WATERLASE MD, MODEL 7100102
Device Facts
| Record ID | K091746 |
|---|---|
| Device Name | WATERLASE MD, MODEL 7100102 |
| Applicant | Biolase Technology, Inc. |
| Product Code | GEX · General, Plastic Surgery |
| Decision Date | Dec 7, 2009 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 878.4810 |
| Device Class | Class 2 |
| Attributes | Therapeutic |
Indications for Use
Removal of subgingival calculi in periodontal pockets with periodontitis by closed or open curettage.
Device Story
Waterlase MD is an Er,Cr:YSGG dental laser system for hard and soft tissue procedures. Input: laser energy delivered via flexible fiber optic to handpiece. Operation: laser energy combined with water atomization spray to cut, remove, contour, or etch tissue; soft tissue modes (H and S) use laser for incision/excision/ablation with water spray for cooling/cleaning. Output: laser beam at target site; visible aiming light; illumination via fiber optic ports. Used in dental clinics by clinicians. Adjustable parameters include power output, pulse duration, repetition rate, and air/water flow. Interchangeable tips vary spot size/geometry. Output allows precise tissue management, potentially improving clinical outcomes compared to traditional techniques.
Clinical Evidence
No clinical data provided; substantial equivalence is based on technological comparison to the predicate device.
Technological Characteristics
Er,Cr:YSGG laser source; flexible fiber optic delivery; water atomization spray system; adjustable power, pulse duration, frequency, and flow rates; interchangeable tips for variable spot size/geometry; visible aiming light; illumination ports.
Indications for Use
Indicated for patients with periodontitis requiring removal of subgingival calculi in periodontal pockets via closed or open curettage. Contraindicated for patients with specific medical conditions including, but not limited to, allergy to local/topical anesthetics, heart disease, lung disease, bleeding disorders, sleep apnea, or immune system deficiency.
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
- Ka Vo Key Laser III (1243 US)
Submission Summary (Full Text)
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CONFIDENTIAL Biolase Technology, Inc.
> Regulatory Authority:
Company:
Contact:
K091746
510k Summary of Safety & Efficacy Waterlase® MD™ Expanded Indications for Use June 11, 2009
510(k) Summary of Safety and Effectiveness Information DEC - 7 2009
Safe Medical Devices Act of 1990, 21 CFR 807.92
Biolase Technology, Inc. 4 Cromwell Irvine, CA 92618
Ms. Ioana M. Rizoiu Biolase Technology, Inc. 4 Cromwell Irvine, CA 92618 Tel: (949) 226-8144 Fax: (949) 273-6680
Waterlase®MD Trade Name: Common Name: Er, Cr: YSGG laser Classification Name: Surgical laser instrument Classification Code: 79 GEX, MXF, DZI a Class II device Equivalent Devices: Ka Vo Key Laser III 1243 US
### DEVICE DESCRIPTION:
The Waterlase MD dental laser system is a device used to perform a variety of dental soft and hard tissue indications. For hard tissue procedures the Waterlase MD uses the Erbium,Chromium:Yttrium,Scandium,Gallium Garnet (Er,Cr.YSGG) laser in combination with advanced water atomization spray technology to cut, remove, shave, contour, roughen and etch tissues. Soft tissue procedures are performed using two different modes of operation. H and S. where direct Er.Cr. YSGG laser energy is applied to incise, excise or ablate these tissues. For soft tissue procedures the water spray is applied for hydration. cooling or to keep tissues and the field of view clean. For hard tissue applications the spray is part of the tissue removing process as well as hydration, cooling and keeping tissues and field of view clean.
A flexible fiber optic terminated into the handpiece delivers the Waterlase®MD laser energy to the end fiber tip and target. A visible aiming light emitted from the handpiece's distal end pinpoints the area of treatment. Three fiber optic ports provide illumination from the handpiece to the tissue site in addition to the center beam emitting source. In both hard and soft tissue applications the power output, pulse duration, repetition rate (frequency) and air and water flow rates are adjustable to specific user requirements. The spot size and spot geometry can also be varied by changing tips which include different diameters and end configurations.
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CONFIDENTIAL Biolase Technology, Inc.
K091746
510k Summary of Safety & Efficacy
Waterlase MD™ Expanded Indications for Use
June 11, 2009
# INDICATIONS FOR USE:
Removal of subgingival calculi in periodontal pockets with periodontitis by closed or open curettage.
### CONTRAINDICATIONS, WARNINGS AND PRECAUTIONS:
All clinical procedures performed with Waterlase MD must be subject to the same clinical judgment and care as with traditional techniques. Patient risk must always be considered and fully understood before clinical treatment. The clinician must completely understand the patient's medical history prior to treatment. Exercise caution for general medical conditions, which might contraindicate a local procedure. Such conditions may include, but are not limited to, allergy to local or topical anesthetics, heart disease, lung disease, bleeding disorders, sleep apnea or an immune system deficiency. Medical clearance from patient's physician is advisable when doubt exists regarding treatment.
### SUBSTANTIAL EQUIVALENCE:
The indications included herein are the same as indications that have been previously cleared by the FDA for an equivalent device. Substantial equivalency for the Waterlase MD has been determined through comparison to a previously cleared device.
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Food and Drug Administration 10903 New Hampshire Avenue Document Control Room W-066-0609 Silver Spring, MD 20993-0002
DEC - 7 2009
Ms. Ioana M. Rizoiu Vice President, Clinical Research & Development Biolase Technology, Incorporated 4 Cromwell Irvine, California 92618-1816
Re: K091746 Trade/Device Name: Waterlase® MD Regulation Number: 21CFR 878.4810 Regulation Name: Laser Surgical Instrument for use in General and Plastic Surgery and in Dermatology Regulatory Class: II Product Code: GEX Dated: November 18, 2009 Received: November 24, 2009
Dear Ms. Rizoiu:
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.
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## Page 2- Ms. Rizoiu
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.
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.
h for
Susan Runner, D.D.S., M.A. Acting Division Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
#### Enclosure
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K091746
Page 1 of 1
Indications for Use
510(k) Number_
Device Name: Waterlase® MD
Indications for Use:
Removal of subgingival calculi in periodontal pockets with periodontitis by closed or open curettage.
X Prescription Use (Part 21 CFR 801 Subpart D) AND/OR
Over-the-Counter Use_ (21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Kein Muluy for NSP
(Division Sign-Off) Division of Anesthesialagy, Gerleral Hospital Tection Control, Dental Devices
510(k) Number: K 091746
