(144 days)
Not Found
No
The summary describes a standard angiography system with image post-processing and 3D reconstruction capabilities (DynaCT). There is no mention of AI, ML, or any features that would typically indicate the use of such technologies for image analysis, decision support, or automation beyond basic system control and image manipulation. The performance studies described are functional and validation tests, not studies evaluating the performance of an AI/ML algorithm.
No
This device is an angiography system used for diagnostic imaging and image-guided procedures, not for direct therapeutic treatment. While it supports interventional procedures and image-guided surgery, its primary function is visualization and guidance, not the actual therapy.
Yes
The "Intended Use / Indications for Use" section explicitly states that the ARTIS family is developed for "diagnostic imaging" and that the DynaCT software option is "intended for imaging... for diagnosis".
No
The device description clearly states that the ARTIS Family system consists of numerous hardware components including a patient table, C-arm, X-ray tube, flat panel detector, generator, displays, and control modules. While it includes software options like DynaCT, the core device is a complex hardware system.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic) device.
Here's why:
- IVD Definition: In Vitro Diagnostic devices are used to examine specimens taken from the human body (like blood, urine, or tissue) to provide information for diagnosis, monitoring, or screening.
- Device Function: The ARTIS system is an angiography system that uses X-rays to visualize vessels and internal body structures within the patient's body. It is used for imaging, surgical planning, interventional procedures, and treatment follow-up.
- Lack of Specimen Analysis: The description does not mention the analysis of any biological specimens taken from the patient. The imaging is performed directly on the patient.
Therefore, the ARTIS system falls under the category of medical imaging devices, not In Vitro Diagnostic devices.
N/A
Intended Use / Indications for Use
ARTIS is a family of dedicated angiography systems developed for single plane and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
Procedures that can be performed with the ARTIS family include cardiac angiography, neuro-angiography, general angiography, rotational angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures as well as procedures next to the table for i.e. patient extremities. This does not include projection radiography.
Additional procedures that can be performed include angiography in the operating room, image guided surgery by X-ray, by image fusion, and by navigation systems. The examination table as an integrated part of the system can be used for X-ray imaging, surgery and interventions.
The ARTIS systems can also support the acquisition of position triggered imaging for spatial data synthesis.
The ARTIS systems also include the software option DynaCT with following indications for use:
DynaCT is an X-ray imaging software option, which allows the reconstruction of two-dimensional images acquired with a standard angiographic C-arm device into a three-dimensional image format.
DynaCT is intended for imaging both hard and soft tissues as well as other internal body structures for diagnosis, surgical planning, interventional procedures and treatment follow-up.
Product codes
OWB, IZI, JAA, JAK
Device Description
The ARTIS Family (VE40A) system is a medical device that allows visualization of vessels within the human body. It is of the utmost importance to find the right projections so physicians can navigate catheters and other devices safely. The ARTIS Family (VE40A) consists of a patient table and a multi-axis motorized c-arm that can be positioned around the patient and angulated in a double-oblique fashion iso-centering the region of interest between the x-ray tube and the flat panel detector. The X-ray generator is placed separately. The displays for visualizing the X-ray images are mounted at the ceiling with a movable display suspension system. System operation is executed via control modules table side so that the physician can move and position the table and c-arm adequately for best imaging while manipulating catheters or other devices during the x-ray. X-ray release is tableside via a footswitch.
The ARTIS Family (VE40A) modular angiography systems are designed as sets of components that may be combined into four different confiqurations (Biplane, Floor, Ceiling, or the ARTIS pheno) to provide specialized angiography systems. In general, they are equipped with a C-arm, stand, flat panel detector, x-ray tube, collimator, high voltage generator, patient table, and image post-processing.
The ARTIS Family (VE40A) covers the complete range of angiographic applications, cardiac angiography, neuro-angiography, general angiography, surgery and surgical angiography, multipurpose angiography, rotational angiography, and radiographic/fluoroscopic procedures.
The following components are configured to create a Floor or Biplane configuration:
- (1) Floor stand with C-arm, X-ray tube assembly, and FD
- (2) Patient table
- (3) Display ceiling suspension with displays
- (4) Footswitch for releasing radiation
- (5) Control console for controlling the stand, patient table, and imaging system
Images and operating elements are displayed on screens. Depending on the ARTIS Family (VE40A) system configurations, different display variants are used to visualize image and information content. Displays that visualize single images or large displays that are configurable to visualize multiple images and information contained in various layouts are used.
Post-processing can be done in the exam room or in the control room that offers monitors as well, with a footswitch location in the exam room or the control room. The ARTIS Family (VE40A) Systems are capable of 2D and 3D imaging. The c-arms can be mounted on the floor or for biplane systems on the floor, the ceiling or ARTIS pheno. Other systems and software syngo Application Software, syngo X Workplace, Sensis, and or third-party systems may also be integrated into the ARTIS Family (VE40A) screen configuration.
Different screen configurations and layouts are possible examination and control rooms.
The Subject device ARTIS Family (VE40A) supports the following modifications.
Software / Hardware changes specific to ARTIS Family (VE40A)
- Updated system software from VE30A to VE40A (ARTIS icono floor & Biplane; & ARTIS pheno)
A. Added an optional Display - Updated system software from VE23 to VE40A (ARTIS icono ceiling)
A. Added feature "Xpand" (lateral movement of ceiling stand, ARTIS icono ceiling only) - Added an optional Display
- Added new PC for imaging System due to obsolescence
Mentions image processing
Yes
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
X-Ray
Anatomical Site
Not Found
Indicated Patient Age Range
pediatric and obese patients
Intended User / Care Setting
Not Found
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Nonclinical Performance Testing:
During product development, non-clinical tests were conducted for the ARTIS Family (VE40A). The following non-clinical testing was conducted on the presented modifications: XPAND - Ceiling Transversal Flow testing the steps the user performed to move the C-arm of the ARTIS icono ceiling system to several positions such as transfer positions, radial access position, typical cardiology projection. Software functional, verification, and System validation testing were conducted with passing results.
The ARTIS Family (VE40A) was certified by Siemens Healthcare GmbH Corporate Testing Laboratory to comply with several standards for Electrical safety, performance and Electromagnetic Compatibility.
The modifications described in this Premarket Notification are supported with verification and validation testing.
Software Documentation for a Basic documentation level per FDA's Guidance Document "Guidance for the Content of Premarket Submissions for "Guidance for the Content of Premarket Submissions for Device Software Functions" issued on June 14, 2023, and "Off-The-Shelf Software Use in Medical Devices" was conducted. The performance data demonstrates continued conformance with medical devices containing software. During product development, non-clinical tests were conducted on ARTIS Family System software (VE40A).
The Risk analysis was completed, and risk control was implemented to mitigate identified hazards. The testing results show that all the software specifications have met the acceptance criteria. Testing for verification of the device was found acceptable to support the claims of substantial equivalence.
ARTIS Family Systems software (VE40A) was tested and found to be substantially equivalent for intended users, uses, and use environments through the design control verification and validation process.
Summary:
Performance tests were conducted to evaluate the functionality of the ARTIS Family (VE40A) Systems. These tests have been performed to assess the functionality of the subject device. The results of all conducted testing were found acceptable and did not raise any new issues of safety or effectiveness.
Conclusion as to Substantial Equivalence:
The predicate devices were cleared based on non-clinical supportive information. Non-clinical test results demonstrate that the ARTIS Family (VE40A) acceptance criteria are adequate for the intended use of the device. The comparison of technological characteristics, non-clinical performance data, and software validation data demonstrates that the Subject Device is as safe and effective when compared to the Predicate Devices that are currently marketed for the same intended use.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 892.1650 Image-intensified fluoroscopic x-ray system.
(a)
Identification. An image-intensified fluoroscopic x-ray system is a device intended to visualize anatomical structures by converting a pattern of x-radiation into a visible image through electronic amplification. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.(b)
Classification. Class II (special controls). An anthrogram tray or radiology dental tray intended for use with an image-intensified fluoroscopic x-ray system only is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 892.9. In addition, when intended as an accessory to the device described in paragraph (a) of this section, the fluoroscopic compression device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 892.9.
0
October 22, 2024
Image /page/0/Picture/1 description: The image shows the logo of the U.S. Food and Drug Administration (FDA). The logo consists of two parts: the Department of Health & Human Services logo on the left and the FDA logo on the right. The FDA logo features the letters "FDA" in a blue square, followed by the words "U.S. FOOD & DRUG ADMINISTRATION" in blue text.
Siemens Medical Solutions USA, Inc % Patricia Jones Regulatory Affairs Professional 40 Liberty Boulevard MALVERN, PA 19355
Re: K241572
Trade/Device Name: ARTIS icono (VE40A) (floor); ARTIS icono (VE40A) (biplane); ARTIS icono (VE40A) (ceiling); ARTIS pheno (VE40A) Regulation Number: 21 CFR 892.1650 Regulation Name: Image-Intensified Fluoroscopic X-Ray System Regulatory Class: Class II Product Code: OWB, IZI, JAA, JAK Dated: May 31, 2024 Received: May 31, 2024
Dear Patricia Jones:
We have reviewed your section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (the Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database available at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
1
Additional information about changes that may require a new premarket notification are provided in the FDA guidance documents entitled "Deciding When to Submit a 510(k) for a Change to an Existing Device" (https://www.fda.gov/media/99812/download) and "Deciding When to Submit a 510(k) for a Software Change to an Existing Device" (https://www.fda.gov/media/99785/download).
Your device is also subject to, among other requirements, the Quality System (QS) regulation (21 CFR Part 820), which includes, but is not limited to, 21 CFR 820.30. Design controls; 21 CFR 820.90. Nonconforming product; and 21 CFR 820.100, Corrective and preventive action. Please note that regardless of whether a change requires premarket review, the QS regulation requires device manufacturers to review and approve changes to device design and production (21 CFR 820.30 and 21 CFR 820.70) and document changes and approvals in the device master record (21 CFR 820.181).
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR Part 803) for devices or postmarketing safety reporting (21 CFR Part 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR Part 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR Parts 1000-1050.
All medical devices, including Class I and unclassified devices and combination product device constituent parts are required to be in compliance with the final Unique Device Identification System rule ("UDI Rule"). The UDI Rule requires, among other things, that a device bear a unique device identifier (UDI) on its label and package (21 CFR 801.20(a)) unless an exception or alternative applies (21 CFR 801.20(b)) and that the dates on the device label be formatted in accordance with 21 CFR 801.18. The UDI Rule (21 CFR 830.300(a) and 830.320(b)) also requires that certain information be submitted to the Global Unique Device Identification Database (GUDID) (21 CFR Part 830 Subpart E). For additional information on these requirements, please see the UDI System webpage at https://www.fda.gov/medical-device-advicecomprehensive-regulatory-assistance/unique-device-identification-system-udi-system.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.
For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatory
2
assistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely,
Lu Jiang
Lu Jiang, Ph.D. Assistant Director Diagnostic X-ray Systems Team DHT8B: Division of Radiologic Imaging Devices and Electronic Products OHT8: Office of Radiological Health Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
3
Indications for Use
Submission Number (if known)
Device Name
ARTIS icono (VE40A) (floor); ARTIS icono (VE40A) (biplane); ARTIS icono (VE40A) (ceiling); ARTIS pheno (VE40A)
Indications for Use (Describe)
ARTIS is a family of dedicated angiography systems developed for single plane and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
Procedures that can be performed with the ARTIS family include cardiac angiography, neuroanqiography, general angiography, rotational angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures as well as procedures next to the table for i.e. patient extremities. This does not include projection radiography.
Additional procedures that can be performed include angiography in the operating room, image guided surgery by X-ray, by image fusion, and by navigation systems. The examination table as an integrated part of the system can be used for X-ray imaging, surgery and interventions.
The ARTIS systems can also support the acquisition of position triggered imaging for spatial data synthesis.
The ARTIS systems include also the software option DynaCT with following indications for use:
DynaCT is an X-ray imaging software option, which allows the reconstruction of two-dimensional images acquired with a standard angiographic C-arm device into a three-dimensional image format.
DynaCT is intended for imaging both hard and soft tissues as well as other internal body structures for diagnosis, surgical planning, interventional procedures and treatment follow-up.
Type of Use (Select one or both, as applicable)
Prescription Use (Part 21 CFR 801 Subpart D)
over-The-Counter Use (21 CFR 801 Subpart C)
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Image /page/4/Picture/0 description: The image shows the Siemens Healthineers logo. The word "SIEMENS" is in teal, and the word "Healthineers" is in orange. To the right of the word "Healthineers" is a graphic of orange dots.
510(k) Summary: ARTIS icono (VE40A) (floor) ARTIS icono (VE40A) (biplane) ARTIS icono (VE40A) (ceiling) ARTIS pheno (VE40A)
510(k) Number: K241572
Siemens Medical Solutions USA, Inc. Company: 40 Liberty Boulevard, 65 Malvern, PA 19355
Date Prepared: October 22, 2024
1. General Information: Importer / Distributor: Siemens Medical Systems USA, Inc. 40 Liberty Boulevard, 65-1A Malvern, PA 19355 Establishment Registration Number: 2240869
Manufacturing Site:
Siemens Healthineers AG Siemensstr. 1 91301 Forchheim, Germany Establishment Registration Number: 3004977335
2. Contact Person:
Ms. Patricia D. Jones Regulatory Affairs Professional Siemens Medical Solutions USA, Inc. 40 Liberty Boulevard Malvern, PA 19355 Phone: (678) 575-8832 Email: patricia.jones@siemens-Healthineers.com
3. Device Name and Classification: Trade Name:
| Trade Name: | ARTIS icono (VE40A) (floor)
ARTIS icono (VE40A) (biplane)
ARTIS icono (VE40A) (ceiling)
ARTIS pheno (VE40A) |
|-----------------------|----------------------------------------------------------------------------------------------------------------------|
| Classification Name: | Image-intensified fluoroscopic X-ray System |
| Common Name: | Interventional Fluoroscopic X-Ray System |
| Classification Panel: | Radiology |
| Regulation Number: | 21 CFR §892.1650 |
| Device Class: | Class II |
| Primary Product Code: | OWB |
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Image /page/5/Picture/0 description: The image shows the logo for Siemens Healthineers. The word "SIEMENS" is in teal, and the word "Healthineers" is in orange. To the right of the word "Healthineers" is a cluster of orange dots.
Subsequent Product Codes:
IZI, JAA, JAK
4. Legally Marketed Primary Predicate Device
Trade Name: 510(k) Clearance Clearance Date Classification Name: Common Name: Classification Panel: Regulation Number: Device Class: Primary Product Code: Subsequent Product Codes: Total Product Life Cycle:
ARTIS icono (VE30A) K230950 December 14, 2023 Image-intensified fluoroscopic X-ray System Interventional Fluoroscopic X-ray System Radiology 21 CFR §892.1650 Class II OWB IZI, JAA, JAK All product Recall incidents are considered during the Design Input phase of development to ensure the latest models will not be affected by any of the
Secondary Predicate Device Trade Name: 510(k) Clearance Clearance Date Classification Name: Common Name: Classification Panel: Regulation Number: Device Class: Primary Product Code: Subsequent Product Codes: Total Product Life Cycle:
Secondary Predicate Device Trade Name: 510(k) Clearance Clearance Date Classification Name: Common Name: Classification Panel: Regulation Number: Device Class: Primary Product Code: Subsequent Product Codes:
ARTIS icono (VE23) System
applicable issues.
K221516 July 19, 2022 Image-intensified fluoroscopic X-ray System Interventional Fluoroscopic X-ray System Radiology 21 CFR 8892.1650 Class II OWB IZI. JAA. JAK All product Recall incidents are considered during the
Design Input phase of development to ensure the latest models will not be affected by any of the applicable issues.
ARTIS pheno (VE30A)
K230949 December 15, 2023 Image-intensified fluoroscopic X-ray System Interventional Fluoroscopic X-ray System Radiology 21 CFR §892.1650 Class II OWB JAA
6
Total Product Life Cycle:
All product Recall incidents are considered du n Input phase of development to ensure the latest models will not be affected by any of the applicable issues.
5. Device Description:
The ARTIS Family (VE40A) system is a medical device that allows visualization of vessels within the human body. It is of the utmost importance to find the right projections so physicians can navigate catheters and other devices safely. The ARTIS Family (VE40A) consists of a patient table and a multi-axis motorized c-arm that can be positioned around the patient and angulated in a double-oblique fashion iso-centering the region of interest between the x-ray tube and the flat panel detector. The X-ray generator is placed separately. The displays for visualizing the X-ray images are mounted at the ceiling with a movable display suspension system. System operation is executed via control modules table side so that the physician can move and position the table and c-arm adequately for best imaging while manipulating catheters or other devices during the x-ray. X-ray release is tableside via a footswitch.
The ARTIS Family (VE40A) modular angiography systems are designed as sets of components that may be combined into four different confiqurations (Biplane, Floor, Ceiling, or the ARTIS pheno) to provide specialized angiography systems. In general, they are equipped with a C-arm, stand, flat panel detector, x-ray tube, collimator, high voltage generator, patient table, and image post-processing.
The ARTIS Family (VE40A) covers the complete range of angiographic applications, cardiac angiography, neuro-angiography, general angiography, surgery and surgical angiography, multipurpose angiography, rotational angiography, and radiographic/fluoroscopic procedures.
The following components are configured to create a Floor or Biplane configuration:
- (1) Floor stand with C-arm, X-ray tube assembly, and FD
- (2) Patient table
- (3) Display ceiling suspension with displays
- (4) Footswitch for releasing radiation
- (5) Control console for controlling the stand, patient table, and imaging system
Images and operating elements are displayed on screens. Depending on the ARTIS Family (VE40A) system configurations, different display variants are used to visualize image and information content. Displays that visualize single images or large displays that are configurable to visualize multiple images and information contained in various layouts are used.
Post-processing can be done in the exam room or in the control room that offers monitors as well, with a footswitch location in the exam room or the control room. The ARTIS Family (VE40A) Systems are capable of 2D and 3D imaging. The c-arms can be mounted on the floor or for biplane systems on the floor, the ceiling or ARTIS pheno. Other systems and software syngo Application Software, syngo X Workplace, Sensis, and or third-party systems may also be integrated into the ARTIS Family (VE40A) screen configuration.
7
Different screen configurations and layouts are possible examination and control rooms.
The Subject device ARTIS Family (VE40A) supports the following modifications.
| Software / Hardware changes specific to ARTIS Family (VE40A) |
|---|
| 1. Updated system software from VE30A to VE40A (ARTIS icono floor & Biplane; & ARTIS pheno) |
| A. Added an optional Display |
| 2. Updated system software from VE23 to VE40A (ARTIS icono ceiling) |
| A. Added feature "Xpand" (lateral movement of ceiling stand, ARTIS icono ceiling only) |
| 3. Added an optional Display |
| 4. Added new PC for imaging System due to obsolescence |
6. Indications for Use:
ARTIS is a family of dedicated angiography systems developed for single-plane and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
Procedures that can be performed with the ARTIS family include cardiac angiography, neuro-angiography, general angiography, rotational angiography, multipurpose angiography, and whole body radiographic/fluoroscopic procedures as well as procedures next to the table for i.e., patient extremities. This does not include projection radiography.
Additional procedures that can be performed include angiography in the operating room, image guided surgery by X-ray, by image fusion, and by navigation systems. The examination table as an integrated part of the system can be used for X-ray imaging, surgery and interventions.
The ARTIS systems can also support the acquisition of position-triggered imaging for spatial data svnthesis.
The ARTIS systems also include the software option DynaCT with following indications for use:
DynaCT is an X-ray imaging software option, which allows the reconstruction of twodimensional images acquired with a standard angiographic C-arm device into a threedimensional image format.
DynaCT is intended for imaging both hard and soft tissues as well as other internal body structures for diagnosis, surgical planning, interventional procedures and treatment followup.
7. Substantial Equivalence:
The ARTIS Family (VE40A) of systems is substantially equivalent to the legally marketed predicate listed in the table below:
n the
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Image /page/8/Picture/0 description: The image contains the logo for Siemens Healthineers. The word "SIEMENS" is written in teal, and the word "Healthineers" is written in orange below it. To the right of the words is a graphic of orange dots arranged in a circular pattern.
| Predicate Device Name and
Manufacturer | 510(k)
Number | Clearance
Date | Comparable Properties |
|-----------------------------------------------------------------------------------------|------------------|-------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Primary Predicate Device:
ARTIS icono (VE30A)
(Floor & Biplane)
Siemens | K230950 | 12/14/2023 | Indications for Use Statement Updated system software from VE23 to VE40A Added an optional Display |
| Secondary Predicate Device:
ARTIS icono (VE23)
(Ceiling Configuration)
Siemens | K221516 | 07/19/2022 | Indications for Use Statement Updated system software from VE23 to VE40A Added feature "Xpand" (lateral movement of ceiling stand, ARTIS icono ceiling only) Added optional Display Added new PC |
| Secondary Predicate Device:
ARTIS pheno (VE30A)
Siemens | K230949 | 12/15/2023 | Added an optional Display |
Table 3: Predicate Device Comparable Properties for Subject Device Modifications:
8. Summary of Technological Characteristics of the Subject Device as Compared with the Predicate Device:
The ARTIS Family (VE40A) System is designed as a set of components (C-arm, X-ray tube, and housing, flat panel detector, digital imaging system, collimator, generator etc.) that may be combined into four different configurations (Floor, Biplane, ceiling or the ARTIS pheno to provide specialized angiography systems. Components used with ARTIS configurations are either commercially available with current Siemens systems or included modifications to existing components. Technological differences between the Subject Device and the Predicate Device are provided in Table 4 below for all modifications.
9
| SIEMENS .: |
|---|
| . | |
|---|---|
| . | |
| A LA LALA | |
| Modifications | Subject Device
ARTIS icono (VE40A) (floor)
ARTIS icono (VE40A) (biplane)
ARTIS icono (VE40A) (ceiling)
ARTIS pheno (VE40A) | Primary Predicate Device
ARTIS icono (VE30A)
K230950
Secondary Predicate Device
ARTIS pheno (VE30A)
K230949 | Comparison
Results |
|------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| New System
Software/
Hardware
Changes | 1. Updated system software from VE30A to
VE40A (ARTIS icono floor & Biplane; & ARTIS
pheno)
A. Added an optional Display | System software version VE30A | Comparable:
System software VE30 was updated to support
modifications 1A & 2A, 3 & 4. All Software
modifications conform to "Guidance for the
Content of Premarket Submissions for Device
Software Functions." |
| | 2. Updated system software from VE23 to VE40A
(ARTIS icono ceiling) | Displays
Secondary Predicate Device
ARTIS icono (VE23)
K221516 | |
| | A. Added feature "Xpand" (lateral movement
of ceiling stand, ARTIS icono ceiling only) | System software version VE23A
(Ceiling configuration)
Ceiling Longitudinal movement
only | Bench tests were conducted and found
acceptable and did not raise any new safety or
effectiveness issues. |
| | 3. Added an optional Display
4. Added new PC for imaging System due to
obsolescence | Displays
PC | All software validation data demonstrates that
the Subject device is as safe and effective as
the Predicate Device currently marketed for the
same intended use. All test results met all
acceptance criteria. |
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Image /page/10/Picture/0 description: The image shows the logo for Siemens Healthineers. The word "SIEMENS" is in teal, and the word "Healthineers" is in orange. To the right of the word "Healthineers" is a graphic of orange dots arranged in a circular pattern.
9. Nonclinical Performance Testing:
During product development, non-clinical tests were conducted for the ARTIS Family (VE40A). The following non-clinical testing was conducted on the presented modifications: XPAND - Ceiling Transversal Flow testing the steps the user performed to move the C-arm of the ARTIS icono ceiling system to several positions such as transfer positions, radial access position, typical cardiology projection. Software functional, verification, and System validation testing were conducted with passing results.
The ARTIS Family (VE40A) was certified by Siemens Healthcare GmbH Corporate Testing Laboratory to comply with the following standards for Electrical safety, performance and Electromagnetic Compatibility:
| Recog-
nition # | Product Area | Title of Standard | Reference
Number and Date | Standards
Development
Organization |
|--------------------|-------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------|------------------------------------------|
| 19-46 | General II (ES/
EMC) | Medical electrical equipment -
Part 1: General requirements for
basic safety and essential
performance (IEC 60601-
1:2005, MOD) [Including
Amendment 2 (2021)] | ES60601-
1:2005/(R)2012 &
A1:2012,
C1:2009/(R)2012
&
A2:2010/(R)2012
(Cons. Text) [Incl.
AMD2:2021] | ANSI AAMI |
| 19-36 | General II
(ES/EMC) | Medical Electrical Equipment:
Part 1: 1. Collateral Standard:
Electromagnetic compatibility –
Requirements and tests | 60601-1-2:2020 | IEC |
| 12-336 | Radiology | Medical electrical equipment -
Part 1-3: General requirements
for basic safety and essential
performance - Collateral
Standard: Radiation protection
in diagnostic X-ray equipment | 60601-1-3:2021 | IEC |
| 12-273 | Radiology | Safety of laser products - Part 1:
Equipment classification and
Requirements | 60825-1:2014
(recognized 2007) | IEC |
| 5-137 | General I
(QS/RM) | Graphical symbols for electrical
equipment in medical practice | TR 60878:2022 | IEC |
| 13-79 | Software/
Informatics | Medical Device Software –
Software Life Cycle Processes | 62304:2015 | IEC |
| 12-309 | Radiology | Medical electrical equipment -
Part 2-28: Particular
requirements for basic safety
and essential performance of X-
ray tube assemblies for medical
diagnosis | 60601-2-28:2017 | IEC |
| 12-351 | Radiology | Medical electrical equipment -
Part 2-43: Particular
requirements for the safety and | 60601-2-43:2022 | IEC |
| Recog-
nition # | Product Area | Title of Standard | Reference
Number and Date | Standards
Development
Organization |
| | | essential performance of X-ray
equipment for interventional
procedures | | |
| 12-348 | Radiology | Medical electrical equipment -
Part 2-54: Particular
requirements for the basic
safety and essential
performance of X-ray equipment
for radiography and radioscopy | 60601-2-54:2022 | IEC |
| 2-258 | Biocompatibility | Biological evaluation of medical
devices - Part 1: Evaluation and
testing within a risk
management process | 10993-1:2018 | ISO |
| 5-125 | General I
(QS/RM) | Medical devices: Application of
Risk management to medical
devices | 14971:2019 | ISO |
| 5-134 | General I
(QS/RM) | Medical devices - Symbols to be
used with information to be
supplied by the manufacturer -
Part 1: General requirements | 15223-1:2021 | ISO |
| 14-579 | Sterility | Processing of health care
products - Information to be
provided by the medical device
manufacturer for the processing
of medical devices - Part 2:
Non-critical medical devices. | 17664-2:2021 | ISO |
| 6-483 | General Plastic
Surgery/
General Hospital | Medical electrical equipment -
Part 2-35: Particular
requirements for the basic
safety and essential
performance of heating devices
using blankets, pads and
mattresses and intended for
heating in medical use | 60601-2-35:2020 | IEC |
| 5-129 | General I
(QS/RM) | Medical devices - Part 1:
Application of usability
engineering to medical devices | 62366-1:2020 | IEC |
| 12-341 | Radiology | Medical electrical equipment -
Medical image display systems -
Part 1: Evaluation methods | 62563-1:2021 | IEC |
| 12-344 | Radiology | Medical electrical equipment -
Medical image display systems -
Part 2: Acceptance and
constancy tests for medical
image displays | 62563-2:2021 | IEC |
| 12-349 | Radiology | Digital Imaging and
Communications in Medicine
(DICOM) Set | PS 3.1:2022 | NEMA |
| Recog-
nition # | Product Area | Title of Standard | Reference
Number and Date | Standards
Development
Organization |
| 13-96 | Software/
Informatics | Standard for Safety, Standard
for Software Cybersecurity
Network-Connectable Products,
Part 1: General Requirements | 2900-1:2017 | ANSI UL |
| 13-104 | Software/
Informatics | Standard for Safety, Software
Cybersecurity for Network-
Connectable Products, Part 2-1:
Particular Requirements for
Network Connectable
Components of Healthcare and
Wellness Systems | 2900-2-1:2017 | ANSI UL |
| 13-83 | Software/
Informatics | Principles for medical device
security - Risk management. | TIR57:2016 | AAMI |
| 5-132 | General I (QS/
RM) | Medical electrical equipment -
Part 1-6: General requirements
for basic safety and essential
performance - Collateral
standard: Usability | 60601-1-6:2020 | IEC |
| 19-22 | General II (ES/
EMC) | Technical Information Report
Risk management of radio-
frequency wireless coexistence
for medical devices and
systems. | TIR69:2017/
(R2020) | AAMI |
| 19-48 | General II (ES/
EMC) | American National Standard for
Evaluation of Wireless
Coexistence | USEMCSC
C63.27-2021 | IEEE ANSI |
| 19-19 | General II (ES/
EMC) | Medical electrical equipment -
Part 4-2: Guidance and
interpretation - Electromagnetic
immunity: performance of
medical electrical equipment
and medical electrical systems | TR 60601-4-
2:2016 | IEC |
| 5-135 | General I (QS/
RM) | Medical devices - Information to
be supplied by the manufacturer | 20417:2021 | ISO |
11
Image /page/11/Picture/0 description: The image shows the Siemens Healthineers logo. The word "SIEMENS" is in teal, and the word "Healthineers" is in orange. To the right of the words is a graphic of orange dots arranged in a circular pattern.
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Image /page/12/Picture/0 description: The image contains the logo for Siemens Healthineers. The word "SIEMENS" is written in teal, and the word "Healthineers" is written in orange below it. To the right of the words is a graphic of orange dots arranged in a circular pattern.
The modifications described in this Premarket Notification are supported with verification and validation testing.
Verification and Validation:
Software Documentation for a Basic documentation level per FDA's Guidance Document "Guidance for the Content of Premarket Submissions for "Guidance for the Content of Premarket Submissions for Device Software Functions" issued on June 14, 2023, and "Off-The-Shelf Software Use in Medical Devices" was conducted. The performance data demonstrates continued conformance with medical devices containing software. During product development, non-clinical tests were conducted on ARTIS Family System software (VE40A).
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Image /page/13/Picture/0 description: The image shows the Siemens Healthineers logo. The word "SIEMENS" is in teal, and the word "Healthineers" is in orange. To the right of the words is a graphic of orange dots arranged in a circular pattern.
The Risk analysis was completed, and risk control was implemented to mitigate identified hazards. The testing results show that all the software specifications have met the acceptance criteria. Testing for verification of the device was found acceptable to support the claims of substantial equivalence.
ARTIS Family Systems software (VE40A) was tested and found to be substantially equivalent for intended users, uses, and use environments through the design control verification and validation process. Customer employees are adequately trained in the use of this equipment.
Siemens conforms to the cybersecurity requirementing a process of preventing unauthorized access, modifications, misuse, or denial of use, or the unauthorized use of information that is stored, accessed, or transferred from a medical device to an external recipient. The responsibility for compliance with IEC 80001-1-2010 is the hospital.
Summary:
Performance tests were conducted to evaluate the functionality of the ARTIS Family (VE40A) Systems. These tests have been performed to assess the functionality of the subject device. The results of all conducted testing were found acceptable and did not raise any new issues of safety or effectiveness.
10. General Concerns:
Instructions for use are included within the device labeling, and the information provided will enable the user to operate the device safely and effectively.
Risk management is ensured via a hazard analysis, which is used to identify potential hazards. These potential hazards are controlled via software development, verification, and validation testing. To minimize electrical, and radiation hazards. Siemens adheres to recognized and established industry practices, and all equipment is subject to final performance testing. Furthermore, the operators are healthcare professionals who are trained and responsible for evaluating the postprocessing of X-ray images.
11. Conclusion as to Substantial Equivalence:
The predicate devices were cleared based on non-clinical supportive information. Non-clinical test results demonstrate that the ARTIS Family (VE40A) acceptance criteria are adequate for the intended use of the device. The comparison of technological characteristics, non-clinical performance data, and software validation data demonstrates that the Subject Device is as safe and effective when compared to the Predicate Devices that are currently marketed for the same intended use.