FDA 510(k) Application Details - K031719

Device Classification Name	Abutment, Implant, Dental, Endosseous   More FDA Info for this Device
510(K) Number	K031719
Device Name	Abutment, Implant, Dental, Endosseous
Applicant	NOBEL BIOCARE AB 22715 SAVI RANCH PKWY. YORBA LINDA, CA 92887 US Other 510(k) Applications for this Company
Contact	ELIZABETH J MASON Other 510(k) Applications for this Contact
Regulation Number	872.3630   More FDA Info for this Regulation Number
Classification Product Code	NHA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/03/2003
Decision Date	07/02/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review