FDA 510(k) Application Details - K040205

Device Classification Name	Abutment, Implant, Dental, Endosseous   More FDA Info for this Device
510(K) Number	K040205
Device Name	Abutment, Implant, Dental, Endosseous
Applicant	INTRA-LOCK INTERNATIONAL 1200 NORTH FEDERAL HWY SUITE 200 BOCA RATON, FL 33432 US Other 510(k) Applications for this Company
Contact	JEFFERY SAKOFF 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	01/30/2004
Decision Date	03/22/2004
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