SYNGO IMAGING (VERSION V30)

K071114 · Siemens AG Medical Solutions · LLZ · May 22, 2007 · Radiology

Device Facts

• Record ID: K071114
• Device Name: SYNGO IMAGING (VERSION V30)
• Applicant: Siemens AG Medical Solutions
• Product Code: LLZ · Radiology
• Decision Date: May 22, 2007
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 892.2050
• Device Class: Class 2
• Attributes: Software as a Medical Device, 3rd-Party Reviewed

Intended Use

syngo® Imaging is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital radiological images, including digital mammography images. It supports the physician in diagnosis and treatment planning. For primary image diagnosis in mammography only uncompressed or non-lossy compressed images and only pre-processed DICOM "For Presentation" images must be used. Also only monitors which received FDA approval for mammography must be used. syngo® Imaging also supports storage and archiving of DICOM Structured Reports. In a comprehensive imaging suite syngo® Imaging integrates Radiology Information Systems (RIS) to enable customer specific workflows.

Device Story

syngo® Imaging V30 is a PACS for radiological image management. Inputs include digital radiological images (including mammography) and DICOM structured reports. System integrates with RIS via HL7/DICOM to support clinical workflows. Operates as a software-only solution or on certified IT hardware; used by physicians and technicians in radiology suites or clinical settings. Provides tools for viewing, post-processing, reporting, and distribution. Advanced studio bundles include specialized applications like CT Colonography. Output is displayed on FDA-approved monitors for diagnostic review. Benefits include centralized data access, improved workflow efficiency, and support for clinical decision-making through advanced visualization and reporting tools.

Clinical Evidence

Bench testing only. Verification and validation testing performed to ensure software safety and effectiveness. Risk management analysis conducted to identify and control potential hazards.

Technological Characteristics

Software-only PACS; runs on Windows XP (workstations) and Linux/Windows 2003 (backend). Supports DICOM image/object standards. Hardware-independent but requires predefined minimum specs. High availability via redundant hardware and cluster software. Integration with RIS via HL7/DICOM (IHE Year 5).

Indications for Use

Indicated for use by physicians and radiological technicians for the display, processing, reading, reporting, communication, distribution, storage, and archiving of digital radiological images, including digital mammography. Supports diagnosis and treatment planning. For mammography primary diagnosis, requires uncompressed or non-lossy compressed images, pre-processed DICOM "For Presentation" images, and FDA-approved mammography monitors.

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 Imaging (K052401)
• syngo MultiModality Workplace (K061964)

Reference Devices

• syngo® CT Colonography (K042605)
• syngo® WebSpace (K062673)
• Siemens AG SMVD 21500 (K043122)
• Dj(S)-2103-D-5MP (K043122)

Submission Summary (Full Text)

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Ko71114

MAY 2 2 2007

### 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.

### I. GENERAL INFORMATION

#### Establishment:

| • Address: | Siemens AG, Medical Solutions<br>Henkestrasse 127<br>D-91052 Erlangen<br>Germany |
|------------|----------------------------------------------------------------------------------|
|------------|----------------------------------------------------------------------------------|

- . Registration Number: 3002808157

| Contact Person: | Eva Reiter |
|-----------------|-------------------------------|
| | Regulatory Affairs Manager |
| | Telephone: [phone] |
| | Telefax: [phone] |

Device Name and Classification:

| • Trade Name: | syngo® Imaging<br>Version V30 |
|-------------------------|---------------------------------------------|
| • Classification Name: | Picture Archiving and Communications System |
| • Classification Panel: | Radiology |
| • CFR Section: | 21 CFR §892.2050 |
| • Device Class: | Class II |
| • Product Code: | LLZ |

# II. SAFETY AND EFFECTIVENESS INFORMATION SUPPORTING THE SUBSTANTIAL EQUIVALENCE DETERMINATION

#### Device Description and Intended Use: .

This premarket notification covers Siemens´ enhanced PACS system syngo® Imaging, version V30.

syngo® Imaging is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital rediological images, including digital mammography images.

It supports the physician in diagnosis and treatment planning.

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For primary image diagnosis in mammography only uncompressed or non-lossy compressed images and only pre-processed DICOM "For Presentation" images must be used. Also only monitors which received FDA approval for mammography must be used,

syngo® Imaging also supports storage and archiving of Structured DICOM Reports.

In a comprehensive imaging suite syngo® Imaging integrates Radiology Information Systems (RIS) to enable customer specific workflows. especially by supporting the role based and context sensitive RIS portals (such as "Portal Radiologist"). Enhanced syngo® Imaging workplaces use a variety of advanced post processing applications.

The system is a "hardware independent" solution to be distributed either as software only or combined with common IT hardware which must comply to predefined minimum hardware requirements.

The version V30 contains multiple improvements and optimizations on front end for usability, such as layout enhancements and display improvements.

# syngo® Imaging Workplaces

The three syngo® Imaging workplace deployments ...

- syngo® Web Studio a web-based viewing application mainly used for image distribution a)
- b) syngo® Basic Studio - for basic reporting, inside as well as outside of the radiology (standalone workstation)
- syngo® Advanced Studio Advanced Application Bundle for use inside the radiology c) with advanced reporting functionality

... are medical diagnostic and viewing workstations intended for post processing, reporting, viewing and communicating / distributing of radiological softcopy images (including digital mammographic images) and so allow radiological technicians to receive and process all data needed.

Based on Siemens syngo® software, the syngo® Imaging supports the wide variety of image types and its modular design and is capable of combining applications from different modalities in one workstation.

The syngo® Advanced Studio integrates the modality specific application package syngo® CT Colonography (K042605).

The syngo Imaging supports external post processing via the OEM interface by integration of the 314 party application syngo® WebSpace (K062673).

By usage of only specific FDA approved monitors (e.g Siemens AG: SMVD 21500 or Dj(S)}-2103-D-5MP - K043122) validated together with the software, diagnosis on digital mammography images is possible, if images are not compressed lossy, as disclaimed respectively.

### syngo® Imaging Data Management

... ensures all authorized personnel fast and continuous access to radiological data. It's main functionality ranges from availability of images having regard to data security, open interfaces, storage media, central system administration, back-up, software distribution to providing a flexible storage hierarchy.

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The main purpose is storing and archiving of radiological softcopy images and structured (DICOM) reports.

For PACS server the syngo® Imaging Data Management can be used as a DIC ()M-Archive (LTS Long-term Storage) in accordance with the DIC()M Conformance Statement.

# Integration:

The Workflow Management enables by integration of any HL7- / DICOM-compatible RIS (IHE Year 5) to the syngo® Imaging PACS a consistent workflow – from patient revisuration to requirement scheduling to a personal work list and supports therefore reporting, documentation or administrative tasks.

#### . Technological Characteristics:

syngo® Imaging (version V30) is a "software only"-system, which will be delivered on CD-ROM / DVD or as a complete radiology solution consisting of common IT hardware and preinstalled software. syngo® Imaging will be installed by Siemens service engineers.

Defined Hardware requirements are to be met.

The backend communication and storage solution (DM) is based on LINUX and Windows 2003 operating system. The workplaces are based on Windows XP. Any hardware platform, which is Windows / Windows XP certified, will be supported.

The herewith described syngo® Imaging supports DICOM formatted images and objects.

By usage of redundant hardware component and cluster software a high availability concept could be realized, which provides as less as possible system downtime.

#### . General Safety and Effectiveness Concerns:

The device labelling contains instructions for use and any necessary cautions and warning, to provide for safe and effective use of the device.

Risk management is ensured via a risk analysis, which is used to identify potential hazards. These potential hazards are controlled via software development, verification and validation testing. To minimize electrical, mechanical, and radiation hazards, Siemens adheres to recognized and established industry practice and standards.

#### . Substantial Equivalence:

The syngo® Imaging, addressed in this premarket notification, is substantially equivalent to the following commercially available devices:

| Siemens | syngo Imaging | K05240i |
|---------|-------------------------------|---------|
| Siemens | syngo MultiModality Workplace | K061964 |

The syngo® Imaging described in this 510(k) has the same intended use and similar technical characteristics as the devices listed above in regard to the specific functionalities.

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In summary, Siemens is of the opinion that syngo® Imaging does not introduce any new potential safety risks and is substantially equivalent to and performs as well as the predicate devices.

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Image /page/4/Picture/1 description: The image shows the address of the Food and Drug Administration. The address is 9200 Corporate Blvd., Rockville MD 20850. The text is black and the background is white.

Siemens AG c/o Olaf Teichert Third Party Reviewer TÜV Product Service 1775 Old Highway 8 N.W., Ste. 104 NEW BRIGHTON MN 55112-1891

MAY 2 2 2007

Re: K071114

Trade/Device Name: syngo® Imaging (version V30) Regulation Number: 21 CFR §892.2050 Regulation Name: Picture archiving and communications system Regulatory Class: II Product Code: LLZ Dated: May 4, 2007 Received: May 9, 2007

Dear Mr. Teichert:

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. 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.

If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may be subject to such 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.

Image /page/4/Picture/9 description: The image shows a logo with the text "1906-2006 FDA Centennial" in a circular arrangement. The acronym "FDA" is prominently displayed in the center of the logo. The logo also includes three stars below the word "Centennial". The text is arranged in a circular fashion around the acronym.

Protecting and Promoting Public Health

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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); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

This letter will allow you to begin marketing your device as described in your Section 510(k) . premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at one of the following numbers, based on the regulation number at the top of this letter:

| 21 CFR 876.xxxx | (Gastroenterology/Renal/Urology) | 240-276-0115 |
|-----------------|----------------------------------|--------------|
| 21 CFR 884.xxxx | (Obstetrics/Gynecology) | 240-276-0115 |
| 21 CFR 892.xxxx | (Radiology) | 240-276-0120 |
| Other | | 240-276-0100 |

Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number [phone] or [phone] or at its Internet address

http://www.fda.gov/cdrh/industry/support/index.html

Sincerely yours,

Nancy C. Brogdon

Nancy C. Brogdon Director, Division of Reproductive, Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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#### INDICATIONS FOR USE

510(k) Number (if known): Device Name: _________________________________________________________________________________________________________________________________________________________________

Indications For Use:

syngo® Imaging is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital radiological images, including digital mammography images.

It supports the physician in diagnosis and treatment planning.

For primary image diagnosis in mammography only uncompressed or non-lossy compressed images and only pre-processed DICOM "For Presentation" images must be used. Also only monitors which received FDA approval for mammography must be used. syngo® Imaging also supports storage and archiving of DICOM Structured Reports.

In a comprehensive imaging suite syngo® Imaging integrates Radiology Information Systems (RIS) to enable customer specific workflows.

Enhanced syngo® Imaging workplaces use a variety of advanced postprocessing applications.

X Prescription Use (Part 21 CFR 801 Subpart D)

AND / OR

Over-The-Counter Use (Part 21 CFR 801 Subpart C)

(Please do not write below this line - continue on another page if needed)

Concurrence of the CDRH, Office of Device Evaluation (ODE)

| | Nancy C Brogdon |
|--|---------------------|
| | (Division Sign-Off) |

Division of Reproductive, Abdominal, and
Radiological Devices

| 510(k) Number | K071114 |
|---------------|----------------|
| | March 31, 2007 |

| (k) for syngo® Imaging | Page A 1 |
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510(k) for syngo® Imaging