HALOFLEX ENERGY GENERATOR, MODELS 1190A-115A AND 1190A-230A
Device Facts
| Record ID | K092487 |
|---|---|
| Device Name | HALOFLEX ENERGY GENERATOR, MODELS 1190A-115A AND 1190A-230A |
| Applicant | Barrx Medical, Incorporated |
| Product Code | GEI · General, Plastic Surgery |
| Decision Date | Nov 10, 2009 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 878.4400 |
| Device Class | Class 2 |
| Attributes | Therapeutic |
Indications for Use
The HALOFLEX Energy Generator is indicated for use for the coagulation of soft tissue. The HALOFLEX Energy Generator intended use is for coagulation of soft tissue, and bleeding on non bleeding sites in the gastrointestinal tract. The HALORLEX Energy Generator is indicated for use in the coagulation of bleeding and non-bleeding sites in the gastrointestinal tract including, but not limited to, the esophagus. Indications include Esophageal Ulcers, Mallory-Weiss tears, Arteriovenous Malformations, Angiomata, Barrett's Esophagus, Dieulafoy Lesions, and Angiodysplasia.
Device Story
HALOFLEX Energy Generator is an electrosurgical coagulation system; provides RF energy for soft tissue coagulation in GI tract. Modification of HALO360/HALO90 generators; integrates multiple generator functions onto single hardware platform. Input: electrical power; Output: RF energy for coagulation. Used in clinical settings by physicians. Design changes include CPU board with increased memory, consolidated pressure monitoring/RF MUX boards, and updated software for specific performance characteristics. Device maintains same fundamental scientific technology and clinical parameters as predicates; safety mechanisms remain unchanged. Benefits include reliable soft tissue coagulation and treatment of various GI lesions.
Clinical Evidence
Bench testing only. Performance testing conducted in compliance with international and domestic requirements demonstrated the device is at least as safe and effective as the predicate HALO360 and HALO90 generators.
Technological Characteristics
Electrosurgical coagulation system. Features: CPU board with increased memory, consolidated Pressure Monitoring and RF MUX boards, integrated hardware platform for HALO360/HALO90 functionality. Energy source: RF. Software: updated codes for specific performance characteristics. Sterilization: not specified.
Indications for Use
Indicated for coagulation of soft tissue and bleeding/non-bleeding GI tract sites (e.g., esophagus). Includes treatment for Esophageal Ulcers, Mallory-Weiss tears, Arteriovenous Malformations, Angiomata, Barrett's Esophagus, Dieulafoy Lesions, and Angiodysplasia.
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
- HALO360 Energy Generator model 1100C-115B (K051168)
- HALO® Energy Generator model 1100C-115C (K060169, K062441)
- RF 3000 Radiofrequency Generator (K000241)
Submission Summary (Full Text)
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K092487)
NOV 1 0 2009
#### 510(k) SUMMARY
## BÂRRX Medical Inc.'s HALORLEX Energy Generator
## Submitter's Name, Address, Telephone Number, Contact Person and Date Prepared
BARRX Medical Inc. 540 Oakmead Parkway Sunnyvale, CA 94085
| Phone: | 408-328-7302 |
|------------|--------------|
| Facsimile: | 408-328-7395 |
Viorica (Vivi) Filimon Contact Person:
Date Prepared: August 12, 2009
#### Name of Device and Name/Address of Sponsor
HALOFLEX Energy Generator
BÂRRX Medical Inc. 540 Oakmead Parkway Sunnyvale, CA 94085
#### Common or Usual Name:
Electrosurgical Coagulation System
#### Classification Name
878.4400 Electrosurgical, cutting & coagulation & accessories, product code GEI
#### Predicate Devices
HALO360 Energy Generator model 1100C-115B
HALO® Energy Generator model 1100C-115C
HALO90 Energy Generator model 90-9000
RF 3000 Radiofrequency Generator
BÂRRX Medical Inc.
BARRX Medical Inc.
BARRX Medical Inc.
Radio Therapeutics Corporation (Boston Scientific Inc)
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## Intended Use / Indications for Use
The HALOFLEX Energy Generator is indicated for use for the coagulation of soft tissue
The HALOFLEX Energy Generator intended use is for coagulation of soft tissue, and bleeding on non bleeding sites in the gastrointestinal tract.
The HALORLEX Energy Generator is indicated for use in the coagulation of bleeding and non-bleeding sites in the gastrointestinal tract including, but not limited to, the esophagus. Indications include Esophageal Ulcers, Mallory-Weiss tears, Arteriovenous Malformations, Angiomata, Barrett's Esophagus, Dieulafoy Lesions, and Angiodysplasia.
## Technological Characteristics
The HALORLEX Energy Generator is a modification to the HALO360 Energy Generator and HALO® Energy Generators that have already been cleared by the Food and Drug Administration ("FDA" or the "Agency") for use in coagulation of bleeding and non-bleeding sites in the gastrointestinal tract including but not limited to the esophagus (K051168 and K060169, K062441 respectively). The Generator has the same intended use and fundamental scientific technology as the cleared HALO360 and HALO90 Energy Generators. In addition, the intended use was expanded to include "coagulation of soft tissue", for this indication for use the predicate device is the RF 3000 Radiofrequency Generator (K000241).
The design changes between the HALO360 and HALO® Energy Generators and the HALOFLEX Energy Generator do not affect the clinical parameters employed in the energy delivery or the safety mechanisms that control those parameters.
The HALOFLEX Energy Generator has a limited number of design changes compared to the predicate devices. These changes are minor and do not raise no questions or effectiveness. Further, bench testing demonstrated comparable performance and safety. These modifications were as follows:
- Add to the indications for use the "coagulation of soft tissue", to reflect the . general nature of the device.
- Modification of the CPU board, for increased memory .
- Consolidation of the Pressure Monitoring Board and RF MUX Board in the Hand Piece Interface Board
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- Integration on the HALO360 and HALO90 Energy Generators on the same . hardware platform as HALO360 Energy Generator
- . Update the software codes to reflect the specific performance characteristics for each Energy Generator.
- Optimization of components for reliability, and/or obsolescence
## Performance Data
The HALOFLEX Energy Generator is technologically equivalent and clinically identical to the cleared HALO360 and HALO90 Energy Generators.
Performance testing was conducted in compliance with the applicable international and domestic requirements and the certifications (for harmonized standards) and the reports for performance testing were provided to FDA to support this submission. That data demonstrated that, when used in accordance with the instructions, the HALOFLEX is at least as safe and effective as the predicate devices HALO360 and HALO90 Energy Generators.
### Substantial Equivalence
The HALOFLEX Energy Generator is as safe and effective as the HALO360 Energy Generator (K051168) and HALO90 Energy Generator (K060169 and K062441), RF 3000 Radiofrequency Generator (K000241) the predicate devices. The HALOFLEX Energy Generator has the same intended uses and indications, technological characteristics, and principles of operation as its predicate device. The minor technological differences between the HALORLES Energy Generator and its predicate devices raise no new issues of safety or effectiveness. Performance data demonstrate that the HALOFLEX Energy Generator is as safe and effective as HALO360 Energy Generator (K051168) and HALO90 Energy Generator (K060169 and K062441), RF 3000 Radiofrequency Generator the predicate devices. Thus, the HALOFLEX Energy Generator is substantially equivalent.
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Food and Drug Administration 10903 New Hampshire Avenue Document Control Room W-O66-0609 Silver Spring, MD 20993-0002
BARRX Medical, Inc. % Ms. Viorica Filimon Vice President of Quality/Regulatory Affairs 540 Oakmead Parkway Sunnyvale, California 94085
NOV 1 0 2009
Re: K092487
Trade/Device Name: HALOFLEX Energy Generator Model 1190A-115A Regulation Number: 21 CFR 878.4400 Regulation Name: Electrosurgical cutting and coagulation device and accessories Regulatory Class: II Product Code: GEI Dated: August 12, 2009 Received: August 13, 2009
Dear Ms. Filimon:
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 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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Page 2 – Ms. Viorica Filimon
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/ResourcesforYou/Industry/default.htm.
Sincerely vours.
Sincerely yours,
Mark N Milliken
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 Statement
510(k) Number (if known):_____________________________________________________________________________________________________________________________________________________
Device Name:
Indications for Use:
The HALOFLEX Energy Generator is indicated for use for the coagulation of soft tissue.
The HALOFLEX Energy Generator is indicated for use in the coagulation of bleeding and non-bleeding sites in the gastrointestinal tract including, but not limited to, the esophagus. Indications include Esophageal Ulcers, Mallory-Weiss tears, Arteriovenous Malformations, Angiomata, Barrett's Esophagus, Die Hotor Lesions, and Angiodysplasia.
AND/OR
Prescription Use _ X Use (Part 21 C.F.R. 801 Subpart D)
Over-The-Counter
(21 C.F.R. 807 Subpart C)
# (PLEASE DO NOT WRITE BELOW THIS LINE -- CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
FOR M. MELKERSON
Division of Surgical, Orthopedic, and Restorative Devices
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510(k) Number K01248
