FDA 510(k) Application Details - K131784

Device Classification Name	More FDA Info for this Device
510(K) Number	K131784
Device Name	RANGE SPINAL SYSTEM
Applicant	K2M, INC. 751 MILLER DR.,SE LEESBURG, VA 20175 US Other 510(k) Applications for this Company
Contact	NANCY GIEZEN Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OSH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/18/2013
Decision Date	08/30/2013
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