(127 days)
Not Found
No
The document describes standard radiation therapy linear accelerator systems and associated software for treatment planning, delivery, and image processing. There is no mention of AI, ML, or related concepts in the intended use, device description, or performance studies.
Yes
The document states that the intended use of the SIEMENS linear accelerator systems is "to deliver X-ray photon and electron radiation for the therapeutic treatment of cancer." This explicitly indicates a therapeutic purpose.
No
The device is primarily a linear accelerator system for therapeutic treatment of cancer, specifically delivering X-ray photon and electron radiation. While it includes software for viewing, processing, and archiving medical images, and aids in the "diagnosis, staging, and prescription of radiation therapy," its fundamental purpose as described in the "Intended Use" is for treatment, not diagnostic imaging to identify or characterize disease. The "syngo@RT Oncologist Workspace" aids in diagnosis, but the overall product is a treatment delivery system for radiation therapy.
No
The device description explicitly states it is an "Update to the ARTISTE family of medical linear accelerators" and mentions interfacing with "third party devices conforming to the DICOM Standard," indicating it is part of a larger hardware system (linear accelerators) and not solely software.
Based on the provided text, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The primary intended use is to deliver radiation for the therapeutic treatment of cancer. This is a therapeutic device, not a diagnostic one.
- Device Description: The device is a linear accelerator system and associated software for treatment planning, delivery, and verification. While it involves image processing, this is for the purpose of guiding and verifying radiation therapy, not for diagnosing a condition based on in vitro samples.
- No mention of in vitro samples: The text does not mention the analysis of any biological samples (blood, urine, tissue, etc.) which is a key characteristic of IVD devices.
The software components mentioned are for managing patient data, processing medical images (likely for treatment planning and verification), and aiding in the delivery of radiation therapy. These functions are all related to the therapeutic process, not in vitro diagnosis.
N/A
Intended Use / Indications for Use
The intended use of the SIEMENS branded ARTISTE™. ONCOR™ and PRIMUS™ family of linear accelerator systems is to deliver X-ray photon and electron radiation for the therapeutic treatment of cancer.
The linear accelerator systems are high-dose and high-dose rate medical linear accelerators optimized for 3D conformal radiation therapy, intensity-modulated radiation therapy (IMRT) and precision stereotactic applications. The stereotactic applications may include single-session radiosurgery, fractionated stereotactic radiation therapy, or fractionated stereotactic intensity modulated radiation therapy for lesions, tumors and conditions anywhere in the head and body where radiation therapy is indicated.
The syngo® workspaces includes a number of syngo® based software applications whose indication for use include the viewing, processing, filming, and archiving of medical images. The workspaces also permit patient data management, patient selection/setup, patient positioning verification, treatment planning, treatment delivery/verification, and treatment recording.
The syngo® RT Therapist Connect Workspace v4.2, contains software applications that permits patient selection/setup, patient positioning verification, treatment delivery/verification, and treatment recording. The syngo® RT Therapist Connect Workspace v4.2, can be interfaced with third party devices conforming to the DICOM Standard.
The syngo@RT Oncologist Workspace permits localization, contouring, segmentation, image calibration, and review of treatment plan parameters. In addition, it includes tools and administrative functions to aid in the diagnosis, staging, and prescription of radiation therapy.
Product codes
IYE
Device Description
The ARTISTE™ Solution SYS_VB50 Update to the ARTISTE family of medical linear accelerators is intend to update customers with optional new features and accessories for systems with the syngo® RT Therapist and RT Therapist Connect Workspaces (versions v4.1 or v4.2) for the ARTISTE systems. This update is intended to be backwards compatible to the currently cleared ONCOR and PRIMUS family of medical linear accelerators and their Control Consoles (v9.0+ and v11.0+), the RT Therapist (v2.1a or v2.2) and Oncologist v2.0 workspaces.
The technological characteristics of the RT Therapist Connect Workspace v4.2 and Control Console 12 remain unchanged from the currently cleared product (K102671).
The syngo® Suite for Oncology Workspace focused software utilizes the proprietary syngo® software architecture design provides a method of delivering customized software applications based on the modality as clinically supporting packages. From these applications SIEMENS utilizes, as part of the Oncology clinical focus package, multiple applications for patient set-up and position verification, treatment localization, treatment verification, portal imaging as well as data processing, image reformatting, display and printing. The currently cleared COHERENCE™ and syngo® products also include an array of image-oriented software tools, support for DICOM connectivity and the Siemens Remote Service option.
Mentions image processing
Yes
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
head and body
Indicated Patient Age Range
Not Found
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
Bench testing in the form of Unit, Sub-System Integration (SSIT), and System Integration (SIT) testing was performed to evaluate the performance and functionality of the new feature and software updates. All testable requirements in the Engineering Requirements Specifications (ERS) keys, Sub-System Requirements Specifications (SSRS) keys, and the Risk Management Hazard keys have been successfully verified and traced in accordance with the Siemens product development (lifecycle) process (PDP).
The software verification and regression testing has been performed successfully to meet their previously determined acceptance criteria as stated in the Test Plans.
Validation of the new features for syngo® RT Therapist Connect Workspace, v4.2 and Oncologist v4.2 has been performed at the System test (ST) level on production prototype devices by appropriately trained and knowledgeable test personnel. System level validation and regression testing has been performed successfully, demonstrating that the software meets the acceptance criteria as noted in the system test plans.
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
The verification testing to the new software features and component requirements for
- In-Line kView™ imaging with the carbon graphite target and the OPTIVUE™ . 1000ART Flat Panel,
- . the additional high dose rate Unflat energies in Multiple X™.
- the syngo® RT Oncologist v4 with Adaptive Targeting, Advanced and Model ● Based Segmentation and 3D Image and plan review and approval,
- . accessories such as Small cones, Rotational applicators,
- and the OPTIGARD™ collision avoidance system, .
- along with the validation of the intended use,
including the regression testing to the existing RT Therapist Connect software v4.2 and the Control Console 12 functional requirements, is intended to support the claim of substantial equivalence to the currently cleared: - syngo® RT Therapist Connect Workspace, v4.2(K102671), ●
- the ARTISTE (K072485) medical linear accelerator with the RT Therapist and . RT Therapist Assist workspaces, electron cone accessories and a collision avoidance system.
- and to the stereotactic option PreScision (K082775) for high dose rate, unflat energies.
- additionally to the Advanced Segmentation and Model based Segmentation . features in the Dosimetrist v2.7 (K101119)
- Image and plan review and approval and Adaptive Targeting in the Oncologist . v2.0 (K060633)
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.
K102671, K072485, K060633, K101119, K082775
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
§ 892.5050 Medical charged-particle radiation therapy system.
(a)
Identification. A medical charged-particle radiation therapy system is a device that produces by acceleration high energy charged particles (e.g., electrons and protons) intended for use in radiation therapy. This generic type of device may include signal analysis and display equipment, patient and equipment supports, treatment planning computer programs, component parts, and accessories.(b)
Classification. Class II. When intended for use as a quality control system, the film dosimetry system (film scanning system) included as an accessory to the device described in paragraph (a) of this section, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 892.9.
0
. .
. .
ు
Siemens Medical Solutions USA, Inc. Oncology Care Systems
APR 15 2011
November 27, 2010
Section 5
510(k) Summary ::
..
Date Prepared: ·
Submitter: Siemens Medical Solutions USA, Inc. Oncology Care Systems 4040 Nelson Avenue . Concord, CA 94520
Contact: Christine Dünbar Senior Regulatory Affairs Specialist
Phone: (925) 602-8157 Fax: . (925) 602-8008 Email: christine.dunbar@siemens.com
Proprietary Name: ARTISTE™ Solution with SYS_VB50 Update
Medical Charged-Particle Radiation Therapy System Common Name:
Classification: 892.5050
Product Code: IYE
Substantial Equivalence Claimed To:
| Product | 510(k)
Clearance
/Date | Claim of Equivalence for: |
|-------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| syngo® RT Therapist
Connect for RT
Therapist version 4.2
including Control
Console 12. | K102671 /
Oct. 12,
2010 | syngo® RT Therapist Connect v4.2 software update
SYS_VB50 and Control Console 12, and new
licensed features, In-Line kView™ and Multiple
X™ |
| ARTISTE™ Solution
(aka ARTISTE MV)
RTT v4.1 with
MegaVoltage Cone
Beam (MVCB) and the
OPTIVUE Flat Panel,
160MLC and electron | K072485 /
Dec. 27,
2007 | ARTISTE™ Solution with the syngo® RT Therapist
Connect v4.2 with software update SYS_VB50 and
Control Console 12, with the new licensed feature
In-Line kView™ using the MVCB with a carbon
graphite target, OPTIVUE 1000ART Flat Panel,
160MLC and electron treatment cones and |
. ..
510(k) for SIEMENS ARTISTE™ Solution with SYS_VB50 Update
Page Sect. 5/1
00023
1
| Product | 510(k)
Clearance/
Date | Claim of Equivalence for: |
|----------------------------------------------------------------------------------------------------------------------|-------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| treatment cones and
accessories
Including the RT
Therapist Assist (off-
line) Workspace | | accessories
syngo® RT Oncologist v4.2 including the RT
Therapist Assist off-line features. |
| COHERENCE™
Oncologist v2.0 with
Adaptive Targeting and
2D portal image
approval. | K060633 /
May 01,
2006 | syngo® RT Oncologist v4.2 with Adaptive
Targeting and 3D portal image approval. |
| syngo® Dosimetrist
Workspace v2.7
including the Basic,
Advance and Model
based Segmentation
features. | K101119 /
June 16,
2010 | syngo® RT Oncologist v4.2 with Basic, Advance
and Model based Segmentation features. |
| PreScision™ Option* | K082775 /
Feb. 19,
2009 | ARTISTE™ Solution with the syngo® RT Therapist
Connect v4.2 with software update SYS_VB50 and
Control Console 12, and new licensed feature called
Multiple X™ and multiple high dose rate and
UnFlat energy options. |
The ARTISTETM Solution SYS VB50 Update as described in this premarket notification has the same intended use and fundamental scientific technical characteristics as the predicate devices listed above.
Description Summary - ARTISTE™ Solution with SYS_VB50 Update
Technological Characteristics:
The ARTISTE™ Solution SYS_VB50 Update to the ARTISTE family of medical linear
accelerators is intend to update customers with optional new features and accessories for systems with the syngo® RT Therapist and RT Therapist Connect Workspaces (versions v4.1 or v4.2) for the ARTISTE systems. This update is intended to be backwards compatible to the currently cleared ONCOR and PRIMUS family of medical linear accelerators and their Control Consoles (v9.0+ and v11.0+), the RT Therapist (v2.1a or v2.2) and Oncologist v2.0 workspaces.
The technological characteristics of the RT Therapist Connect Workspace v4.2 and Control Console 12 remain unchanged from the currently cleared product (K102671).
510(k) for SIEMENS ARTISTE™ Solution with SYS VB50 Update
2
The syngo® Software Architecture:
The syngo® Suite for Oncology Workspace focused software utilizes the proprietary syngo® software architecture design provides a method of delivering customized software applications based on the modality as clinically supporting packages. From these applications SIEMENS utilizes, as part of the Oncology clinical focus package, multiple applications for patient set-up and position verification, treatment localization, treatment verification, portal imaging as well as data processing, image reformatting, display and printing. The currently cleared COHERENCE™ and syngo® products also include an array of image-oriented software tools, support for DICOM connectivity and the Siemens Remote Service option.
Refer to Section 11- Description, for the Product and Sub-System Requirements Specifications regarding these specific requirements.
General Safety and Effectiveness:
The device labeling contains instructions for use and any necessary cautions and warnings, 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 and mitigations. These potential hazards are controlled by software means, user instructions, verification of requirements and validation of the clinical workflow to ensure that the product meets its intended uses. To minimize electrical, mechanical and radiation hazards, SIEMENS adheres to recognized and established industry practice and relevant international standards.
Refer to Section 21 for the Risk Management documentation.
Intended Use:
The intended use of the SIEMENS branded ARTISTE™. ONCOR™ and PRIMUS™ family of linear accelerator systems is to deliver X-ray photon and electron radiation for the therapeutic treatment of cancer.
The linear accelerator systems are high-dose and high-dose rate medical linear accelerators optimized for 3D conformal radiation therapy, intensity-modulated radiation therapy (IMRT) and precision stereotactic applications. The stereotactic applications may include single-session radiosurgery, fractionated stereotactic radiation therapy, or fractionated stereotactic intensity modulated radiation therapy for lesions, tumors and conditions anywhere in the head and body where radiation therapy is indicated.
The syngo® Suite for Oncology Workspaces:
The syngo® workspaces includes a number of syngo® based software applications whose indication for use include the viewing, processing, filming, and archiving of medical images. The
510(k) for SIEMENS ARTISTE™ Solution with SYS VB50 Update
Page Sect. 5/3
3
workspaces also permit patient data management, patient selection/setup, patient positioning verification, treatment planning, treatment delivery/verification, and treatment recording.
The syngo@RT Therapist Connect Workspace v4.2, contains software applications that permits patient selection/setup, patient positioning verification, treatment delivery/verification, and treatment recording. The syngo® RT Therapist Connect Workspace v4.2, can be interfaced with third party devices conforming to the DICOM Standard.
The syngo® RT Oncologist Workspace v4.2 permits localization, contouring, segmentation, image calibration, and review of treatment plan parameters. In addition, it includes tools and administrative functions to aid in the diagnosis, staging, and prescription of radiation therapy.
Substantial Equivalence:
The Substantial Equivalence comparison chart in Section 12 demonstrates the comparison of the technological characteristics of the new features and their currently cleared predicate devices.
The new features for the syngo® RTT Connect Workspace v4.2, the rebranding and updating of the syngo® RT Oncologist v4.2 and the modifications to the Linear Accelerator portal imaging system, does not change the intended use of the original syngo® RT Therapist or Oncologist Workspaces or the Siemens branded Linear Accelerator Systems.
Bench Testing:
Bench testing in the form of Unit, Sub-System Integration (SSIT), and System Integration (SIT) testing was performed to evaluate the performance and functionality of the new feature and software updates. All testable requirements in the Engineering Requirements Specifications (ERS) keys, Sub-System Requirements Specifications (SSRS) keys, and the Risk Management Hazard keys have been successfully verified and traced in accordance with the Siemens product development (lifecycle) process (PDP).
The software verification and regression testing has been performed successfully to meet their previously determined acceptance criteria as stated in the Test Plans.
Non-Clinical Test Results:
Validation of the new features for syngo® RT Therapist Connect Workspace, v4.2 and Oncologist v4.2 has been performed at the System test (ST) level on production prototype devices by appropriately trained and knowledgeable test personnel. System level validation and regression testing has been performed successfully, demonstrating that the software meets the acceptance criteria as noted in the system test plans.
Testing to Consensus Standards:
510(k) for SIEMENS ARTISTE™ Solution with SYS VB50 Update
Page Sect. 5/4
00026
4
The Siemens branded Linear Accelerators with the new features have been tested to meet the requirements for conformity (where applicable) to multiple industry standards. Refer to Sections 9 and 17 for this content.
Substantial Equivalence to Predicates:
The verification testing to the new software features and component requirements for
- In-Line kView™ imaging with the carbon graphite target and the OPTIVUE™ . 1000ART Flat Panel,
- . the additional high dose rate Unflat energies in Multiple X™.
- the syngo® RT Oncologist v4 with Adaptive Targeting, Advanced and Model ● Based Segmentation and 3D Image and plan review and approval,
- . accessories such as Small cones, Rotational applicators,
- and the OPTIGARD™ collision avoidance system, .
- along with the validation of the intended use,
including the regression testing to the existing RT Therapist Connect software v4.2 and the Control Console 12 functional requirements, is intended to support the claim of substantial equivalence to the currently cleared:
- syngo® RT Therapist Connect Workspace, v4.2(K102671), ●
- the ARTISTE (K072485) medical linear accelerator with the RT Therapist and . RT Therapist Assist workspaces, electron cone accessories and a collision avoidance system.
- and to the stereotactic option PreScision (K082775) for high dose rate, unflat energies.
- additionally to the Advanced Segmentation and Model based Segmentation . features in the Dosimetrist v2.7 (K101119)
- Image and plan review and approval and Adaptive Targeting in the Oncologist . v2.0 (K060633)
Summary:
. ·
In summary, it is SIEMENS' belief that the ARTISTE with the Sys VB50 update does not introduce any new potential safety risks and is substantially equivalent to, and performs as well as the predicate devices.
Page Sect. 5/5
00027
5
Image /page/5/Picture/0 description: The image shows the seal of the U.S. Department of Health and Human Services. The seal features a stylized caduceus, a symbol often associated with medicine and healthcare, in the center. The words "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" are arranged in a circular pattern around the caduceus. The seal is simple and monochromatic.
DEPARTMENT OF HEALTH & HUMAN SERVICES
Public Health Service
Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -- WO66-G609 Silver Spring, MD 20993-0002
Ms. Christine Dunbar Senior Regulatory Affairs Specialist Siemens Medical Solutions USA, Inc. Oncology Care Systems 4040 Nelson Avenue CONCORD CA 94520
APR 1 5 2011
Re: K103606
Trade/Device Name: ARTISTE™ Solution with SYS VB50 Update Regulation Number: 21 CFR 892.5050 Regulation Name: Medical charged-particle radiation therapy system Regulatory Class: II Product Code: IYE Dated: March 25, 2011 Received: March 28, 2011
Dear Ms. Dunbar:
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 class II (Special Controls), it may be subject to such additional controls. Existing major regulations affecting your device can be found in Title 21, Code of Federal Regulations (CFR), Parts 800 to 895. 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 Parts 801 and 809); medical device reporting (reporting of
6
Page 2
medical device-related adverse events) (21 CFR 803); and good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820). 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 Parts 801 and 809), please contact the Office of In Vitro Diagnostic Device Evaluation and Safety at (301) 796-5450. 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
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
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 (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely Yours.
Mary Patel
Mary S. Pastel, Sc.D. Director Division of Radiological Devices Office of In Vitro Diagnostic Device Evaluation and Safety Center for Devices and Radiological Health
Enclosure
7
Section 4
Indication For Use Statement
510(k) Number (if known): K (03606
Device Name: ARTISTE™ Solution with SYS VB50 Update
Indications for Use:
The intended use of the SIEMENS branded ARTISTE™, ONCOR™ and PRIMUS™ family of linear accelerator systems is to deliver X-ray photon and electron radiation for the therapeutic treatment of cancer.
The linear accelerator systems are high-dose and high-dose rate medical linear accelerators optimized for 3D conformal radiation therapy, intensity-modulated radiation therapy (IMRT) and precision stereotactic applications. The stereotactic applications may include single-session radiosurgery, fractionated stereotactic radiation therapy, or fractionated stereotactic intensity modulated radiation therapy for lesions, tumors and conditions anywhere in the head and body where radiation therapy is indicated.
The syngo® Suite for Oncology Workspaces:
The syngo® workspaces includes a number of syngo® based software applications whose indication for use include the viewing, processing, filming, and archiving of medical images. The workspaces also permit patient data management, patient selection/setup, patient positioning verification, treatment planning, treatment delivery/verification, and treatment recording.
The syngo® RT Therapist Connect Workspace v4.2, contains software applications that permits patient selection/setup, patient positioning verification, treatment delivery/verification, and treatment recording. The syngo® RT Therapist Connect Workspace v4.2, can be interfaced with third party devices conforming to the DICOM Standard.
The syngo@RT Oncologist Workspace permits localization, contouring, segmentation, image calibration, and review of treatment plan parameters. In addition, it includes tools and administrative functions to aid in the diagnosis, staging, and prescription of radiation therapy.
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of In Vitro Diagnostic Devices (OIVD)
| (Division Sign-Off) | |
|---|---|
| Division of Radiological Devices | |
| Office of In Vitro Diagnostic Device Evaluation and Safety |
| 510K | K113606 |
|---|---|
| Prescription Use | ✓ |
| (Per 21 CFR 801.109) | |
| OR | |
| Over-the-Counter Use |
510(k) for SIEMENS ARTISTE™ Solution with SYS VB50 Update
Page Sec 4/1
00022