Beamer AVEO Electrosurgical Generator, Beamer AVEO Argon Module, Beamer AVEO Cart, Beamer AVEO Wired Foot Pedal, Beamer AVEO Argon Pressure Reducer

Q: Who is the manufacturer of Beamer AVEO Electrosurgical Generator, Beamer AVEO Argon Module, Beamer AVEO Cart, Beamer AVEO Wired Foot Pedal, Beamer AVEO Argon Pressure Reducer?

Conmed Corporation filed the 510(k) submission for Beamer AVEO Electrosurgical Generator, Beamer AVEO Argon Module, Beamer AVEO Cart, Beamer AVEO Wired Foot Pedal, Beamer AVEO Argon Pressure Reducer (K214058).

Q: What is the FDA product code for Beamer AVEO Electrosurgical Generator, Beamer AVEO Argon Module, Beamer AVEO Cart, Beamer AVEO Wired Foot Pedal, Beamer AVEO Argon Pressure Reducer?

GEI. It is classified under 21 CFR 878.4400 as a Class 2 device in the General, Plastic Surgery panel.

Q: What is the regulatory pathway for Beamer AVEO Electrosurgical Generator, Beamer AVEO Argon Module, Beamer AVEO Cart, Beamer AVEO Wired Foot Pedal, Beamer AVEO Argon Pressure Reducer?

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

Q: Who can help prepare an FDA 510(k) submission like Beamer AVEO Electrosurgical Generator, Beamer AVEO Argon Module, Beamer AVEO Cart, Beamer AVEO Wired Foot Pedal, Beamer AVEO Argon Pressure Reducer?

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.

K214058 · Conmed Corporation · GEI · Aug 26, 2022 · General, Plastic Surgery

Device Facts

Record ID	K214058
Device Name	Beamer AVEO Electrosurgical Generator, Beamer AVEO Argon Module, Beamer AVEO Cart, Beamer AVEO Wired Foot Pedal, Beamer AVEO Argon Pressure Reducer
Applicant	Conmed Corporation
Product Code	GEI · General, Plastic Surgery
Decision Date	Aug 26, 2022
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 878.4400
Device Class	Class 2
Attributes	Therapeutic

Intended Use

The Beamer AVEO™ Electrosurgical Generator System with Accessories is intended to deliver electrosurgical current and Argon gas for the cutting, coagulation and argon beam assisted coagulation of tissue. The Beamer AVEO™ System is used in conjunction with compatible applicators or probes.

Device Story

Electrosurgical generator system delivering high-frequency (HF) current and Argon gas for tissue cutting and coagulation. System comprises generator (AVEO-ESU), Argon module (AVEO-ABC), cart, wired foot pedal, and pressure reducer. Operated by clinicians in surgical settings. User interacts via 7-inch touchscreen GUI and footswitches to select programs, modes, power settings, and Argon flow rates. Device monitors neutral electrode status and contact quality. Output delivered through compatible monopolar/bipolar instruments and Argon probes. Provides enhanced bleeding control via Argon beam. Benefits include precise tissue management during surgical procedures.

Clinical Evidence

Bench testing only. Thermal effects on tissue (liver, muscle, kidney) evaluated in triplicate at min/default/max settings per FDA guidance. Electrical safety and electromagnetic compatibility testing performed per IEC 60601-1, IEC 60601-1-2, and IEC 60601-2-2. Risk management conducted per ISO 14971.

Technological Characteristics

High-frequency electrosurgical generator with integrated Argon module. 7" touchscreen LCD interface. Connectivity for monopolar (4mm), bipolar (coaxial), and Argon probes. Duty cycle: 10s/30s. Compliance: IEC 60601-1 (Ed 3.1), IEC 60601-1-2 (Ed 4.0), IEC 60601-2-2 (Ed 6.0).

Indications for Use

Indicated for all patient types and conditions where electrosurgery is relevant, on all parts of the human body, for cutting, coagulation, and argon beam assisted coagulation of tissue.

Regulatory Classification

Identification

An electrosurgical cutting and coagulation device and accessories is a device intended to remove tissue and control bleeding by use of high-frequency electrical current.

Predicate Devices

VIO 300D (K083452)

Reference Devices

ConMed Beamer System (K081678)
ERBE APC 2 (K024047)

Related Devices

K172671 — HelixAR Electrosurgical Generator with Argon Beam Coagulation, HelixAR Mobile Pedestal · Conmed Corporation · Oct 4, 2017
K180200 — ESG-300, APU-300, Pressure Reducer, MAPC Probes · Olympus Winter & Ibe GmbH · Apr 26, 2018
K203522 — Surn5 Electrosurgical Argon Beam Generator and Accessories · Surnic Corporation · Feb 22, 2021
K152860 — HELIXAR ELECTROSURGICAL GENERATOR WITH ARGON BEAM COAGULATION, HELIXAR MOBILE PEDESTAL · Conmed Corporation · Dec 29, 2015
K100669 — CANADY PLASMA ELECTROSURGICAL UNIT SERIES WITH ACCESSORY PROBES AND BLADES · Us Medical Innovations, LLC · Apr 6, 2011

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image contains two logos. The logo on the left is the Department of Health & Human Services logo. The logo on the right is the FDA logo, which stands for U.S. Food & Drug Administration. The FDA logo is in blue. August 26, 2022 ConMed Corporation Ms. Kavita Amin, MSRA Sr. Specialist, Regulatory Affairs 525 French Road Utica, New York 13502 Re: K214058 Trade/Device Name: Beamer AVEO Electrosurgical Generator, Beamer AVEO Argon Module Regulation Number: 21 CFR 878.4400 Regulation Name: Electrosurgical cutting and coagulation device and accessories Regulatory Class: Class II Product Code: GEI Dated: June 29, 2021 Received: July 1, 2022 Dear Ms. Amin: 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 medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-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, for Long Chen, Ph.D. Assistant Director DHT4A: Division of General Surgery Devices OHT4: Office of Surgical and Infection Control Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ ## Indications for Use 510(k) Number (if known) K214058 #### Device Name Beamer AVEO Electrosurgical Generator and Argon Module Indications for Use (Describe) The Beamer AVEO™ Electrosurgical Generator System with Accessories is intended to deliver electrosurgical current and Argon gas for the cutting, coagulation and argon beam assisted coagulation of tissue. The Beamer AVEO™ System is used in conjunction with compatible applicators or probes. | Type of Use (Select one or both, as applicable) | | |-------------------------------------------------------------------------------|------------------------------------------------------------------------------| | <div> Prescription Use (Part 21 CFR 801 Subpart D) </div> | <div> Over-The-Counter Use (21 CFR 801 Subpart C) </div> | #### 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}------------------------------------------------ # 510(k) SUMMARY Beamer AVEO™ Electrosurgical Generator and Argon Module #### Submitter Name and Address: ConMed Corporation 525 French Road Utica, NY -13502 USA ### Contact Person Name and Telephone: Ms. Kavita Amin, MSRA Sr Specialist, Regulatory Affairs ConMed Advanced Endoscopic Technologies 525 French Road Utica, NY-13502 Telephone: 508-948-2084 Email address: kavitaamin@conmed.com ### Date of Summary Prepared: August 23, 2022 #### Name of the device: | Trade Name: | Beamer AVEO™ | |----------------------|----------------------------------------------------------------------| | Device Name: | Beamer AVEO™ Electrosurgical Generator; Beamer AVEO™ Argon Module | | Common Name: | Beamer AVEO™ System, AVEO System | | Classification Name: | Class II | | Product Code: | GEI | #### Predicate Device: The information presented in this submission demonstrates the Beamer AVEO™ Electrosurgical Generator and Argon Module is substantially equivalent in function to its predicate device, VIO 300D, and reference device, ConMed Beamer System . The list of predicate and reference devices are provided in Table 1 below. | 510(k) Number | Product Code | Trade Name | Manufacturer | | |---------------------|-----------------|------------|----------------------|------------| | Predicate Device | K083452 | GEI | VIO 300D | Erbe | | Reference Device | K081678 | GEI | ConMed Beamer System | KLS Martin | #### Table 1: List of Predicate and Reference Devices {4}------------------------------------------------ #### Device Description: The Beamer AVEO™ Electrosurgical Generator and Argon Module (aka Beamer AVEO System / Beamer AVEO Electrosurgical System) is an electrosurgical generator that is used in surgical procedures and uses High-Frequency (HF) current through an accessory electrode for cutting and coagulation at the operative site. It is also intended to be used for enhanced control of bleeding by the delivery of HF electrosurgical current in combination with Argon gas through a compatible accessory. The Beamer AVEO System can be used for all patient types, conditions where electrosurgery is relevant, on all parts of human body. The Beamer AVEO System is comprised of an Electrosurgical Generator (AVEO-ESU), Argon Module control (AVEO-ABC), Beamer AVEO cart and accessories (wired foot pedal, pressure reducer). A Graphical User Interface (GUI) and associated footswitches are provided for user interaction. Monopolar instruments, bipolar instruments, Argon probes, and a footswitch are connected to the AVEO system. #### Indications for Use: The Beamer AVEO™ Electrosurgical Generator System with Accessories is intended to deliver electrosurgical current and Argon gas for the cutting, coagulation and argon beam assisted coagulation of tissue. The Beamer AVEO™ System is used in conjunction with compatible applicators or probes. #### Summary of Technological Characteristics: The subject device is similar in design as the predicate and reference devices. The subject device has the same intended use as the predicate and reference devices. The Beamer AVEO System is comprised of an electrosurgical unit and argon unit as the predicate device. All three systems use same technology of high frequency energy for cutting and coagulation of tissue. #### Substantial Equivalence: Table 2 provides the similarities and differences between the predicate and reference devices. The modifications made to the subject device do not raise any risk to safety or effectiveness. Supporting information per this premarket submission confirms that the Beamer AVEO Electrosurgical Generator is safe and effective for its intended use and is substantially equivalent in design, intended use, principals of operation, and technical characteristics to the predicate and reference devices. | Features | Subject Device: Beamer AVEO System | Predicate Device: ERBE VIO 300 D / ERBE APC 2 | Reference Device: ConMed Beamer System CE600 | |---------------------------------|--------------------------------------------------------------------------|-----------------------------------------------------|----------------------------------------------------| | 510(k) | K214058 | K083452 / K024047 | K081678 | | Duty Cycle | Non-continuous 10 seconds/ 30 seconds | Non-continuous 10 seconds/ 30 seconds | Non-continuous 10 seconds/ 30 seconds | | Energy Type | High Frequency (HF), Argon | High Frequency (HF), Argon | High Frequency (HF), Argon | | Output | Monopolar, Bipolar, Argon | Monopolar, Bipolar, Argon | Monopolar, Bipolar, Argon | | Electrical Safety Compliance | IEC 60601-1, Ed. 3.1 IEC 60601-1-2, Ed. 4.0 IEC 60601-2-2, Ed. 6.0 | IEC 60601-1 IEC 60601-1-2 IEC 60601-2-2 | IEC 60601-1 IEC 60601-1-2 IEC 60601-2-2 | | Table 2: Substantial Equivalence | | | | | | |----------------------------------|--|--|--|--|--| |----------------------------------|--|--|--|--|--| {5}------------------------------------------------ | Features | Subject Device: Beamer AVEO System | Predicate Device: ERBE VIO 300 D / ERBE APC 2 | Reference Device: ConMed Beamer System CE600 | |---------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Display | The Beamer AVEO ESU is designed with a 7" touch screen LCD display. The screen displays program, mode, power settings, argon flow rate, argon tank status, neutral electrode status and contact quality (dual-foil electrodes), user programs, and visual indications. | The VIO 300 D is designed with a backlit dual color screen controlled via selection buttons located on either side of the screen. The screen displays program, mode, power settings, | The ConMed Beamer System CE600 is designed with an 8" screen containing push buttons and rotary switch (knob) for navigation. The screen displays program, mode, power settings, argon flow rate, argon tank status, neutral electrode status and contact quality (dual- foil electrodes), user programs, and visual indications. | | Foot Pedal Connections | Accommodates the following foot pedal connections: Dual | Accommodates the following foot pedal connections: – Dual Single | Accommodates the following foot pedal connections: – Dual – Single | | Purge | The Beamer AVEO System provides a purge function of 3 LPM ± 20% for 4 seconds. | The VIO 300 D with connected APC 2 module provides a 3-second purge with flow rate dependent upon the type of instrument connected to the APC 2. | The Beamer System CE600 provides a purge function of 3 LPM ± 20% for 3 seconds. | | Modes | The Display screen has indicators / icons to identify the selected program, power settings for each mode, instrument used and the selected argon gas flow rate. | The Display screen has indicators / icons to identify the selected program, power settings for each mode, and the selected argon gas flow rate. | The Display screen has indicators / icons to identify the selected program, power settings for each mode and the selected argon gas flow rate. | | Programmable settings | The Beamer AVEO System is designed to allow users to create, recall, modify, and delete user-defined programs. | The VIO 300 D is designed to allow users to create, recall, modify, and delete user- defined programs. | The Beamer System CE600 is designed to allow users to create, recall, modify, and delete user-defined programs. | | Features | Subject Device: Beamer AVEO System | Predicate Device: ERBE VIO 300 D / ERBE APC 2 | Reference Device: ConMed Beamer System CE600 | | Instrument Connections | The Beamer AVEO System accommodates the following instrument connections: – Monopolar (Bovie- type, 3-prong, 4mm) – Bipolar (coaxial, 2- prong) – Argon (ConMed proprietary design) | The ERBE VIO 300 D accommodates the following instrument connections: – Monopolar – Bipolar Argon (via APC Module) | The ConMed Beamer System CE600 accommodates the following instrument connections: – Monopolar (Bovie- type, 3-prong, 4mm) – Bipolar (coaxial, 2- prong) – Argon (Luer connection) | {6}------------------------------------------------ #### Performance Testing: Performance testing demonstrates that the Beamer AVEO System is substantially equivalent to the predicate device with regard to its intended use, materials, technology, and performance. Testing demonstrates the devices comply with the applicable sections of AAMI/ANSI ES60601-1, IEC 60601-2-2, and IEC 60601-1-2. Risk management activities in accordance with ISO 14971 demonstrate the risks associated with the use of the Beamer AVEO system are mitigated to an acceptable level. Analyses of these activities conclude the benefits associated with the use of the Beamer AVEO System outweigh the residual risks. Thermal Effects on Tissue testing was conducted on Beamer AVEO™ Electrosurgical Generator and Argon Module per FDA Guidance, "Premarket Notification (510(k)) Submissions for Electrosurgical Devices for General Surgery". The test was conducted on three different tissues (Liver, Muscle and Kidney) in triplicate at the minimum, default and maximum settings. The test results and analysis showed that the thermal effects on tissues of the Beamer AVEO™ Electrosurgical Generator and Argon Module are substantially equivalent to the predicate and reference devices. All test results were acceptable. #### Conclusion: The subject device is substantially equivalent to the commercially available marketed device, ConMed Beamer System and Erbe VIO 300D. The modifications expressed in this 510(k) Premarket Notification do not change the intended use, nor alter the fundamental scientific technology of the device, and do not raise any new issues of safety and effectiveness.