FDA 510(k) Application Details - K180851

Device Classification Name	Orthosis, Cervical Pedicle Screw Spinal Fixation   More FDA Info for this Device
510(K) Number	K180851
Device Name	Orthosis, Cervical Pedicle Screw Spinal Fixation
Applicant	Medtronic Sofamor Danek USA, Inc 1800 Pyramid Place Memphis, TN 38132 US Other 510(k) Applications for this Company
Contact	Ankit K Shah 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	04/02/2018
Decision Date	04/18/2018
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