meddevicedb.com FDA Device Reference

TENDER FIBER

K063170 Class II Traditional
Decision Date
2007-01-12
Sponsor / Applicant
Micerium S.P.A.

Technical Specification

510(k) Submission ID K063170
Product Code EBI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3760
Decision Date 2007-01-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TENDER FIBER received FDA 510(k) clearance under submission number K063170, sponsored by Micerium 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 2007-01-12.

Classification & Regulation

This clearance is catalogued under FDA product code EBI and 21 CFR 872.3760, within the Dental review panel as a Class II device.