FDA 510(k) Application Details - K142079

Device Classification Name	More FDA Info for this Device
510(K) Number	K142079
Device Name	STALIF CTI, STALIF C
Applicant	CENTINEL SPINE, INC. 1331 H STREET NW, 12TH FLOOR WASHINGTON, DC 20005 US Other 510(k) Applications for this Company
Contact	JUSTIN EGGLETON Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OVE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/31/2014
Decision Date	10/24/2014
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review