Who is the manufacturer of syngo.via View&GO VA40A?

Siemens Healthcare GmbH filed the 510(k) submission for syngo.via View&GO VA40A (K230196).

What is the FDA product code for syngo.via View&GO VA40A?

LLZ. It is classified under 21 CFR 892.2050 as a Class 2 device in the Radiology panel.

What is the regulatory pathway for syngo.via View&GO VA40A?

510(k) clearance (submission type: Traditional).

What are the predicate devices for syngo.via View&GO VA40A?

syngo.via View&GO (Version VA30A) (K221501).

Who can help prepare an FDA 510(k) submission like syngo.via View&GO VA40A?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

syngo.via View&GO VA40A

K230196 · Siemens Healthcare GmbH · LLZ · Feb 13, 2023 · Radiology

Device Facts

Record ID	K230196
Device Name	syngo.via View&GO VA40A
Applicant	Siemens Healthcare GmbH
Product Code	LLZ · Radiology
Decision Date	Feb 13, 2023
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 892.2050
Device Class	Class 2
Attributes	Software as a Medical Device, 3rd-Party Reviewed

Indications for Use

syngo.via View&GO is a software solution intended to be used for viewing, manipulation, communication, and storage of medical images. It can be used as a stand-alone device or together with a variety of cleared and unmodified syngo based software options. syngo.via View&GO supports interpretation and evaluation of examinations within healthcare institutions, for example, in Radiology, Nuclear Medicine and Cardiology environments. The system is not intended for the displaying of digital mammography images for diagnosis in the U.S.

Device Story

Software-only medical device (VA40A) for viewing, post-processing, and communication of DICOM images; installed on standard IT hardware. Used in radiology, nuclear medicine, and cardiology departments by clinicians. Inputs include DICOM images from various modalities (CT, MR, NM, XA, US, DX). Performs image rendering (MPR, MIP/MinIP, VRT, SSD, Cinematic VRT), registration, and measurements. Outputs displayed on monitors for clinical review. Supports clinical decision-making by providing visualization tools; not intended as sole diagnostic basis. Features include series navigation, spine/rib labeling, and data export. Cybersecurity controls include user access, audit trails, and firewall support.

Clinical Evidence

Bench testing only. No clinical data provided. Verification and validation testing confirmed software specifications met acceptance criteria and demonstrated substantial equivalence.

Technological Characteristics

Software-only PACS/image processing system; runs on Microsoft Windows 10/11. Supports DICOM networking (TCP/IP). Features include MPR, VRT, Cinematic VRT, and automated spine/rib labeling. Cybersecurity includes user access control, audit trails, and malware protection. Conforms to NEMA PS 3.1-3.20, ISO 14971, IEC 62304, IEC 62366-1, and IEEE Std 3333.2.1-2015.

Indications for Use

Indicated for image rendering and post-processing of DICOM images to support interpretation in radiology, nuclear medicine, and cardiology. Not indicated for diagnostic mammography in the U.S. Not for use as a patient image archiving device or as the sole basis for clinical decisions.

Regulatory Classification

Identification

A medical image management and processing system is a device that provides one or more capabilities relating to the review and digital processing of medical images for the purposes of interpretation by a trained practitioner of disease detection, diagnosis, or patient management. The software components may provide advanced or complex image processing functions for image manipulation, enhancement, or quantification that are intended for use in the interpretation and analysis of medical images. Advanced image manipulation functions may include image segmentation, multimodality image registration, or 3D visualization. Complex quantitative functions may include semi-automated measurements or time-series measurements.

Special Controls

*Classification.* Class II (special controls; voluntary standards—Digital Imaging and Communications in Medicine (DICOM) Std., Joint Photographic Experts Group (JPEG) Std., Society of Motion Picture and Television Engineers (SMPTE) Test Pattern).

Predicate Devices

syngo.via View&GO (Version VA30A) (K221501)

Reference Devices

Syngo Carbon Space VA20A (K213665)

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image contains two logos. On the left is the Department of Health & Human Services logo. On the right is the FDA logo, which includes the letters "FDA" in a blue square, followed by the words "U.S. FOOD & DRUG ADMINISTRATION" in blue text. Siemens Healthcare GmBH % Prithul Bom Most Responsible Person Regulatory Technology Services, LLC 1000 Westgate Drive, Suite 510k SAINT PAUL MN 55114 #### Re: K230196 February 13, 2023 Trade/Device Name: syngo.via View&GO VA40A Regulation Number: 21 CFR 892.2050 Regulation Name: Medical image management and processing system Regulatory Class: Class II Product Code: LLZ Dated: January 24, 2023 Received: January 25, 2023 Dear Prithul Bom: 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 (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 located 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. 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 {1}------------------------------------------------ 801); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 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 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 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 mediation-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-regulatoryassistance/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. Jessica Lamb Jessica Lamb, Ph.D. Assistant Director Imaging Software Team DHT8B: Division of Radiological Imaging Devices and Electronic Products OHT8: Office of Radiological Health Office of Product Evaluation and Quality Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ # Indications for Use 510(k) Number (if known) K230196 Device Name syngo.via View&GO VA40A #### Indications for Use (Describe) Indications for Use syngo.via View&GO is indicated for image rendering and post-processing of DICOM images to support the interpretation in the field of radiology, nuclear medicine and cardiology. #### Contraindications The system is not indicated for mammography images for diagnosis in the U.S. The application is not to be used as an archiving device for patients' image data. The application is not to be used as a sole basis for clinical decisions but further evidence has to be taken into account. | Type of Use (Select one or both, as applicable) | | |-------------------------------------------------|--| |-------------------------------------------------|--| X Prescription Use (Part 21 CFR 801 Subpart D) Over-The-Counter Use (21 CFR 801 Subpart C) #### CONTINUE ON A SEPARATE PAGE IF NEEDED. This section applies only to requirements of the Paperwork Reduction Act of 1995. #### *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.* The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: > Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff(@fda.hhs.gov "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." {3}------------------------------------------------ Section E: 510(k) Summary {4}------------------------------------------------ # 510(k) Summary This summary of 510(k) safety and effectiveness information is being submitted in accordance with the requirements of SMDA 1990 and 21 CFR §807.92. Date prepared: January 10, 2023 - 1. Submitter: Siemens Healthcare GmbH Henkestrasse 127 91052 Erlangen Germany Establishment Registration Number: 3004977335 #### 2. Contact Person: Ms. Frederike Jakob Regulatory Affairs Manager Siemens Healthcare GmbH, Siemensstr. 1 91301 Forchheim Germany E-mail: Frederike.Jakob(@siemens-healthineers.com Telephone: +49 (0)162 109 2694 Fax: +49 (9191) 18-4404 #### 3. Device Name and Classification: | Trade Name: | syngo.via View&GO (Version VA40A) | |-----------------------|-------------------------------------------------------| | Classification Name: | Medical Image Management and Processing System (PACS) | | Classification Panel: | Radiology | | CFR Section: | 21 CFR §892.2050 | | Device Class: | Class II | | Product Code: | LLZ | #### 4. Legally Marketed Predicate Device: | Trade Name: | syngo.via View&GO (Version VA30A) | |-----------------------|----------------------------------------------------------------------------------| | 510(k) Clearance: | K221501 | | Clearance Date: | October 14, 2022 | | Classification Name: | Medical Image Management and Processing System (PACS) | | Classification Panel: | Radiology | | CFR Section: | 21 CFR §892.2050 | | Device Class: | Class II | | Product Code: | LLZ | | Recall Information: | This predicate device has not been the subject of any design related recalls. | {5}------------------------------------------------ - 5. Additional Legally Marketed Reference Device | Trade Name: | Syngo Carbon Space VA20A | |-----------------------|------------------------------------------------------------------------| | 510(k) Clearance: | K213665 | | Clearance Date: | June 21, 2022 | | Classification Name: | Medical Image Management and Processing System | | Classification Panel: | Radiology | | CFR Section: | 21 CFR §892.2050 | | Device Class: | Class II | | Product Code: | LLZ | | Recall Information: | This device has not been the subject of any design related recalls. | #### Device Description: Siemens Healthcare GmbH intends to market the Medical Image Management and Processing System, syngo.via View&GO, software version VA40A. This 510(k) submission describes several modifications to the previously cleared predicate device. syngo.via View&GO, software version VA30A. syngo.via View&GO is a software-only medical device, which is delivered by download to be installed on common IT hardware. This hardware has to fulfil the defined requirements. Any hardware platform that complies to the specified minimum hardware and software requirements and with successful installation verification and validation activities can be supported. The hardware itself is not seen as part of the medical device syngo.via View&GO and therefore not in the scope of this 510(k) submission. syngo.via View&GO provides tools and features to cover the radiological tasks preparation for reading, reading images and support reporting. syngo.via View&GO supports DICOM formatted images and objects. syngo.via View&GO is a standalone viewing and reading workplace. This is capable of rendering the data from the connected modalities for the post processing activities. syngo.via View&GO provides the user interface for interactive image viewing and processing with a limited short-term storage which can be interfaced with any Long-term storage (e.g. PACS) via DICOM syngo.via View&GO is based on Microsoft Windows operating systems. syngo.via View&GO supports various monitor setups and can be adapted to a range of image types by connecting different monitor types. The subject device and the predicate device share fundamental scientific technology. This device description holds true for the subject device. syngo.via View&GO, software version VA40A, as well as the predicate device, syngo.via View&GO, software version VA30A. {6}------------------------------------------------ ## 6. Intended Purpose: ## 6.1 Intended Use syngo.via View&GO is a software solution intended to be used for viewing, manipulation, communication, and storage of medical images. It can be used as a stand-alone device or together with a variety of cleared and unmodified syngo based software options. syngo.via View&GO supports interpretation and evaluation of examinations within healthcare institutions, for example, in Radiology, Nuclear Medicine and Cardiology environments. The system is not intended for the displaying of digital mammography images for diagnosis in the U.S. #### 6.2 Indications for Use syngo.via View&GO is indicated for image rendering and post-processing of DICOM images to support the interpretation in the field of radiology, nuclear medicine and cardiology. #### 6.3 Contraindications The system is not indicated for mammography images for diagnosis in the U.S. The application is not to be used as an archiving device for patients' image data. The application is not to be used as a sole basis for clinical decisions but further evidence has to be taken into account. #### 6.4 Patient Target Population syngo.via View&GO has neither limitations concerning the patient population (e.g. age, weight, health, condition) nor limitations concerning region of body or tissue type. {7}------------------------------------------------ # 7. Summary of Differences between the Subject Device and the Predicate Device: The following table compares the functionality of syngo.via View&GO VA40A to the predicate device syngo.via View&GO VA30A: | | Subject device | Predicate device | Comparison | Impact to Safety & Effectiveness | |----------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Device name and version (K number) | syngo .via View&GO (Version VA40A) | syngo .via View&GO Version VA30A (K221501) | New product version | NA | | Manufacturer | Siemens Healthcare GmbH | Siemens Healthcare GmbH | Identical | NA | | Intended use | syngo .via View&GO is a software solution intended to be used for viewing, manipulation, communication, and storage of medical images. It can be used as a stand- alone device or together with a variety of cleared and unmodified syngo based software options. syngo .via View&GO supports interpretation and evaluation of examinations within healthcare institutions, for example, in Radiology, Nuclear Medicine and Cardiology environments. The system is not intended for the displaying of digital mammography images for diagnosis in the U.S. | syngo .via View&GO is a software solution intended to be used for viewing, manipulation, communication, and storage of medical images. It can be used as a stand- alone device or together with a variety of cleared and unmodified syngo based software options. syngo .via View&GO supports interpretation and evaluation of examinations within healthcare institutions, for example, in Radiology, Nuclear Medicine and Cardiology environments. The system is not intended for the displaying of digital mammography images for diagnosis in the U.S. | Identical | NA | | Software architecture | Standalone workplace system that is logically broken down to syngo.via View&GO subsystems. Subsystems are further broken down to syngo modules. | Standalone workplace system that is logically broken down to syngo.via View&GO subsystems. Subsystems are further broken down to syngo modules. | Identical | NA | | Image communication | Standard network protocols like TCP/IP and standard communication protocol DICOM. | Standard network protocols like TCP/IP and standard communication protocol DICOM. | Identical | NA | | Imaging algorithms | - Multiplanar reconstruction (MPR) | - Multiplanar reconstruction (MPR) | Similar: Algorithms | The changes between the | | | Subject device | Predicate device | Comparison | Impact to Safety & Effectiveness | | | Maximum and Minimum Intensity Projection (MIP/MinIP) Volume Rendering Technique (VRT) with additional edge and surface enhancements and control over rendering parameters Shaded Surface Display (SSD) Digitally Reconstructed Radiograph Editor functionality (e.g. ClipBox) Auto-Contour Registration Anatomical registration Region growing Automatic Spine Labeling, also for ribs in CT thorax scans ("Rib labeling") Reprocessing X-ray projection images into 3D image and Topograms FASTAlign Cinematic VRT1 | Maximum and Minimum Intensity Projection (MIP/MinIP) Volume Rendering Technique (VRT) with additional edge and surface enhancements and control over rendering parameters Shaded Surface Display (SSD) Digitally Reconstructed Radiograph Editor functionality (e.g. ClipBox) Auto-Contour Registration Anatomical registration Region growing Automatic Spine Labeling, also for ribs in CT thorax scans ("Rib labeling") Reprocessing X-ray projection images into 3D image and Topograms FASTAlign | underwent bug- fixing and minor improvements. No re-training or change in algorithm models was performed. The cinematic VRT algorithm was added, that was previously cleared with K213665. | predicate device and the subject device doesn't impact the safety and effectiveness of the subject device as the necessary measures were taken for the safety and effectiveness of the subject device | | Quantitative algorithms | Distance, angle & angle- on-stack, VOI and ROI measurements | Distance, angle & angle- on-stack, VOI and ROI measurements | Identical | NA | | Supported Image Generating Modalities | The following Image types are supported by syngo.via View&GO: CT Image (Computed Tomography) MR Image (Magnetic Resonance) NM Image (Nuclear Medicine) XA Image (X-Ray Angiography) US Image (Ultrasound) DX Image (Digital Radiography) | The following Image types are supported by syngo.via View&GO: CT Image (Computed Tomography) MR Image (Magnetic Resonance) NM Image (Nuclear Medicine) XA Image (X-Ray Angiography) US Image (Ultrasound) DX Image (Digital Radiography) | Identical | NA | | | Subject device | Predicate device | Comparison | Impact to Safety & Effectiveness | | | DICOM secondary capture objects | DICOM secondary capture objects | | | | Image data Compression | Receive & Store: Images are received and stored as received without any change in the compression format. Display: Images are displayed as received without any change in the compression. Lossy compression images are displayed with an indication to the user with the compression ratio. Export: To DICOM Node: Images are sent as per the DICOM negotiation. Uncompressed is preferred and lossy compression is not supported. To Exchangeable media: Images exported as stored in the local storage. Supported Compressions for export: lossless compression algorithms, JPEG, JPEG 2000 and RLE. | Receive & Store: Images are received and stored as received without any change in the compression format. Display: Images are displayed as received without any change in the compression. Lossy compression images are displayed with an indication to the user with the compression ratio. Export: To DICOM Node: Images are sent as per the DICOM negotiation. Uncompressed is preferred and lossy compression is not supported. To Exchangeable media: Images exported as stored in the local storage. Supported Compressions for export: lossless compression algorithms, JPEG, JPEG 2000 and RLE. | Identical | NA | | Operating system | Workplace: Microsoft Windows 11-64 bit or higher Microsoft Windows 10 - 64 bit or higher | Workplace: Microsoft Windows 10 - 64 bit or higher Microsoft Windows 7 - 64 bit SP1 (for update only) | Windows 11 support included. Windows 7 support was removed | The changes between the predicate device and the subject device don't impact the safety and effectiveness of the subject device as the necessary measures were taken for the safety and effectiveness of the subject device | | | Subject device | Predicate device | Comparison | Impact to Safety & Effectiveness | | Impact on Image Generating Devices | None. syngo.via View&GO is a pure post processing software and there is no influence on the image generating devices | None. syngo.via View&GO is a pure post processing software and there is no influence on the image generating devices | NA as both the devices do not impact the Image generating devices. | NA | | CAD Functionalities | None. No automated diagnostic interpretation capabilities like CAD are included. All image data are to be interpreted by trained personnel. | None. No automated diagnostic interpretation capabilities like CAD are included. All image data are to be interpreted by trained personnel. | NA as both the devices don't support any CAD functionalities. | NA | | Software self-test / checks | Alert the user in case the data transfer is interrupted to the connected DICOM node. Hardware / Operating system compatibility check during Installation. Display Compatibility Check supports the end user to qualify the system for proper diagnostic use. | Alert the user in case the data transfer is interrupted to the connected DICOM node. Hardware / Operating system compatibility check during Installation. Display Compatibility Check supports the end user to qualify the system for proper diagnostic use. | Identical | NA | | Cyber Security | - User access control - Audit trails - Documentation of system security information, Network traffic & Firewall control - Support of virus / malware protection. | - User access control - Audit trails - Documentation of system security information, Network traffic & Firewall control - Support of virus / malware protection. | Identical | NA | | Hardware | Hardware is not understood as part of the medical device but needs to comply with the minimum requirements as specified by syngo.via View&GO. | Hardware is not understood as part of the medical device but needs to comply with the minimum requirements as specified by syngo.via View&GO. | Identical | NA | | Software | | | | | | | Subject device | Predicate device | Comparison | Impact to Safety & Effectiveness | | Graphical User Interface | Yes, with reduced color palette, clearer structure and text labels on icons. | Yes, with reduced color palette, clearer structure and text labels on icons | Identical | NA | | Patient Browser | Yes, with simplified search functionality, clearer structure of search results, image preview, unlimited search results, periodic updates of search results. | Yes, with simplified search functionality, clearer structure of search results, image preview, unlimited search results, periodic updates of search results. | Identical | NA | | Series navigator | The Series Navigator lists all currently loaded data within a workflow. Studies are marked with colorized timepoints. | Yes, the Series Navigator lists all currently loaded data within a workflow. Studies are marked as "prior" and "current" according to their acquisition date. | To improve the visualization of studies according to their different timepoints of acquisition, the timepoints are shown in dates of different colors and the study date is featured more prominently with larger and bold font in the subject device. | The changes between the predicate device and the subject device don't impact the safety and effectiveness of the subject device as the necessary measures were taken for the safety and effectiveness of the subject device. The functionality was previously cleared with additional reference device K213665. | | Findings / Reporting | No, reporting support is provided to create reports using any 3rd party reporting tool. Hence the findings also cannot be navigated. | No, reporting support is provided to create reports using any 3rd party reporting tool. Hence the findings also cannot be navigated. | Identical | NA | | Import and export of data | Import of DICOM data from network nodes or external media, and of DICOM-compliant or non DICOM-compliant data from external media and Windows file system. Export to USB, Windows file system, or other DICOM nodes. | Import of DICOM data from network nodes or external media, and of DICOM-compliant or non DICOM-compliant data from external media and Windows file system. Export to USB, Windows file system, or other DICOM nodes. | Identical | NA | | Archiving data | Data can be sent to an archive if syngo.via | Data can be sent to an archive if syngo.via | Identical | NA | | | Subject device | Predicate device | Comparison | Impact to Safety & Effectiveness | | | View&GO is connected to a PACS or corresponding DICOM node.…

syngo.via View&GO VA40A

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syngo.via View&GO VA40A

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