FDA 510(k) Application Details - K193434

Device Classification Name	Powder, Porcelain   More FDA Info for this Device
510(K) Number	K193434
Device Name	Powder, Porcelain
Applicant	VITA Zahnfabrik GmbH H Rauter & Co Spitelgasse 3 Bad Sackingen D-79713 DE Other 510(k) Applications for this Company
Contact	Bernd Walker Other 510(k) Applications for this Contact
Regulation Number	872.6660   More FDA Info for this Regulation Number
Classification Product Code	EIH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/11/2019
Decision Date	07/21/2020
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review