FDA 510(k) Application Details - K171250

Device Classification Name	Orthosis, Cervical Pedicle Screw Spinal Fixation   More FDA Info for this Device
510(K) Number	K171250
Device Name	Orthosis, Cervical Pedicle Screw Spinal Fixation
Applicant	Astura Medical 3186 Lionshead Ave, Suite 100 Carlsbad, CA 92010 US Other 510(k) Applications for this Company
Contact	Troy Taylor Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	NKG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/28/2017
Decision Date	10/02/2017
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