FDA 510(k) Application Details - K111189

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K111189
Device Name	Implant, Endosseous, Root-Form
Applicant	SYNTEC SCIENTIFIC CORP. 3F1. 96 CHUNG HSIAO E. RD. SEC. 3 TAIPEI CITY 106 TW Other 510(k) Applications for this Company
Contact	CHIA-CHING LEE 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	04/28/2011
Decision Date	12/20/2012
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