LIGHTWAVE INTEGRATED ELECTRODE ABLATOR AND LIGHT WAVE INTEGRATED ELECTRODE SUCTION ABLATOR

{0}------------------------------------------------ Page 1 of (3) April 5, 2005 ## 510(k) Submission Summary of Safety and Effectiveness In accordance with the requirements of the Safe Medical Device Act of 1990 and 21 CFR 807.92, ConMed/Linvatec is hereby submitting a 510(k) Summary of Safety and Effectiveness for the LightWave™ Integrated Electrode Ablator and LightWave™ Integrated Electrode Suction Ablator 510(k) # KO50923 #### A. Submitter ConMed/Linvatec 11311 Concept Boulevard Largo, Florida 33773-4908 #### B. Company Contact Elizabeth Paul Manager, Regulatory Affairs (727) 399-5234 Telephone (727) 399-5264 FAX #### C. Device Name Trade Name: LightWave Integrated Electrode Ablator and LightWave Integrated Electrode Suction Ablator Common Name: Electrode Classification Names: Electrosurgical cutting and coagulation device and accessories, CFR 878.4400 Proposed Class/Device: Class II Product Code: JOS & GEI {1}------------------------------------------------ Page 2 of 3 Summary of Safety and Effectiveness LightWave" Integrated Electrode Ablator and LightWave" Integrated Electrode Suction Ablator 510(k) #_ KO50923 April 5, 2005 Page 2 of 3 - #### Predicate/Legally Marketed Devices D. - K993885 UltrAblator, Linvatec Corporation - K002422 VAPR™ 3.5mm 90° Suction Electrode for use with the VAPR™ System, Mitek Products - K021299 Heatwave Hand-Controlled Electrode, ConMed Corporation K030720 - UltrAblator, Linvatec Corporation K983652 - Linvatec Switch Pencil, Linvatec Corporation #### Device Description E. The ConMed/Linvatec LightWave" Integrated Electrode Ablators are a modification of the currently marketed 3.2 mm UltrAblator electrode (Linvatec, K030720) and a Switch Pencil control handle (Linvatec, K983652) integrated into one device. One version incorporates handcontrolled buttons to actuate the "cut" and "coag" functions of the electrosurgical generator. Another version is actuated by foot-control to control "cut" and "coag" functions of the electrosurgical generator. The hand-controlled and foot controlled version consists of an electrical insulation coated electrode and ceramic insulator attached to an integrated handle and cord set, allowing attachment to commonly available electrosurgical generators in distribution. A third version of the ConMedILinvatec LightWave™ Integrated Electrode Ablators incorporates a suction/aspiration feature and is a modification of the currently marketed 3.2 mm Ult Ablator electrode (Linvatec, K993885) and a Switch Pencil control handle (Linvatec, K983652) integrated into one device, and is similar in technology to Heatwave Hand-Controlled Electrode (Conmed, K021299) and the VAPR™ 3.5mm 90° Suction Electrode (Mitek, K002422), which incorporate aspiration or suction. The device is similar to the hand-controlled device and will also have suction capability and attach to commonly available suction equipment. This electrode will be hollow allowing for the removal of irrigating fluids during surgical procedures. {2}------------------------------------------------ Page 3 of 3 Summary of Safety and Effectiveness LightWave™ Integrated Electrode Ablator and LightWave™ Integrated Electrode Suction Ablator 510(k) #_ KOSO923 April 5, 2005 Page 3 of 3 The front switch contained in the hand-controlled devices provide the surgeon with electrosurgical cut (ablate) capability when depressed. The rear button activates electrosurgical coagulating (coag) current. #### Intended Use F. The ConMed/Linvatec LightWave™ Integrated Electrode Ablators are intended to be used for electrosurgical cutting and coagulation in shoulder, ankle, wrist, elbow, and knee arthroscopic procedures in a conductive fluid environment. Additionally, the suction/aspiration version also has capability for suctioning irrigation fluids. #### Substantial Equivalence G. The ConMed/Linvatec LightWave™ Integrated Electrode Ablators are substantially equivalent to the dentified predicate devices below in intended use and surgical effect, function, materials of construction, patient population, compliance with recognized standards and published FDA guidance for devices of this type, and manufacturing methods. The predicate devices are intended for use in conjunction with an electrosurgical generator controlled by hand or footswitch for use during arthroscopic procedures. Either hand control or foot switch control are used to control the duration of electrosurgical current delivered to the operative site via the electrode. The ConMed/Linvatec LightWave" Integrated Electrode Ablators are a one-piece design that incorporates the functions of the Linvatec brand predicate devices, as well as similar performance and technological characteristics of the other predicate devices, into one ergonomic handle and electrode combination. Differences exist between the predicates and new device in that one version of the new device offers a suction feature through the electrode center with maximum cut power of 200 watts. A comparison table of the currently marketed devices and the device subject to this application submission is attached. ## Substantially Equivalent Predicate Marketed Devices: - K993885 UltrAblator, Linvatec Corporation - K002422 VAPRTM 3.5mm 90° Suction Electrode for use with the VAPR™ System, Mitek Products - K021299 Heatwave Hand-Controlled Electrode, Conmed Corporation - K030720 UltrAblator, Linvatec Corporation - K983652 Linvatec Switch Pencil, Linvatec Corporation {3}------------------------------------------------ DEPARTMENT OF HEALTH & HUMAN SERVICES Image /page/3/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo consists of a stylized eagle with three curved lines representing its body and wings. The text "DEPARTMENT OF HEALTH AND HUMAN SERVICES. USA" is arranged in a circular pattern around the eagle. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 MAY 1 8 2005 Ms. Elizabeth M. Paul Manager, Regulatory Affairs Linvatec Corporation 11311 Concept Boulevard Largo, Florida 33773-4908 Re: K050923 Trade/Device Name: LightWave™ Integrated Electrode Ablator and LightWave™ Integrated Electrode Suction Ablator Regulation Number: 21 CFR 878.4400 Regulation Name: Electrosurgical cutting and coagulation device and accessories Regulatory Class: II Product Code: JOS & GEI Dated: April 11, 2005 Received: April 13, 2005 Dear Ms. Paul: 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 (PMA), 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. 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 sct 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. {4}------------------------------------------------ Page 2 - Ms. Elizabeth M. Paul This letter will allow you to begin marketing your device as described in your Section 510(k) I mis letter will and in yours of substantial equivalence of your device to a legally premation nourseanon " 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 If you desire specific aarnoliance at (240) 276-0115 . Also, please note the regulation entitled, Connect the Oriece of Comphalled as (21 transmit (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small other general micronal and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html. Sincerely yours, Miriam C. Provost, Ph.D. Acting Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {5}------------------------------------------------ # Indications for Use 510(k) Number (if known):_____________________________________________________________________________________________________________________________________________________ Device Name: LightWave™ Integrated Electrode Ablator and LightWave™ Integrated Electrode Suction Ablator ### Indications for Use: The ConMed/Linvatec LightWave™ Integrated Electrode Ablators are intended to be used for electrosurgical cutting and coagulation in shoulder, ankle, wrist, elbow, and knee arthroscopic procedures in a conductive fluid environment. Additionally, the suction/aspiration version also has capability for suctioning irrigation fluids. OR Prescription Use_X_ (Part 21 CFR 801 subpart D) Over-the-Counter Use · (Part 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 Page 1 of __ 1 Restorative Devices