Phygen, LLC - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Phygen, LLC has 7 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 7 cleared submissions from 2011 to 2012. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Phygen, LLC Filter by specialty or product code using the sidebar.
7 devices
Cleared
Mar 07, 2012
LEUCADIA 4.5 MM PEDICLE SCREW SYSTEM
Orthopedic
30d
Cleared
Jan 17, 2012
LEUCADIA AUTOLOK PEDICLE SCREW SYSTEM
Orthopedic
63d
Cleared
Nov 02, 2011
LEUCADIA(TM) MIS PEDICLE SCREW SYSTEM
Orthopedic
30d
Cleared
Aug 02, 2011
DEL MAR MONOAXIAL PEDICLE SCREW SYSTEM
Orthopedic
145d
Cleared
May 25, 2011
LEUCADIA PEDICLE SCREW SYSTEM
Orthopedic
84d
Cleared
Mar 02, 2011
LAGUNA PEDICLE SCREW SYSTEM
Orthopedic
69d
Cleared
Feb 08, 2011
LEUCADIA PEDICLE SCREW SYSTEM
Orthopedic
111d