FDA 510(k) Application Details - K070562

Device Classification Name	Abutment, Implant, Dental, Endosseous   More FDA Info for this Device
510(K) Number	K070562
Device Name	Abutment, Implant, Dental, Endosseous
Applicant	MEGAGEN CO., LTD. 13340 E. FIRESTONE BLVD. SUITE J SANTA FE SPRINGS, CA 90670 US Other 510(k) Applications for this Company
Contact	DAE K CHANG 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	02/27/2007
Decision Date	05/18/2007
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