Trans1 Incorporated - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Trans1 Incorporated has 9 FDA 510(k) cleared medical devices. Based in Wilmington, US.
Historical record: 9 cleared submissions from 2005 to 2012. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Trans1 Incorporated Filter by specialty or product code using the sidebar.
9 devices
Cleared
Aug 23, 2012
TRANS1 INTERBODY FUSION SYSTEM
Orthopedic
143d
Cleared
Mar 14, 2011
TRANS1 AXIALIF PLUS
Orthopedic
209d
Cleared
Aug 26, 2010
TRANS1 LATERAL INTERVERTEBRAL FUSION DEVICE, T
Orthopedic
213d
Cleared
Jan 21, 2010
AXIALIF 2L, AXIALIF 2-LEVEL SYSTEM, AXIALIF APOLLO, AXIALIF II
Orthopedic
190d
Cleared
Apr 28, 2008
TRANS1 AXIALIF 2-LEVEL OR II SYSTEM
Orthopedic
124d
Cleared
Mar 11, 2008
TRANS1 FACET SCREW
Orthopedic
88d
Cleared
Jan 11, 2008
TRANS1 AXIAL FIXATON SYSTEM
Orthopedic
28d
Cleared
Sep 26, 2005
TRANS1 FACET SCREWS
Orthopedic
80d
Cleared
Jun 14, 2005
TRANS1 AXIALIF SYSTEM
Orthopedic
57d