FDA 510(k) Application Details - K160702

Device Classification Name	Appliance, Fixation, Spinal Intervertebral Body   More FDA Info for this Device
510(K) Number	K160702
Device Name	Appliance, Fixation, Spinal Intervertebral Body
Applicant	Astura Medical 5670 El Camino Real, Suite B Carlsbad, CA 92008 US Other 510(k) Applications for this Company
Contact	TROY TAYLOR Other 510(k) Applications for this Contact
Regulation Number	888.3060   More FDA Info for this Regulation Number
Classification Product Code	KWQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/14/2016
Decision Date	08/23/2016
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