VAPR VUE RADIOFREQUENCY SYSTEM ,MODEL 225024, VPR VUE WIRELESS FOOTSWITCH, MODEL 227214
Device Facts
| Record ID | K100638 |
|---|---|
| Device Name | VAPR VUE RADIOFREQUENCY SYSTEM ,MODEL 225024, VPR VUE WIRELESS FOOTSWITCH, MODEL 227214 |
| Applicant | Depuy Mitek, A Johnson & Johnson Company |
| Product Code | GEI · General, Plastic Surgery |
| Decision Date | Jun 18, 2010 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 878.4400 |
| Device Class | Class 2 |
| Attributes | Therapeutic |
Indications for Use
The Mitek VAPR VUE Radiofrequency System is intended for resection, ablation and excision of soft tissue, hemostasis of blood vessels and coagulation of soft tissues in patients requiring arthroscopic surgery of the knee, shoulder, ankle, elbow and wrist. The DePuy Mitek VAPR Electrodes for use with the VAPR VUE Radiofrequency System are intended for resection, ablation and excision of soft tissue, hemostasis of blood vessels and coagulation of soft tissue in patients requiring arthroscopic surgery of the knee, shoulder, ankle, elbow, and wrist.
Device Story
VAPR VUE Radiofrequency System is an electrosurgical generator with wired/wireless footswitch and electrodes; utilizes bipolar RF technology for arthroscopic soft tissue ablation, contouring, cutting, and coagulation. System inputs include user-selected modes (Vaporization, Coagulation, CP Vaporization, Blended Vaporization, temperature control) via footswitch or handcontrols. Electrodes (P50, P90, CP90) perform tissue interaction; suction electrodes remove bubbles from operating site. Used in OR by surgeons during arthroscopic procedures. Output provides RF energy to tissue; handcontrols on CP90 allow surgeon to adjust ablation/coagulation modes directly. System benefits include precise tissue management and improved visualization via bubble removal. Enhancements over legacy VAPR3 include CP output type and expanded peak power range.
Clinical Evidence
No clinical studies were required. Substantial equivalence is supported by bench testing, including electrical safety, electromagnetic compatibility, and software validation performed in accordance with EN 60601-1, EN 60601-2-2, EN 60601-1-2, and ISO 62304 standards.
Technological Characteristics
Bipolar electrosurgical system; generator-based RF energy delivery. Components: generator, wired/wireless footswitch, electrodes (P50, P90, CP90). Features: suction capability for bubble removal, handcontrol integration. Connectivity: wireless footswitch. Software: programmable electrical medical system. Standards: EN 60601-1, EN 60601-2-2, EN 60601-1-2, ISO 60601-1-4, ISO 62304.
Indications for Use
Indicated for resection, ablation, excision of soft tissue, and hemostasis of blood vessels in patients requiring arthroscopic surgery of the knee, shoulder, ankle, elbow, and wrist.
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
- VAPRIII (K041135)
- Gyrus SuperPulse Electrosurgical Generator (K031085)
- ConMed Linvatec Zen Wireless Footswitch (K083161)
- Linemaster IR Wireless Footswitch System (K053510)
- Stryker Wireless Universal Footswitch (K033135)
- VAPR 90° Suction Electrode (K002422)
- VAPR LPS Electrode (K041135)
- VAPR Electrodes with Handpieces (K082643)
- 2.3 Wedge Effect Electrode (K992876)
Submission Summary (Full Text)
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KC100638
JUN 1 8 2010
## 510(k) SUMMARY
Date Prepared March 4, 2010 Submitter's Name and DePuy Mitek, Inc. Address: a Johnson & Johnson company 325 Paramount Drive · Raynham, MA 02767 Contact Person Susan Kagan Project Manager, Regulatory Affairs DePuy Mitek, Inc. a Johnson & Johnson company 325 Paramount Drive Raynham, MA 02767, USA Telephone: 508-880-8097 Facsimile: 508-977-6955 e-mail: skagan@its.jnj.com Name of Medical Classification Name: Electrosurgical cutting and coagulation device Device and accessories: 21 CFR 878.4400 Electrosurgical cutting and coagulation device Common/Usual Name: and accessories: Arthroscope VAPR® VUE™ Radiofrequency System Proprietary Name: P50 Electrode P90 Electrode CP90 Electrode CP90 Electrode with Handcontrol FDA Classification: ll FDA product code: GEI The proposed VAPR VUE Radiofrequency System is substantially Predicate Device(s) equivalent to: K041135: VAPRIIITM (May 10, 2004) 트 The proposed VAPR VUE Radiofrequency System is also similar to: K031085: Gyrus SuperPulse Electrosurgical Generator (July 21, I 2003)
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| | The proposed Wireless Footswitch is substantially equivalent to: |
|--------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| | K083161: ConMed Linvatc Zen Wireless Footswitch K053510: Linemaster IR Wireless Footswitch System K033135: Stryker Wireless Universal Footswitch |
| | The proposed P90 and CP90 Electrodes are substantially equivalent to: |
| | K002422: VAPR 90° Suction Electrode (August 31, 2000) K041135: VAPR LPS Electrode (May 10, 2004) K082643: VAPR Electrodes with Handpieces (December 19, 2008) |
| | The proposed P50 Electrode is substantially equivalent to: |
| | K992876: The 2.3 Wedge Effect Electrode (September 24, 1999) K041135: VAPR LPS Electrode (May 10, 2004) K082643: VAPR Electrodes with Handpieces (December 19, 2008) |
| Device Description | The VAPR VUE Radiofrequency System is DePuy Mitek's next generation<br>of VAPR Radiofrequency Systems. The system consists of a generator,<br>wired or wireless footswitch and electrodes. The VAPR VUE generator<br>was designed to provide comparable RF performance with legacy VAPR<br>electrodes. |
| | As with its predicate devices including the VAPR 3 generator, this<br>electrosurgical system utilizes bipolar technology specifically designed to<br>provide a range of arthroscopic surgical treatments including soft tissue<br>ablation, contouring, cutting and coagulation and temperature control. |
| | The VAPR VUE system offers five output types of operation: Vaporization<br>(ablation), Coagulation, CP Vaporization (ablation), Blended Vaporization<br>(ablation and coagulation) and temperature control coagulation. All<br>types are present in the predicate device (VAPR3 generator) except the<br>CP Vaporization (ablation). |
| | The VAPR P50 and P90 Electrodes are an addition to the family of LPS<br>Electrodes. These Suction Electrodes are soft tissue ablation and<br>coagulation devices intended for use with the VAPR Electrosurgical<br>Systems. They extend the utility of the system by removing bubbles<br>created during activation from the operating site. |
| | The VAPR CP90 Electrodes are identical in technological characteristics<br>as the P90 electrode only it is intended to be run only off the VAPR VUE<br>platform at pre-determined default settings specific for the device. The<br>CP90 with Handcontrols offers the integration of handcontrol capabilities<br>via three buttons molded on the existing one-piece handles. Those |
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buttons control ablation, coagulation and the generator mode functions.
#### Indications for Use
The Mitek VAPR VUE Radiofrequency System is intended for resection, ablation and excision of soft tissue, and hemostasis of blood vessels in patients requiring arthroscopic surgery of the knee, shoulder, ankle, elbow and wrist.
The P50 and P90 Electrodes when used with Mitek VAPR Electrosurgical Systems are intended for resection, ablation and excision of soft tissue, and hemostasis of blood vessels in patients requiring arthroscopic surgery of the knee, shoulder, ankle, elbow and wrist.
The VAPR CP90 Electrodes when used with Mitek VAPR VUE Electrosurgical System is intended for resection, ablation and excision of soft tissue, and hemostasis of blood vessels in patients requiring arthroscopic surgery of the knee, shoulder, ankle, elbow and wrist.
### Comparison to Predicate Device
This submission is intended to demonstrate that the VAPR VUE Radiofrequency System, P50, P90 and CP90 Electrodes are substantially equivalent to their legally marketed devices.
The Electrodes have been carefully compared to legally marketed devices with respect to intended use, essential components and material, performance specifications and technology characteristics. All of the electrodes which are the subject of this submission have the same Indications for Use and technology characteristics. Changes include:
- The P50 electrode is identical to its predicate with the exception . of default power which falls within the generator specification.
- P90 and CP90 active tip and suction electrode material change. .
- . The CP90 Electrodes is provided with non- handcontrol version as well a handcontrol capability which uses the same fundamental technology as the wired footswitch.
The VAPR VUE Radiofrequency System has been compared to legally marketed devices with respect to intended use, performance and technology characteristic. The VAPR VUE has the same Indications for Use and technology characteristics.
- . . Enhancements on the VAPR VUE generator include:
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- O CP output type
- Open the range of Peak power output O
In addition safety and performance testing have been done to validate the performance and safety of the device. It has been demonstrated that these device modifications will not affect safety and effectiveness of the subject devices.
Verification of the VAPR VUE System and Electrodes includes electrical, Safety and software and performance tests to show that the device meets its product Performance specifications over a range of operating conditions. Validation testing for the VAPR VUE includes testing to show the device meets user needs. Verification testing conform to the following Standards and Guidance documents:
| Standard/Guidance | Description |
|-----------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| EN 60601-1: 1995 | Medical electrical equipment -- Part 1: General<br>requirements for safety |
| EN60601-2-2:2007 | Medical electrical equipment -- Part 2-2:<br>Particular requirements for the safety of high<br>frequency surgical equipment |
| EN60601-1-2: 2006 | Medical electrical equipment -- Part 1-2:<br>General requirements for safety - Collateral<br>standard: Electromagnetic compatibility -<br>Requirements and tests. |
| EN 60601-1-<br>4/A1:2005 | EN 60601-1-4/A1 2005 electrical equipment -<br>Part 1-4: general rules of security - Collateral<br>Standard: electrical systems programmable |
| ISO 60601-1-4 | Medical Electrical Equipment: Part 1-4 General<br>requirements for collateral standard:<br>Programmable electrical medical systems. |
| ISO 62304 | Medical device software-software life cycle<br>process |
| Guidance for the Content of Premarket Submission for Software<br>Contained in Medical Devices: 2005 | |
| General Principals of Software Validation; Final Guidance for<br>Industry and FDA Staff: 2002 | |
| Guidance Off-The-Shelf Software Use in Medical Devices: 1999 | |
#### TABLE 1 Standards & Guidance Documents
#### Clinical Testing
No clinical studies are required to demonstrate safety and efficacy of the device in support of an application for premarket clearance. The VAPR
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VUE Radiofrequency System and Electrodes do not differ from the predicate device in fundamental scientific technology or intended use.
Conclusion
Results of performance and safety testing have demonstrated that the modified device is suitable for its intended use.
Based on the indications for use, fundamental scientific technology, and comparison to the predicate devices, the VAPR VUE Radiofrequency System, along with the Premiere50, Premiere90 and CP90 Electrodes are shown to be substantially equivalent to the predicate devices under the Federal Food, Drug and Cosmetic Act.
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Image /page/5/Picture/0 description: The image shows the seal of the U.S. Department of Health & Human Services. The seal features a stylized caduceus, a symbol often associated with medicine and healthcare, in the center. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular pattern around the caduceus. The seal is black and white.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002
Depuy Mitek, A Johnson & Johnson Company % Ms. Susan Kagan Project Manger, Regulatory Affairs 325 Paramount Drive Raynham, Massachusetts 02767
Re: K100638
Trade/Device Name: VAPR Electrodes
VAPR VUE Radiofrequency System including wireless footswitch and electrodes
JUN 1 8 2010
Regulation Number: 21 CFR 878.4400
Regulation Name: Electrosurgical cutting and coagulation device and accessories Regulatory Class: II Product Code: GEI Dated: June 15, 2010 Received: June 17, 2010
Dear Ms. Kagan:
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
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#### Page 2 - Ms. Susan Kagan
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
Director Division of Surgical, Orthopedic and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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# Indications for Use
510(k) Number (if known):
Device Name: VAPR Electrodes
Indications for Use:
The DePuy Mitek VAPR Electrodes for use with all VAPR Electrosurgical Systems are intended for resection, ablation and excision of soft tissue, hemostasis of blood vessels and coagulation of soft tissue in patients requiring arthroscopic surgery of the knee, shoulder, ankle, elbow, and wrist.
Prescription Use X (Part 21 CFR 801 Subpart D)
.
יי
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
Division Sign-Off
(Division Sig Division of Surgical, Orthopedic, and Restorative Devices
510(k) Number K100638
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## Indications for Use
510(k) Number (if known):
Device Name: VAPR VUE Radiofrequency System including Wireless Footswitch and Electrodes
Indications for Use:
The Mitek VAPR VUE Radiofrequency System is intended for resection, ablation and excision of soft tissue, hemostasis of blood vessels and coagulation of soft tissues in patients requiring arthroscopic surgery of the knee, shoulder, ankle, elbow and wrist.
The DePuy Mitek VAPR Electrodes for use with the VAPR VUE Radiofrequency System are intended for resection, ablation and excision of soft tissue, hemostasis of blood vessels and coagulation of soft tissue in patients requiring arthroscopic surgery of the knee, shoulder, ankle, elbow, and wrist.
Prescription Use (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)
signature
Page 1 of 1
Division of Surgical, Orthopedic, and Restorative Devices
510(k) Number K100638
