meddevicedb.com FDA Device Reference

COMPOSITE RESTORATION MATERIAL

K031721 Class II Traditional
Decision Date
2003-09-11
Sponsor / Applicant
Milton Hodosh, M.D.

Technical Specification

510(k) Submission ID K031721
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2003-09-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMPOSITE RESTORATION MATERIAL received FDA 510(k) clearance under submission number K031721, sponsored by Milton Hodosh, M.D.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2003-09-11.

Classification & Regulation

This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.