FDA 510(k) Application Details - K021969

Device Classification Name	Alloy, Metal, Base   More FDA Info for this Device
510(K) Number	K021969
Device Name	Alloy, Metal, Base
Applicant	NEIRYNCK & VOGT NV 12960 STONECREEK DR. PICKERINGTON, OH 43147 US Other 510(k) Applications for this Company
Contact	JOSH ANDRACHEK Other 510(k) Applications for this Contact
Regulation Number	872.3710   More FDA Info for this Regulation Number
Classification Product Code	EJH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/17/2002
Decision Date	07/30/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review