Medtronic Sofamor Danek, Inc. - FDA 510(k) Cleared Devices
99
Total
89
Cleared
0
Denied
Medtronic Sofamor Danek, Inc. has 89 FDA 510(k) cleared orthopedic devices. Based in Memphis, US.
Latest FDA clearance: Jun 2025. Active since 2000.
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, Inc.
99 devices
Cleared
Jun 12, 2025
Grafton™ DBM
Orthopedic
56d
Cleared
Jan 17, 2025
Mastergraft Matrix EXT
Orthopedic
49d
Cleared
Jul 18, 2023
Robotic Graft Delivery Instruments
Orthopedic
125d
Cleared
Sep 05, 2014
MASTERGRAFT MATRIX EXT
Orthopedic
60d
Cleared
Jul 09, 2014
DIVERGENCE MINI-PLATE ANTERIOR CERVICAL FUSION SYSTEM
Orthopedic
141d
Cleared
Mar 25, 2014
CD HORIZON SPINAL SYSTEM
Orthopedic
29d
Cleared
Dec 11, 2013
CLYDESDALE SPINAL SYSTEM
Orthopedic
86d
Cleared
Nov 22, 2013
CRESCENT SPINAL SYSTEM
Orthopedic
35d
Cleared
Sep 26, 2013
PERIMETER INTERBODY FUSION DEVICE
Orthopedic
28d
Cleared
Sep 23, 2013
T2 XVBR SPINAL SYSTEM, T2 ALTITUDE EXPANDABLE CORPECTOMY DEVICE
Orthopedic
90d
Cleared
Jul 25, 2013
CAPSTONE(R) SPINAL SYSTEM
Orthopedic
300d
Cleared
Mar 22, 2013
ANATOMIC PEEK CERVICAL FUSION SYSTEM CORNERSTONE PSR CERVICAL FUSION SYSTEM...
Orthopedic
254d
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