FDA 510(k) Application Details - K081751

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K081751
Device Name	Implant, Endosseous, Root-Form
Applicant	ADIN DENTAL IMPLANTS SYSTEM LTD INDUSTRIAL PARK 13 M.P. MISGAV MIZPE AVIV 20187 IL Other 510(k) Applications for this Company
Contact	BENNY ARAZY 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	06/19/2008
Decision Date	12/19/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review