Clearance Summary
Surgic Pro, Surgic Pro+ received FDA 510(k) clearance under submission number K173905, sponsored by Nakanishi, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2018-06-19.
- Submission: K173905
- Applicant / Sponsor: Nakanishi, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4200
- Decision date: 2018-06-19
Classification & Regulation
This clearance is catalogued under FDA product code EBW and 21 CFR 872.4200, within the Dental review panel as a Class I device.