Medilas H RFID Laser Fibers

K152591 · Dornier Medtech America, Inc. · GEX · Oct 8, 2015 · General, Plastic Surgery

Device Facts

• Record ID: K152591
• Device Name: Medilas H RFID Laser Fibers
• Applicant: Dornier Medtech America, Inc.
• Product Code: GEX · General, Plastic Surgery
• Decision Date: Oct 8, 2015
• Decision: SESE
• Submission Type: Special
• Regulation: 21 CFR 878.4810
• Device Class: Class 2
• Attributes: Therapeutic

Intended Use

Dornier's Medilas H RFID Laser Fibers are intended to be used as an accessory to the Dornier Medilas H Holmium Laser ("Laser"). This laser is intended for cutting, vaporization, ablation, and coagulation of soft tissue in conjunction with endoscopic equipment (including laparoscopes, hysteroscopes, bronchoscopes, gastroscopes, and colonoscopes), or for open surgery for contact or non-contact surgery with or without a handpiece for use in incision/excision, vaporization, ablation and coagulation of soft tissue. The Laser is indicated for use in medicine and surgery, in the following medical specialties: Arthroscopy, Urology, Lithotripsy, Pulmonology, Gastroenterology, Gynecology, ENT, General Surgery.

Device Story

Accessory fiber for Dornier Medilas H Holmium Laser; delivers laser energy to target soft tissue. Used in endoscopic or open surgical procedures; operated by physicians. Modification of existing fiber design to include reduced outer diameter. Fiber functions as light guide for laser energy; enables incision, excision, vaporization, ablation, and coagulation. Benefits include precise tissue management during surgery. No changes to principle of operation or materials compared to predicate.

Clinical Evidence

Bench testing only. Performance data included power transmission testing, durability stress testing, eccentricity testing, and visual inspections, utilizing the same methods as the predicate device.

Technological Characteristics

Silica core and cladding fiber; accessory to Holmium laser system. Designed for laser energy delivery. Identical materials and manufacturing processes to predicate. No electronic components or software algorithms.

Indications for Use

Indicated for patients requiring soft tissue cutting, vaporization, ablation, or coagulation during endoscopic or open surgical procedures across specialties including arthroscopy, urology, lithotripsy, pulmonology, gastroenterology, gynecology, ENT, and general surgery.

Regulatory Classification

Identification

(1) A carbon dioxide laser for use in general surgery and in dermatology is a laser device intended to cut, destroy, or remove tissue by light energy emitted by carbon dioxide.(2) An argon laser for use in dermatology is a laser device intended to destroy or coagulate tissue by light energy emitted by argon.

Predicate Devices

• Dornier Medilas H RFID Laser Fiber (K121938)

Reference Devices

• Bard Endobeam Laser Fibers (K120926)

Submission Summary (Full Text)

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Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002

Dornier MedTech America Incorporated Mr. John Hoffer Vice President Quality, Regulatory, Clinical 1155 Roberts Boulevard, Suite 100 Kennesaw, Georgia 30144

October 8, 2015

Re: K152591 Trade/Device Name: Dornier Medilas H RFID Laser Fiber Regulation Number: 21 CFR 878.4810 Regulation Name: Laser surgical instrument for use in general and plastic surgery and in dermatology Regulatory Class: Class II Product Code: GEX Dated: September 9, 2015 Received: September 10, 2015

Dear Mr. Hoffer:

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 [SELECT ONE: Part 801 [or, for IVDs only] Parts 801 and 809]); medical device reporting of medical device-related adverse events) (21 CFR

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803); good manufacturing practice requirements as set forth in the quality systems (OS) 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 contact the Division of Industry and Consumer Education at its toll-free number [phone] or [phone] or at its Internet address

http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. 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 Industry and Consumer Education at its toll-free number [phone] or [phone] or at its Internet address

http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.

Sincerely yours,

Joshua C. Nipper -S

Binita S. Ashar, M.D., M.B.A., F.A.C.S. For Director

Division of Surgical Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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### Indications for Use Statement

# DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

#### Indications for Use

Form Approved: OMB No. 0910-0120 Expiration Date: January 31, 2017 See PRA Statement on last page

510(k) Number (if known)

K152591

#### Device Name Dornier Medilas H RFID Laser Fiber

Indications for Use (Describe)

Dornier's Medilas H RFID Laser Fibers are intended to be used as an accessory for the Dornier Medilas H Holmium Laser ("Laser"). This laser is intended for cutting, vaporization, and coagulation of soft tissue in conjunction with endoscopic equipment (including laparoscopes, bronchoscopes, gastroscopes, cystoscopes, and colonoscopes), or for open surgery for contact surgery with or without a handpiece for use in incision/excision, vaporization, ablation of soft tissue. The Laser is indicated for use in medicine and surgery, in the following medical specialties:

- Arthroscopy ●
- Urology ●
- . Lithotripsv
- Pulmonology ●
- Gastroenterology ●
- Gynecology ●
- . ENT
- General Surgery

Type of Use (Select one or both, as applicable)

X Prescription Use (Part 21 CFR 801 Subpart D)

□ Over-The-Counter Use (21 CFR 801 Subpart C)

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#### FOR FDA USE ONLY

Concurrence of Center for Devices and Radiological Health (CDRH) (Signature)

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FORM FDA 3881 (1/14)

Page 1 of 1 FDA

PSC Publishing Services [phone] EF

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### 510(k) SUMMARY

#### Dornier's Medilas H RFID Laser Fiber

### Submitter's Name, Address, Telephone Number, Contact Person and Date Prepared

| Dornier MedTech America | Phone: [phone] |
|-------------------------|----------------------------------|
| 1155 Roberts Blvd. | Fax: [phone] |
| Kennesaw, GA 30144 | Date Prepared: September 1, 2015 |

Phone: [phone] Contact Person: John Hoffer

#### Name of Device and Name/Address of Sponsor

Medilas H RFID Laser Fibers John Hoffer Dornier MedTech America 1155 Roberts Blvd. Kennesaw, GA 30144

#### Common or Usual Name

Holmium Laser Fibers

#### Classification Name

Laser Instrument, (Accessory); Product Code: GEX

### Predicate and Reference Devices

Dornier Medilas H RFID Laser Fiber (K121938) (Primary predicate device) Bard Endobeam Laser Fibers (K120926)

### Purpose of the Special 510(k) notice.

The Medilas H RFID Laser Fiber is a modification to Dornier's currently cleared Dornier Medilas H RFID Laser Fibers (K121938) to include a fiber with a reduced outer diameter.

#### Intended Use/Indications for Use

Dornier's Medilas H RFID Laser Fibers are intended to be used as an accessory to the Dornier Medilas H Holmium Laser ("Laser"). This laser is intended for cutting, vaporization, ablation, and coagulation of soft tissue in conjunction with endoscopic equipment (including laparoscopes, hysteroscopes, bronchoscopes, gastroscopes, and colonoscopes), or for open surgery for contact or non-contact surgery with or without a handpiece for use in incision/excision, vaporization, ablation and coagulation of soft tissue. The Laser is indicated for use in medicine and surgery, in the following medical specialties:

- Arthroscopy, ●
- . Urology,

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- Lithotripsy, ●
- Pulmonology, ●
- . Gastroenterology,
- Gynecology,
- ENT,
- General Surgery.

## Technological Characteristics

The Dornier's Medilas H RFID Laser Fiber has the same technological characteristics and principles of operation as the predicate devices. The fiber core and cladding for the subject device are made from silica, which is same material used in all the predicate devices. Additionally, the fiber is manufactured and tested in the identical fashion as the company's predicate device and functions in an equivalent manner.

## Performance Data

Nonclinical functional performance testing was conducted per internal test methods. The functional testing included:

- . Power transmission testing
- . Durability Stress Testing
- . Eccentricity Testing
- Visual Inspections ●

These methods were the same as used for the cleared predicate.

### Substantial Equivalence

Dornier's Medilas H RFID Laser Fiber has the same intended use/indications for use, as well as technological characteristics and principles of operation as the predicate devices. The minor difference of laser fiber outer diameter size does not raise any new questions of safety or effectiveness. Performance data demonstrates that the Dornier Medilas H RFID Laser Fibers are substantially equivalent to the listed company predicate device. Thus, the Dornier Medilas H RFID Laser Fibers are substantially equivalent to its predicate and reference devices.