Medical Device Manufacturer · US , Lweisville , TX

Orthofix - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2012
3
Total
3
Cleared
0
Denied

Orthofix has 3 FDA 510(k) cleared medical devices. Based in Lweisville, US.

Historical record: 3 cleared submissions from 2012 to 2013. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Orthofix Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Orthofix

3 devices
1-3 of 3
Cleared Mar 28, 2013
FIREBIRD SPINAL FIXATION SYSTEM
K130176 · NKB
Orthopedic · 62d
Cleared Dec 03, 2012
FIREBIRD SPINAL FIXATION SYSTEM, PHOENIX MIS SPINAL FIXATION SYSTEM
K122901 · NKB
Orthopedic · 73d
Cleared Nov 29, 2012
CONSTRUX MINI PEEK TI SPACER SYSTEM
K121649 · ODP
Orthopedic · 177d
Filters
Filter by Specialty
All3 Orthopedic 3