FDA 510(k) Application Details - K181266

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K181266
Device Name	Implant, Endosseous, Root-Form
Applicant	Novodent SA Y-PARC Technopole Avenue des Sciences 11 Yverdons-les-Bains CH1400 CH Other 510(k) Applications for this Company
Contact	Cem Kocer 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	05/14/2018
Decision Date	11/01/2018
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