FDA 510(k) Application Details - K172430

Device Classification Name	Abutment, Implant, Dental, Endosseous   More FDA Info for this Device
510(K) Number	K172430
Device Name	Abutment, Implant, Dental, Endosseous
Applicant	Argen Corporation 5855 Oberlin Drive SAN DIEGO, CA 92121 US Other 510(k) Applications for this Company
Contact	Paul Cascone Other 510(k) Applications for this Contact
Regulation Number	872.3630   More FDA Info for this Regulation Number
Classification Product Code	NHA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/11/2017
Decision Date	05/18/2018
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