FDA 510(k) Application Details - K020062

Device Classification Name	Alloy, Metal, Base   More FDA Info for this Device
510(K) Number	K020062
Device Name	Alloy, Metal, Base
Applicant	METALOR TECHNOLOGIES USA 255 JOHN L. DIETSCH BLVD. NORTH ATTLEBOROUGH, MA 02761 US Other 510(k) Applications for this Company
Contact	BRUCE A BARTON 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	01/08/2002
Decision Date	02/14/2002
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