Medtronic Sofamor Danek USA - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
FDA 510(k) cleared devices by Medtronic Sofamor Danek USA Orthopedic ✕
9 devices
Cleared
Apr 12, 2022
Anteralign Spinal System with Titan nanoLOCK Surface Technology
Orthopedic
111d
Cleared
Apr 04, 2017
CD HORIZON™ Fenestrated Screw Set
Orthopedic
60d
Cleared
Feb 25, 2014
CD HORIZON SPINAL SYSTEM GROWTH ROD SET
Orthopedic
67d
Cleared
Aug 06, 2013
CD HORIZON SPINAL SYSTEM
Orthopedic
28d
Cleared
Jun 05, 2013
CD HORIZON SPINAL SYSTEM
Orthopedic
28d
Cleared
Apr 09, 2013
CAPSTONE L SPINAL SYSTEM
Orthopedic
104d
Cleared
Feb 06, 2012
PERIMETER INTERBODY FUSION DEVICE
Orthopedic
56d
Cleared
Nov 09, 2011
TELAMON PEEK SPINAL SYSTEM
Orthopedic
254d
Cleared
Oct 12, 2011
CORNERSTONE (R) PSR CERVICAL FUSION SYSTEM
Orthopedic
161d