FDA 510(k) Application Details - K131557

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K131557
Device Name	Implant, Endosseous, Root-Form
Applicant	RITTER IMPLANTS GMBH CO KG 57 LAZY BROOK RD MONROE, CT 06468 US Other 510(k) Applications for this Company
Contact	RAYMOND KELLY 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	05/29/2013
Decision Date	05/09/2014
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