meddevicedb.com FDA Device Reference

DYRACT EXTRA RESTORATIVE

K050880 Class II Special
Decision Date
2005-04-22
Sponsor / Applicant
Dentsply Intl.

Technical Specification

510(k) Submission ID K050880
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2005-04-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DYRACT EXTRA RESTORATIVE received FDA 510(k) clearance under submission number K050880, sponsored by Dentsply Intl.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2005-04-22.

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.