TrueBeam-TrueBeam STx-Edge

K143224 · Varian Medical Systems, Inc. · IYE · Dec 19, 2014 · Radiology

Device Facts

• Record ID: K143224
• Device Name: TrueBeam-TrueBeam STx-Edge
• Applicant: Varian Medical Systems, Inc.
• Product Code: IYE · Radiology
• Decision Date: Dec 19, 2014
• Decision: SESE
• Submission Type: Special
• Regulation: 21 CFR 892.5050
• Device Class: Class 2
• Attributes: Therapeutic, Pediatric

Indications for Use

The TrueBeam TM system is intended to provide stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body where radiation treatment is indicated.

Device Story

TrueBeam and Edge Radiotherapy Delivery Systems are medical linear accelerators for stereotactic radiosurgery and precision radiotherapy. The system integrates photon, electron, and diagnostic kV X-ray beam-producing components installed in a radiation-shielded vault with a control console located outside the treatment room. Operated by trained clinicians, the device delivers radiation to treat tumors and lesions throughout the body. The system utilizes an 80-leaf multi-leaf collimator (MLC) and manual bolus verification to shape and target radiation beams. By precisely delivering radiation, the device aims to destroy or control malignant and benign growths while sparing surrounding healthy tissue. Clinical decision-making is supported by the system's ability to perform image-guided radiotherapy, allowing providers to visualize and adjust treatment based on patient anatomy.

Clinical Evidence

No clinical data provided. Substantial equivalence is supported by bench testing, including hardware and software verification and validation, biocompatibility evaluation per ISO 10993-1, and electrical safety/EMC testing per IEC 60601-1 and IEC 60601-1-2 standards.

Technological Characteristics

Medical linear accelerator; photon, electron, and kV X-ray sources. Features 80-leaf MLC and manual bolus verification. Complies with IEC 60601-1 (safety), IEC 60601-1-2 (EMC), IEC 60601-2-1, IEC 60601-2-32, IEC 60601-2-44, IEC 61217, IEC 62304, IEC 62274, IEC 62366, IEC 60825, and IEC 60976. Biocompatibility per ISO 10993-1.

Indications for Use

Indicated for stereotactic radiosurgery and precision radiotherapy in adults and pediatric patients for lesions, tumors, and conditions including brain/spine tumors, head/neck, thoracic, gynecologic, gastrointestinal, genitourinary, breast, sarcomas, lymphoid, skin cancers, benign diseases (e.g., AVM, trigeminal neuralgia), and metastases.

Regulatory Classification

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.

Predicate Devices

• TrueBeam Radiotherapy System and Accessories (K140528)

Submission Summary (Full Text)

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Image /page/0/Picture/1 description: The image shows the logo for the Department of Health & Human Services - USA. The logo is a circular seal with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is an abstract symbol that resembles a stylized caduceus, with three human profiles facing to the right. The profiles are stacked on top of each other, creating a sense of depth and unity.

Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002

December 19, 2014

Varian Medical Systems, Inc. % Mr. Peter J. Coronado Director, Varian Oncology Systems Regulatory Affairs 911 Hansen Way PALO ALTO CA 94304

Re: K143224

Trade/Device Name: TrueBeam and Edge Radiotherapy Delivery System Regulation Number: 21 CFR 892.5050 Regulation Name: Medical charged-particle radiation therapy system Regulatory Class: II Product Code: IYE Dated: November 5, 2014 Received: November 10, 2014

Dear Mr. Coronado:

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. 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 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); 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.

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If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number [phone] or [phone] or at its Internet address

http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. 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 Industry and Consumer Education at its toll-free number [phone] or [phone] or at its Internet address

http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.

Sincerely yours,

Robert A. Ochs

Robert Ochs, Ph.D. Acting Director Division of Radiological Health Office of In Vitro Diagnostics and Radiological Health Center for Devices and Radiological Health

Enclosure

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#### DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration

## Indications for Use

510(k) Number (if known)

K143224

Device Name

TrueBeam and Edge Radiotherapy Delivery System

#### Indications for Use (Describe)

The TrueBeam and Edge Systems are intended to provide stereotactic radiosurgery for lesions, tumors, and conditions anywhere in the body where radiation therapy is indicated for adults and pediatric patients.

The TrueBeam and Edge Systems may be used in the delivery of radiation for treatment that includes: bram and spine tumors (such as glioma, meningioma, craniopharyngioma, pituitary tumors, spinal cord tumors, hemangioblastoma, orbital tumors, optic nerve tumors, and skull based tumors (such as unknown primary of the head and neck, oral cavity, hypopharynx, larynx, oropharynx, sinonasal, salivary gland, and thyroid cancer), thoracic tumors (such as ung cancer, esophageal cancer, thymic tumors, and mesothelioma), gynecologic tumors (such as ovarian, endometrial, vulvar, and vaginal), gastrointestinal tumors (such as gastric, hepatobiliary, colon, rectal, and anal carcinoma), genitourinary tumors (such as prostate, bladder, testicular, and kidney), breast tumors, sarcomas, lymphoid tumors (such as Hodgkin's lymphoma), skin cancers (such as squamous cell, and melanoma), benign diseases (such as schwannoma, arteriovenous malformation, cavemous malformation, trigeninal neuralgia, chordoma, glomus tumors, and hemangiomas), metastasis (including all parts of the body such as brain, bone, liver, lung, kidney, and skin) and pediatric tumors (such as glioma, pitutary tumors, hemangioblastoma, craniopharyngioma, metastasis, medulloblastoma, nasopharyngeal tumors, arteriovenous malformation, cavernous malformation and skull base tumors).

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)

## PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON A SEPARATE PAGE IF NEEDED.

### FOR FDA USE ONLY

Concurrence of Center for Devices and Radiological Health (CDRH) (Signature)

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# Premarket Notification [510(k)] Summary TrueBeam Radiotherapy Treatment System

The following information is provided following the format of 21 CFR 807.92.

| I. Submitter's Name: | Varian Medical Systems, Inc.<br>3120 Hansen Way C-260<br>Palo Alto, CA 94304<br><br>Contact Name: Peter J. Coronado<br>Phone: [phone]<br>Fax: [phone]<br>Date: November 2014 |
|----------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| II. Trade Name: | TrueBeamTM/TrueBeam STxTM/EdgeTM |
| Common Name: | Linear accelerator radiation therapy system |
| Classification Name: | Medical charged-particle radiation therapy system<br>21 CFR 892.5050, Class II<br>Product Code: 90 IYE |
| III. Predicate Device: | TrueBeam Radiotherapy System and Accessories: K140528 |
| IV. Device Description: | The TrueBeamTM Radiotherapy Delivery System is a medical linear<br>accelerator that integrates the previously cleared Trilogy Radiotherapy<br>system and associated accessories into a single device.<br><br>The system consists of two major components, a photon, electron, and<br>diagnostic kV X-ray radiation beam-producing component that is installed in<br>a radiation-shielded vault and a control console area located outside the<br>treatment room. |
| V. Intended Use<br>Statement | The TrueBeam TM system is intended to provide stereotactic radiosurgery and<br>precision radiotherapy for lesions, tumors, and conditions anywhere in the<br>body where radiation treatment is indicated. |
| Indications for Use<br>Statement | The TrueBeam and Edge Systems are intended to provide stereotactic<br>radiosurgery and precision radiotherapy for lesions, tumors, and conditions<br>anywhere in the body where radiation therapy is indicated for adults and<br>pediatric patients.<br><br>The TrueBeam and Edge Systems may be used in the delivery of radiation for<br>treatment that includes: brain and spine tumors (such as glioma, meningioma,<br>craniopharyngiaryngioma, pituitary tumors, spinal cord tumors, hemangioblastoma,<br>orbital tumors, ocular tumors, optic nerve tumors, and skull based tumors),<br>head and neck tumors (such as unknown primary of the head and neck, oral<br>cavity, hypopharynx, larynx, oropharynx, nasopharynx, sinonasal, salivary<br>gland, and thyroid cancer), thoracic tumors (such as lung cancer, esophageal<br>cancer, thymic tumors, and mesothelioma), gynecologic tumors (such as<br>ovarian, cervical, endometrial, vulvar, and vaginal), gastrointestinal tumors<br>(such as gastric, pancreatic, hepatobiliary, colon, rectal, and anal carcinoma),<br>genitourinary tumors (such as prostate, bladder, testicular, and kidney), breast<br>tumors, sarcomas, lymphoid tumors (such as Hodgkin's and non-Hodgkin's |

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lymphoma), skin cancers (such as squamous cell, basal cell, and melanoma), benign diseases (such as schwannoma, arteriovenous malformation, cavernous malformation, trigeminal neuralgia, chordoma, glomus tumors, and hemangiomas), metastasis (including all parts of the body such as brain, bone, liver, lung, kidney, and skin) and pediatric tumors (such as glioma, ependymoma, pituitary tumors, hemangioblastoma, craniopharyngioma, meningioma, metastasis, medulloblastoma, nasopharyngeal tumors, arteriovenous malformation, cavernous malformation and skull base tumors).

## VI. Technological Characteristics:

Significant changes to the predicate device are listed below.

| Feature | Cleared device | Device with change |
|---------------------------|----------------|--------------------|
| 80-leaf MLC | No | Yes |
| Manual bolus verification | No | Yes |

| VII. Summary of<br>performance<br>testing: | Hardware and software verification and validation testing was conducted<br>according to the FDA Quality System Regulation (21 CFR §820), ISO 13485 quality<br>Management System standard, ISO 14971 Risk Management Standard and the<br>other FDA recognized consensus standards listed below. Test results showed<br>conformance to applicable requirements specifications and assured hazard<br>safeguards functioned properly.<br>Software verification and validation testing were conducted and documentation<br>was provided as recommended by FDA's Guidance for Industry and FDA Staff,<br>"Guidance for the Content of Premarket Submissions for Software Contained in<br>Medical Devices." The software for this device was considered as a "major" level of<br>concern, since a failure or latent flaw in the software could directly result in serious<br>injury or death to the patient or operator.<br>The biocompatibility evaluation for the patient-contact materials in this medical<br>device was conducted in accordance with the FDA Blue Book Memorandum #G95-2<br>"Use of International Standard ISO-10993, 'Biological Evaluation of Medical Device<br>Part 1: Evaluation and Testing,'" May 1, 1995, and International Standard ISO<br>10993-1 "Biological Evaluation of Medical Devices – Part 1: Evaluation and Testing<br>Within a Risk Management Process," as recognized by FDA.<br>Electrical safety and electromagnetic compatibility (EMC) testing were conducted<br>on this medical device. The system complies with the IEC 60601-1 standards for<br>safety and the IEC 60601-1-2 standard for EMC. | | | | |
|--------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------|-----------------|--|--|
| Standards<br>conformance: | Varian TrueBeam™, TrueBeam STx™ and Edge™ medical linear accelerators<br>conform in whole or in part with the following FDA recognized consensus<br>standards: | | | | |
| | AAMI/ANSI/IEC 60601-1:2005 | IEC 60601-2-1: 2009 | IEC 61217: 2011 | | |
| | ANSI/AAMI/ISO 10993-1:2003 | IEC 60601-2-32: 1994 | IEC 62304: 2006 | | |
| | IEC 60601-1-2:2007 | IEC 60601-2-44: 2009 | IEC 62274: 2005 | | |
| | IEC 60601-1-3: 2008 | IEC 60825: 2007 | IEC 62366:2007 | | |
| | IEC 60601-1-6:2010 | IEC 60976: 2007 | | | |
| Conclusion: | The results of verification, validation and safety standards testing<br>demonstrate that the TrueBeam, TrueBeam STx, and Edge are substantially<br>equivalent to their predicate device | | | | |