FDA 510(k) Application Details - K012839

Device Classification Name	Alloy, Gold-Based Noble Metal   More FDA Info for this Device
510(K) Number	K012839
Device Name	Alloy, Gold-Based Noble Metal
Applicant	WIELAND EDELMETALLE GMBH & CO. SCHWENNINGER STRABE 13 D-75179 PFORZHEIM DE Other 510(k) Applications for this Company
Contact	GERHARD P0LZER Other 510(k) Applications for this Contact
Regulation Number	872.3060   More FDA Info for this Regulation Number
Classification Product Code	EJT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/23/2001
Decision Date	12/31/2001
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