Allez Spine, LLC - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Allez Spine, LLC has 7 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 7 cleared submissions from 2005 to 2009. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Allez Spine, LLC Filter by specialty or product code using the sidebar.
7 devices
Cleared
Aug 07, 2009
LAGUNA SIZE 8 PEDICLE SCREW SYSTEM
Orthopedic
36d
Cleared
Jul 09, 2009
DEL MAR MONOAXIAL PEDICLE SCREW SYSTEM
Orthopedic
73d
Cleared
Jan 22, 2009
LAGUNA POLYAXIAL PEDICLE SCREW SYSTEM
Orthopedic
30d
Cleared
Jul 02, 2008
LAGUNA SIZE 8 PEDICLE SCREW
Orthopedic
285d
Cleared
Jun 11, 2007
ALLEZ SPINE CROSS CONNECTORS
Orthopedic
115d
Cleared
Dec 09, 2005
LAGUNA MONOAXIAL PEDICLE SCREW SYSTEM
Orthopedic
206d
Cleared
May 04, 2005
LAGUNA PEDICLE SCREW SYSTEM
Orthopedic
113d