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Well-Root ST

K170950 Class II Traditional
Decision Date
2017-12-20
Sponsor / Applicant
Vericom Co., Ltd.

Technical Specification

510(k) Submission ID K170950
Product Code KIF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3820
Decision Date 2017-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Well-Root ST received FDA 510(k) clearance under submission number K170950, sponsored by Vericom Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2017-12-20.

Classification & Regulation

This clearance is catalogued under FDA product code KIF and 21 CFR 872.3820, within the Dental review panel as a Class II device.