Medtronic Sofamor Danek - FDA 510(k) Cleared Devices
154
Total
147
Cleared
0
Denied
Medtronic Sofamor Danek has 147 FDA 510(k) cleared orthopedic devices. Based in Memphis, US.
Last cleared in 2021. Active since 2002.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Medtronic Sofamor Danek
154 devices
Cleared
Dec 13, 2021
Centerpiece Plate Fixation System
Orthopedic
131d
Cleared
Aug 26, 2020
Adaptix Interbody System with Titan nanoLOCK Surface Technology
Orthopedic
106d
Cleared
Dec 20, 2017
T2 STRATOSPHERE™ Expandable Corpectomy System
Orthopedic
82d
Cleared
Sep 19, 2017
ELEVATE Spinal System, CAPSTONE PTC Spinal System, CRESCENT Spinal System,...
Orthopedic
60d
Cleared
Jul 06, 2017
CRESCENT™ Spinal System
Orthopedic
91d
Cleared
Jun 13, 2017
FUSE Spinal System
Orthopedic
26d
Cleared
May 11, 2017
CD HORIZON® Spinal System, Medtronic Reusable Instruments for Use with the...
Orthopedic
66d
Cleared
Aug 12, 2016
RIALTO(TM) SI Fusion System, Medtronic Reusable Instruments for Use with the...
Orthopedic
106d
Cleared
Jan 19, 2016
CORNERSTONE PSR Cervical Fusion System, PERIMETER C Spinal System, PEEK...
Orthopedic
57d
Cleared
Mar 13, 2014
CD HORIZON SPINAL SYSTEM
Orthopedic
38d
Cleared
Nov 16, 2012
CD HORIZON SPIRE Z SPINAL SYSTEM
Orthopedic
30d
Cleared
Jul 26, 2012
SOVEREIGN SPINAL SYSTEM
Orthopedic
20d
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