MAGNATEK C-300

K981310 · Magna Advanced Technologies, Inc. · GEI · Jul 9, 1998 · General, Plastic Surgery

Device Facts

• Record ID: K981310
• Device Name: MAGNATEK C-300
• Applicant: Magna Advanced Technologies, Inc.
• Product Code: GEI · General, Plastic Surgery
• Decision Date: Jul 9, 1998
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 878.4400
• Device Class: Class 2
• Attributes: Therapeutic

Intended Use

C-300 Coagulator is used in small surgical procedures in The dermatology, plastic surgery and general surgery in order to only coagulate (burn) an open wound or skin lesions. This device does cut the skin, it only closes open wounds or lesions by not coagulating (burning) the skin in any of the small surgical procedures mentioned above. Federal Law restricts the use of this device by or on the order of a qualified physician only.

Device Story

MagnaTek C-300 is a coagulator device used in dermatology, plastic surgery, and general surgery. It functions by coagulating (burning) open wounds or skin lesions to achieve hemostasis. The device is operated by a qualified physician in a clinical setting. It provides a thermal effect to close wounds. The device does not cut skin. It benefits patients by facilitating wound closure during minor surgical procedures.

Clinical Evidence

No clinical data provided; bench testing only.

Technological Characteristics

Electrosurgical coagulator for thermal tissue treatment. Device is a standalone unit. Technical specifications and materials not detailed in the provided documentation.

Indications for Use

Indicated for use in dermatology, plastic surgery, and general surgery for coagulation of open wounds or skin lesions in small surgical procedures. Restricted to use by or on the order of a qualified physician.

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.

Submission Summary (Full Text)

{0}------------------------------------------------

Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo is circular, with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" arranged around the top half of the circle. Inside the circle is an abstract symbol that resembles an eagle or a stylized human figure.

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

0 1698 JUL

Ms. Annie Velez · Directory of Regulatory Affairs Magna Advanced Technologies, Inc. 7200 N.W. Seventh Street Miami, Florida 33126

Re: K981310 Trade Name: MagnaTek C-300 Regulatory Class: II Product Code: GEI Dated: March 4, 1998 Received: April 10, 1998

Dear Ms. Velez:

We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to 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). 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 (Premarket Approval), 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 895. A substantially equivalent determination assumes compliance with the current Good Manufacturing Practice requirement, as set forth in the Quality System Regulation (OS) for Medical Devices: General regulation (21 CFR Part 820) and that, through periodic (QS) inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations.

This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.

{1}------------------------------------------------

Page 2 - Ms. Annie Velez

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at [phone]. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at [phone]. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number [phone] or [phone] or at its internet address "http://www.fda.gov/cdrh/dsmamain.html".

Sincerely yours,

Celia M. Witten, Ph.D., M.D. Director Division of General and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

{2}------------------------------------------------

305 261 4492

## INDICATION FOR USE STATEMENT

510(k) Number: Not yet available \(9)3\D

Coagulator Device Name:

Device Model: C-300

Indications for Use:

C-300 Coagulator is used in small surgical procedures in The dermatology, plastic surgery and general surgery in order to only coagulate (burn) an open wound or skin lesions. This device does cut the skin, it only closes open wounds or lesions by not coagulating (burning) the skin in any of the small surgical procedures mentioned above.

Federal Law restricts the use of this device by or on the order of a qualified physician only.

| Concurrence of CDRH, Office of Device Evaluation (ODE) | |
|--------------------------------------------------------|-----------------------------------------|
| | (Division Sign-Off) |
| | Division of General Restorative Devices |
| 510(k) Number | K981310 |