Nexa Orthopedics, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Nexa Orthopedics, Inc. has 16 FDA 510(k) cleared orthopedic devices. Based in Vista, US.
Historical record: 16 cleared submissions from 1997 to 2007.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
16 devices
Cleared
Nov 08, 2007
NEXFIX COMPRESSION PIN
Orthopedic
44d
Cleared
Jul 20, 2007
NEXA ORTHOPEDICS TOTAL SHOULDER SYSTEM
Orthopedic
87d
Cleared
May 18, 2007
NEXFIX COMPRESSION STAPLE
Orthopedic
67d
Cleared
May 10, 2006
NEXA CARPO METACARPAL IMPLANT
Orthopedic
85d
Cleared
Jan 26, 2006
NEXA COMPRESSION SCREW
Orthopedic
17d
Cleared
Dec 22, 2005
NEXA BONE PLATE AND SCREW SYSTEM
Orthopedic
15d
Cleared
Dec 14, 2005
NEXA BONE SCREW SYSTEM
Orthopedic
8d
Cleared
Sep 06, 2005
TAPERED COMPRESSION PIN
Orthopedic
70d
Cleared
Aug 01, 2005
OSTEOCURE RESORBABLE BEAD KIT
Orthopedic
62d
Cleared
Dec 23, 2003
SUBTALAR PEG IMPLANT
Orthopedic
85d
Cleared
Dec 15, 2003
SUBTALAR ARTHRORISIS IMPLANT
Orthopedic
89d
Cleared
Jan 17, 2003
LESSER METATARSAL PHALANGEAL JOINT IMPLANT
Orthopedic
88d