CERTUS 140 CERTUSURGGT SURGICAL TOOL

{0}------------------------------------------------ K130399 Page 1 of 3 | JUL | 1 | 8 | 2013 | |-----|---|---|------| |-----|---|---|------| | Date: | 02/15/2013 | |--------------------|---------------------------------------------------------------------| | Subject: | 510(k) Summary of Safety and Effectiveness Information for the | | | NeuWave Medical Certus 140 2.45 GHz Ablation System and Accessories | | Company: | NeuWave Medical, Inc. | | | 3529 Anderson Street | | | Madison, WI 53704 | | FDA Establishment# | 3008769756 | | Contact: | Dan Kosednar, Director of Regulatory Affairs and Quality Assurance | | | P - 608-512-1592 | | | F - 608-512-1509 | | Proprietary: | Certus 140 2.45 GHz Ablation System and Accessories | | Common: | System, Ablation, Microwave and Accessories | | Classification: | Surgical Devices, 73 NEY, 21 CFR 878.4440 | The 510(k) summary of safety and effectiveness information is being submitted in accordance with the requirements of SMDA 1990 and 1992. #### Predicate Devices The Certus 140 2.45 GHz Ablation System and Accessories is substantially equivalent to the following currently marketed device: - Certus 140 2.45 GHz Ablation System and Accessories Class II 21CFG878.4400 which . has been the subject of a cleared 510(k) with the FDA log number K100744, K113237 and K122217. #### Indications For Use The NeuWave Medical Certus 140™ 2.45 GHz Ablation System and Accessories are indicated for the ablation (coagulation) of soft tissue in percutaneous, open surgical and in conjunction with laparoscopic surgical settings. The Certus 140™ 2.45 GHz Ablation System is not indicated for use in cardiac procedures. The system is designed for facility use and should only be used under the orders of a clinician. #### Device Description The system has a single 2.45 GHz signal source generator and three (3) independent power amplifiers, each capable of producing up to 140W each. One, easy to use, touch-screen user interface controls the system. The User Interface can be set for either Ablation Mode or Surgical Mode. An optional footswitch can be connected to the system to control power delivery in Surgical Mode. Up to three (3) energy delivery accessories can be connected to and powered by the system at one time. An intermediate junction box or Power Distribution Module (PDM) reduces system set up complexity. Certus 140 510(k) Submission Safety Summary Page 1 of 3 {1}------------------------------------------------ A variety of sterile, single-patient use energy delivery accessories (ablation probes and surgical tools) are available for use with the Certus 140. All are comprised of a sharp trocar on the end of a cannula, a handle, a cable and a connector assembly. Models Certus™, Certus ", and Certus " ablation probes have 17 gauge cannulas and are available in 15 cm and 20 cm lengths. These probes have a cable length of 1.4m. The model Certus® ablation probe has a 13 gauge cannula and is available in a 25 cm length only. Certus 6 probes have a cable length of 1.4m. CertuSurg" surgical tool is hand-held and has a 6cm, 17 gauge cannula designed specifically for surgical coagulation (including Planar Coagulation) in open surgical settings. This device has a finger-activated power delivery mechanism and a cable length of 2.9m. | | Percutaneous<br>Ablation | Laparoscopic<br>Ablation | Open Surgical<br>Ablation | Open Surgical<br>Coagulation | |-------------|--------------------------|--------------------------|---------------------------|------------------------------| | CertusLK | X | | X | X | | CertusLN | X | | X | | | CertusPR | X | | X | X | | CertusSR | | X | X | | | CertuSurgGT | | | X | | Ablation Probe/Surgical Tool Design Application Overview * The CertuSurgGT is not recommended for Target Ablation procedures lasting more than 1 minute. Each energy delivery accessory contains temperature measurement sensors that help monitor performance and ensure patient and operator safety. Additionally, the different percutaneous ablation probes have been designed to optimize the energy transfer efficiency from the probe into different types of tissue based on known electrical properties of each tissue. Certus " probes are designed to perform optimally, in terms of efficiently transferring energy into tissue, in liver and kidney tissue. Certus " probes are designed to perform optimally, in terms of efficiently transferring energy into tissue, in lung tissue. The antenna of the Certus " probe is designed to limit the length of the ablation for instances when a shorter ablation zone is desired. Certus " Probes were developed to provide physicians with an additional ablation probe designed specifically for ablating smaller lesions. The Certus® probes are designed to produce ablations that quickly encompass the tip of the probe while limiting the overall length of the ablation. Certus® probes will enable physicians to ablate smaller lesions while limiting necrosis of adjacent tissue when compared to other Certus probes. The Certus \$ probes length and gauge size result in a sturdy probe ideal for use in laparoscopic applications. The CertuSurg " surgical tool is designed to produce focal, rapid coagulation of soft tissue in open surgical applications, including planar coagulation performed prior to tissue resection. {2}------------------------------------------------ A CO2 based cooling system ensures the non-active portion of the probe does not exceed temperature requirements. Additionally, the CO2 enables the Tissu-Loc function, which can be used to adhere or stick the probe in place prior to starting ablation therapy. This function is similar in use to the stick function available on cryogenic ablation systems. CertuSurg" surgical tool does not have the Tissu-Loc function. The system uses two (2) E-sized CO2 cylinders. When a tank in use empties, the system will automatically switch to using the other tank and notify the user to replace the empty tank. ### Modifications This 510(k) was submitted to update the Certus 140 system with: - The new CertuSurgST surgical tool. . - Software updates associated with the use of the CertuSurg® surgical tool. . #### Performance Data The Certus 140 2.45 GHz Ablation System and Accessories has been designed to comply with the applicable portions of various International Standards, including: - . UL 60601-1:2003 - IEC 60601-1:1988 Plus Amendments . - IEC 60601-2-2:2006 . - . IEC 60601-2-6:1984 - . IEC 60601-1-2:2007 - . EN ISO 11607-1:2009 - ISO 10993-1: 2009 ● The Certus 140 2.45 GHz Ablation System and Accessories and the predicate devices are substantially equivalent in design concepts, technologies and materials. The Certus 140 Ablation 2.45 GHz System and Accessories has been verified through rigorous testing that, in part, supports the compliance of Certus 140 2.45 GHz Ablation System and Accessories to the standards listed above. Ex-vivo studies were conducted to compare the performance of the Certus 140 2.45 GHz Ablation System and Accessories to a predicate device. {3}------------------------------------------------ Image /page/3/Picture/0 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo features a stylized eagle with three lines representing its body and wings. The eagle is enclosed in a circle, and the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is written around the circle. ### DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-002 July 18, 2013 Neu Wave Medical, Inc. % Dan Kosednar, RAC Director, Regulatory Affairs and Quality Assurance 3529 Anderson Street Madison, Wisconsin 53704 Re: K130399 Trade/Device Name: Certus 140 2.45GHz Ablation System and Accessories Regulation Number: 21 CFR 878.4400 Regulation Name: Electrosurgical cutting and coagulation device and accessories Regulatory Class: Class II Product Code: NEY Dated: June 18, 2013 Received: June 20, 2013 Dear Mr. Kosednar: 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 mav 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 {4}------------------------------------------------ Page 2 - Dan Kosednar, RAC 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. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR 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/MedicalDevices/Resourcesfor You/Industry/default.htm. Sincerely yours, ## Mark N. Melkerson -S Mark N. Melkerson Acting Director Division of Surgical Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {5}------------------------------------------------ # Indications for Use 510(k) Number (if known): K Device Name: Certus 140 2.45GHz Ablation System and Accessories Indications For Use: The NeuWave Medical Certus 140™ 2.45 GHz Ablation System and Accessories are indicated for the ablation (coagulation) of soft tissue in percutaneous, open surgical and in conjunction with laparoscopic surgical settings. The Certus 140™ 2.45 GHz Ablation System is not indicated for use in cardiac procedures. The system is designed for facility use and should only be used under the orders of a clinician. Prescription Use XXX (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use (21 CFR 807 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Page 1 of 1 | DSD-DIVISION SIGN-OFF | Joshua C. Nipper | |------------------------------|------------------| | Division of Surgical Devices | | | 510(k) Number: | K130399 |