FDA 510(k) Application Details - K062931

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K062931
Device Name	Implant, Endosseous, Root-Form
Applicant	LEADER ITALIA S.R.L. 1349 LEXINGTON AVE. NEW YORK, NY 10128 US Other 510(k) Applications for this Company
Contact	HENRY J VOGELSTEIN 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	09/28/2006
Decision Date	11/28/2007
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