Signus Medical, LLC - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Signus Medical, LLC has 6 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 6 cleared submissions from 2002 to 2008. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Signus Medical, LLC Filter by specialty or product code using the sidebar.
6 devices
Cleared
Jul 14, 2008
MONOPOLY PEDICLE SCREW SYSTEM
Orthopedic
87d
Cleared
Aug 16, 2005
NUBIC SPINAL IMPLANT
Orthopedic
13d
Cleared
Oct 22, 2003
CONKLUSION PEDICLE SCREW SYSTEM
Orthopedic
168d
Cleared
Jul 30, 2003
PEEK TETRIS SPINAL IMPLANT
Orthopedic
54d
Cleared
Apr 08, 2003
TETRIS SPINAL IMPLANT
Orthopedic
228d
Cleared
Jun 11, 2002
RABEA CEMENT RESTRICTOR
Orthopedic
89d