Orthofix, Inc. - FDA 510(k) Cleared Devices
57
Total
57
Cleared
0
Denied
Orthofix, Inc. has 57 FDA 510(k) cleared medical devices. Based in Mckinney, US.
Latest FDA clearance: May 2024. Active since 1996.
Browse the FDA 510(k) cleared devices submitted by Orthofix, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Orthofix, Inc.
6 devices
Cleared
May 28, 2024
PILLAR SA Ti Spacer System (82-XXX)
Orthopedic
70d
Cleared
Aug 31, 2021
CONSTRUX Mini PEEK Spacer System/CONSTRUX Mini PEEK VBR System, CONSTRUX Mini...
Orthopedic
89d
Cleared
Jul 30, 2021
Ascent POCT System, Centurion POCT System, Spinal Fixation System (SFS),...
Orthopedic
57d
Cleared
Mar 25, 2021
FIREBIRD SI Fusion System
Orthopedic
20d
Cleared
Mar 18, 2021
CONSTRUX Mini Ti Spacer System
Orthopedic
125d
Cleared
Mar 03, 2021
FORZA Ti Spacer System
Orthopedic
86d