FDA 510(k) Application Details - K123929

Device Classification Name	Alloy, Metal, Base   More FDA Info for this Device
510(K) Number	K123929
Device Name	Alloy, Metal, Base
Applicant	BEGO BREMER GOLDSCHLAEGEREI WILH. HERBST GMBH & CO WILHELM-HERBST-STRASSE 1 BREMEN 28359 DE Other 510(k) Applications for this Company
Contact	HEIKE GUSTKE 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	12/20/2012
Decision Date	03/14/2013
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review