meddevicedb.com FDA Device Reference

FUSION PUTTY TYPE

K043493 Class II Traditional
Decision Date
2005-03-04
Sponsor / Applicant
GC America, Inc.

Technical Specification

510(k) Submission ID K043493
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 2005-03-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FUSION PUTTY TYPE received FDA 510(k) clearance under submission number K043493, sponsored by GC America, 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 2005-03-04.

Classification & Regulation

This clearance is catalogued under FDA product code ELW and 21 CFR 872.3660, within the Dental review panel as a Class II device.