NAVI ROOT
Device Facts
| Record ID | K083901 |
|---|---|
| Device Name | NAVI ROOT |
| Applicant | S-Denti Co., Ltd. |
| Product Code | LQY · DE |
| Decision Date | Apr 15, 2009 |
| Decision | SESE |
| Submission Type | Traditional |
| Device Class | Class U |
Indications for Use
The NAVI ROOT is intended for measuring the length of the root canal for the purpose of performing root canals.
Device Story
NAVI ROOT is an electronic apex locator used by dentists during endodontic procedures. It measures root canal length to assist in accurate instrumentation and filling. The device provides real-time feedback to the clinician, allowing for precise determination of the apical constriction. By ensuring accurate measurement, it helps prevent over-instrumentation or under-filling of the canal, potentially improving clinical outcomes and patient comfort during root canal therapy.
Clinical Evidence
No clinical data provided; bench testing only.
Technological Characteristics
Electronic apex locator for dental use. Operates via electrical impedance measurement to determine root canal length. Standalone device.
Indications for Use
Indicated for patients requiring root canal procedures to measure root canal length.
Submission Summary (Full Text)
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## DEPARTMENT OF HEALTH & HUMAN SERVICES
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## Public Health Service
APR 1 5 2009
Food and Drug Administration 200 Corporate Boulevard Rockville MD 20850
S-Denti Company, Limited C/o Mr. Kevin Walls, RAC Principal Consultant Regulatory Insight, Incorporated 5401 South Cottonwood Court Greenwood Village, Colorado 80121
Re: K083901 Trade/Device Name: NAVI ROOT Regulation Number: (Not Classified) Regulatory Class: II Product Code: LQY Dated: April 6, 2009 Received: April 7, 2009
Dear Mr. Walls:
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 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- Mr. Walls
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Center for Devices and Radiological Health's (CDRH's) Office of Compliance at (240) 276-. 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 contact the CDRH/Office of Surveillance and Biometrics/Division of Postmarket Surveillance at 240-276-3464. For more information regarding the reporting of adverse events, please go to http://www.fda.gov/cdrh/mdr/.
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 (240) 276-3150 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely yours,
Suren Sunoer
Susan Runner, D.D.S., MA Acting 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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K083901
Indications for Use
510(k) Number (if known): K083901
Device Name: NAVI ROOT
Indications for Use: The NAVI ROOT is intended for measuring the length of the root canal for the purpose of performing root canals.
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 OF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Susan Berger
(Division Sign-Off) (Division of Anesthesiology, General Hospital Infection Control, Dental Devices
510(k) Number. K063901
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