FDA 510(k) Application Details - K180859

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K180859
Device Name	Implant, Endosseous, Root-Form
Applicant	DenTack Implants Ltd 24 HaTa'as St. POB 2405 Kfar-Saba 4464102 IL Other 510(k) Applications for this Company
Contact	Tali Hazan 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	04/02/2018
Decision Date	12/13/2018
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