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PIEZOSURGERY TOUCH

K122322 Class II Traditional
Decision Date
2012-12-06
Sponsor / Applicant
Mectron S.P.A.

Technical Specification

510(k) Submission ID K122322
Product Code DZI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4120
Decision Date 2012-12-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PIEZOSURGERY TOUCH received FDA 510(k) clearance under submission number K122322, sponsored by Mectron S.P.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2012-12-06.

Classification & Regulation

This clearance is catalogued under FDA product code DZI and 21 CFR 872.4120, within the Dental review panel as a Class II device.