FDA 510(k) Application Details - K123045

Device Classification Name	More FDA Info for this Device
510(K) Number	K123045
Device Name	BRIGADE STANDALONE SYSTEM
Applicant	NUVASIVE, INC. 7475 LUSK BLVD SAN DIEGO, CA 92121 US Other 510(k) Applications for this Company
Contact	Cynthia Adams Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OVD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/01/2012
Decision Date	04/16/2013
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review