FDA 510(k) Application Details - K092112

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K092112
Device Name	Implant, Endosseous, Root-Form
Applicant	B.T.I. BIOTECHNOLOGY INSTITUTE, S.L. LEONARDO DA VINCI 14 B MINANO(ALAVA) 01510 ES Other 510(k) Applications for this Company
Contact	ALFREDO GOMEZ 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	07/14/2009
Decision Date	10/06/2009
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