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

    • Acceptance Criteria: Not explicitly stated in terms of measurable performance metrics for a diagnostic study. The document primarily focuses on demonstrating that the performance of the new detector (VIEWORKS VIVIX-D 1717G) is "similar enough" or "sufficient" compared to the predicate's detector.
    • Reported Device Performance: The document provides technical specifications of the new detector and compares them to the predicate's detector, implying these are the performance characteristics considered.
    MetricAcceptance Criteria (Implied)Reported Device Performance (ADAM Imaging System Detector)Reported Predicate Performance (DUET Imaging System Detector)Comment
    ScintillatorSame as predicateCsICsISame
    Pixel PitchSimilar to predicate; smaller is generally better140µm148µmADAM Imaging System's detector has a smaller pixel pitch which means better detail detectability.
    Pixel MatrixSimilar to predicate; larger is generally better3072 x 3072 pixels2874 x 2840 pixelsAdam Imaging System's detector has a larger pixel matrix which means a larger detection field.
    Image SizeSame as predicate17" x 17"17" x 17"Same
    GrayscaleSame as predicate16 bits16 bitSame
    ResolutionPerformance similar enough (>3%) for indicated procedures3.5 linepairs/mm3.4 linepairs/mmThe performance of both detectors are similar enough (>3%) for the procedures indicated.
    Modulation Transfer Function (MTF)Performance of both detectors sufficient for general radiographic proceduresMTF IEC 0.5 lp/mm: Minimal 78%, Typical 83%
    MTF IEC 1 lp/mm: Minimal 50%, Typical 55%
    MTF IEC 2 lp/mm: Minimal 20%, Typical 25%
    MTF IEC 3 lp/mm: Minimal 5%, Typical 10%MTF IEC 0.5 lp/mm: Minimal 79%, Typical N/A
    MTF IEC 1 lp/mm: Minimal 55%, Typical 66%
    MTF IEC 2 lp/mm: Minimal 25%, Typical 35%
    MTF IEC 3 lp/mm: Minimal 10%, Typical 19%Performance of both detectors are sufficient for general radiographic procedures. (Predicate listed MTF IEC Nyquist as 7% Minimal, 15% Typical)
    Detective Quantum Efficiency (DQE)DQE difference
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    K Number
    K160301
    Manufacturer
    Date Cleared
    2016-03-04

    (29 days)

    Product Code
    Regulation Number
    892.1650
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    Platinum dRF Imaging System

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

    The Platinum dRF Imaging System is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic studies. Using a digital flat detector, it can perform a range of applications including general R/F, diagnostic fluoroscopy, conventional linear tomography, angiography and pediatric examinations.

    The Platinum dRF is a device intended to visualize anatomical structures by converting a pattern of X-ray into a visible image. The system has medical applications ranging from but not limited to gastrointestinal examinations, cranial, skeletal, thoracic and lung exposures as well as examination of the urogenital tract. The units may also be used in lymphography, endoscopy, myelography, venography, pediatrics, arthrography, digital angiography and digital subtraction angiography (DSA).

    The Platinum dRF may be used for outpatient and emergency treatment, as well as for mobile transport (wheelchair and bed) examinations.

    The Platinum dRF is not indicated for use in interventional radiology.

    Device Description

    The Apelem-DMS Platinum dRF Imaging System ("Platinum") is not a stand-alone device, but functions as a platform for FDA cleared or registered components (i.e. generator, panel detector, detector collimator, X-ray tube and software imaging packages), that are installed with a Apelem-DMS manufactured radiological examination table, control panel with system controller software, and electrical panel.

    The Platinum dRF remote controlled table is a radiologic table equipped with a flat panel electronic detector. This table is used to perform general digital radiological, fluoroscopy and peripheral angiography. This device allows for treatment on the whole body, using all angles. It allows the user dynamic acquisition for the whole body, to target the zones to analyze, and to be able to track contrast media.

    The subject of this Special 510(k) application is the additional offering of the Platinum with a different flat panel detector (RF4343 FL) that does not include some less regularly used options (of the FDA cleared Platinum with RF4343 flat panel detector), has lower frames/sec and does not include a lead shield for use with the RF4343 FL is manufactured and installed by DMS. This additional offering is less expensive and will fit the needs of most customers.

    AI/ML Overview

    The provided document is a 510(k) premarket notification for a medical device (Platinum dRF Imaging System) seeking substantial equivalence to a predicate device. It primarily focuses on demonstrating that a new component (a different flat panel detector) does not alter the device's safety or effectiveness.

    Therefore, this document does not contain the information requested regarding specific acceptance criteria for device performance, a study proving the device meets these criteria, sample sizes for test/training sets, expert ground truth establishment, or multi-reader multi-case studies.

    The document states:

    • The subject of this Special 510(k) application is the additional offering of the Platinum with a different flat panel detector (RF4343 FL) that does not include some less regularly used options (of the FDA cleared Platinum with RF4343 flat panel detector), has lower frames/sec and does not include a lead shield for use with the RF4343 FL is manufactured and installed by DMS.
    • There is no change in the Indications for Use.
    • The change in frame rate has no impact on image quality as the image specifications are not changes.
    • The results of assessment under Design Controls supports that the Apelem-DMS Platinum dRF Imaging System with RF434FL flat panel detector is substantially equivalent to the predicate device. The differences between the RF4343 FL flat panel detector do not raise different issues of safety or effectiveness.
    • The Platinum with RF4343 FL has no impact on the image quality or safety of the device, and does not raise different issues of safety or effectiveness.

    This indicates that the submission relies on the previous clearance of the predicate device (K131766) and argues that the minor changes to the flat panel detector do not necessitate new performance studies or acceptance criteria beyond demonstrating continued compliance with general safety and performance standards for X-ray equipment.

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    K Number
    K131766
    Manufacturer
    Date Cleared
    2013-12-12

    (178 days)

    Product Code
    Regulation Number
    892.1650
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    PLATINUM DRF IMAGING SYSTEM

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

    The Platinum dRF Imaging System is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic studies. Using a digital flat detector, it can perform a range of applications including general R/F, diagnostic fluoroscopy, conventional linear tomography, angiography and pediatric examinations.

    The Platinum dRF is a device intended to visualize anatomical structures by converting a pattern of X-ray into a visible image. The system has medical applications ranging from but not limited to gastrointestinal examinations, cranial, skeletal, thoracic and lung exposures as well as examination of the urogenital tract. The units may also be used in lymphography, endoscopy, myelography, venography, pediatrics, arthrography, digital angiography and digital subtraction angiography (DSA).

    The Platinum dRF may be used for outpatient and emergency treatment, as well as for mobile transport (wheelchair and bed) examinations.

    The Platinum dRF is not indicated for use in interventional radiology.

    Device Description

    The Apelem-DMS Platinum dRF Imaging System (Platinum) is not a stand-alone device, but functions as a platform for FDA cleared or registered components (i.e. generator, panel detector, detector collimator. X-ray tube and software imaging packages), that are installed with a Apelem-DMS manufactured radiological examination table, control panel with system controller software. and electrical panel.

    The Platinum dRF remote controlled table is a radiologic table equipped with a flat panel electronic detector. This table is used to perform general digital radiological, fluoroscopy and peripheral angiography. This device allows for treatment on the whole body, using all angles. It allows the user dynamic acquisition for the whole body, to target the zones to analyze, and to be able to track contrast media.

    AI/ML Overview

    Here's a breakdown of the acceptance criteria and the study information for the Apelem-DMS Platinum dRF Imaging System, based on the provided text:

    Important Note: The provided document is a 510(k) summary for a medical device seeking substantial equivalence to a predicate device. This type of submission often focuses on demonstrating that the new device is as safe and effective as a legally marketed device, rather than performing extensive novel clinical trials as might be seen for entirely new technologies. Therefore, some detailed information about performance comparisons or AI assistance might not be present as it's not typically required for this type of submission.


    Acceptance Criteria and Reported Device Performance

    The document does not explicitly state "acceptance criteria" in a quantitative, measurable format with specific thresholds. Instead, it relies on demonstrating substantial equivalence to a predicate device (Siemens AXIOM Luminos dRF). The performance is discussed in terms of similarities and improvements compared to the predicate, with the underlying assumption that if it's equivalent or better in relevant aspects, it meets necessary performance standards.

    The table below summarizes the comparison:

    Feature / Acceptance Criteria (Implied)Platinum dRF Imaging System (Reported Performance)Siemens AXIOM Luminos dRF (Predicate)Notes / Implicit Acceptance
    Product CodeJAAJAA, OWB, OXOEquivalent primary product code.
    Flat DetectorTrixell Pixium RF 4343 (K080859)Trixell Pixium RF 4343Identical component, implying equivalent image quality at the detector level.
    CollimatorRALCO R225 ACS (K091517)Self manufacturedDifferent manufacturer, but accepted as equivalent.
    Collimator TypeMotorized, remote controlled, with ± 45° manual rotation, automatic lighting, positioning cameraMotorized up to a maximum of ± 45°, detent at 0°Platinum dRF offers more rotational flexibility and features than the predicate.
    Field Coveragemin 4x4 and max 48x48 at 100 cm SIDmin/max not reportedPlatinum dRF provides specific field coverage details.
    Generator Power50-80 kW65 kW or 80 kW (optional)Overlaps with and potentially exceeds predicate's power output.
    AEC Interface4 ionization chambers max (solid state ionization 3 fields)Not availablePlatinum dRF offers an AEC interface not explicitly available on the predicate, an enhancement.
    X-ray tubeVarian 600 kHU tubes RAD92 and G292: 400 kHU tube RAD60Self manufacturedDifferent manufacturer, but accepted as equivalent.
    Use with X-ray ceiling tubeYesYesEquivalent functionality.
    X-ray GridSmit RöntgenSelf manufacturedDifferent manufacturer, but accepted as equivalent.
    Tube motorized rotation+180°/-180°+180°/-90°Platinum dRF offers greater rotational range.
    Oblique projections (Rotational Angle)45°/-45° motorized adjustment, height 10-450mm40°/-40° motorized adjustment, height 10-300mmPlatinum dRF offers slightly larger angle and greater height adjustment range, implying enhanced patient positioning.
    Distance between table-top and detector6.2 cm7 cmSlightly smaller distance for Platinum dRF.
    Anti-diffusion gridOscillating: ratio 10:1, 12:1 / 40 l:cm - 60 l:cm / Multifocus 140 cm, easy ejectionFixed: ratio 15:1, 80 lignes/cm, f0 = 125 cm, easy ejectionDifferent specifications, but implies equivalent or improved anti-diffusion capabilities.
    Movement of the AB selectorMax 158 cm (remotely), increments up to 6 cm/secMax 113 cm (remotely), increments up to 7 cm/sec, PERISTEPPINGPlatinum dRF offers greater remote movement range.
    Compression cone0-160 N with indication above 3 kg5-155 NPlatinum dRF offers a wider compression range, implying broader applicability.
    Imaging SoftwareCMT Thales Duet (K103028)Flurospot COMPACT digital imaging systemDifferent software, but both are standalone cleared/registered components.
    Image Resolution3.4 lp/mm3.4 lp/mmIdentical, demonstrating equivalent image quality. This is a key technical specification for image performance.
    Speed (Radiography)12 f/s (RAD)8 f/s (RAD)Platinum dRF is faster, indicating an improvement.
    Speed (Fluoroscopy)18 f/sec (large field)15 f/sPlatinum dRF is faster, indicating an improvement.
    Dose ReductionYesYesEquivalent functionality.
    DICOMYesYesEquivalent functionality.
    DAP measuring range0.1 - 99,999,999 µGy.m2Not availablePlatinum dRF includes DAP measurement, an enhancement for patient dose management.
    Pulse frequency15, 7.5 and 3 pulsed per sec15, 10, 7.5 and 3 pulsed per secSlightly different options, but within acceptable range for fluoroscopy.
    Table Tilting+90°/-90°, variable tilting up to 10°/sec+90°/-45° or +90°/-90° (optional), two speedsEquivalent or improved tilting.
    Table top height50 cm to 130 cm continuously adjustable50 cm to 100 cm continuously adjustablePlatinum dRF offers a greater adjustable height range, accommodating more patient types.
    Table top dimensions240 x 85 cm / radio transparent field: 283 x 65 cm210 x 80 cm / radio transparent field: 193 x 53.5 cmPlatinum dRF has a larger table top and radio-transparent field, accommodating larger patients.
    Table top attenuation value
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