FDA 510(k) Application Details - K032302

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K032302
Device Name	Implant, Endosseous, Root-Form
Applicant	FRIADENT GMBH 21911 ERIE LN. LAKE FOREST, CA 92630 US Other 510(k) Applications for this Company
Contact	CAROL PATTERSON Other 510(k) Applications for this Contact
Regulation Number	872.3640   More FDA Info for this Regulation Number
Classification Product Code	DZE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/25/2003
Decision Date	10/02/2003
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