Medical Device Manufacturer · CA , Montreal

Co-Ligne AG - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2004

Recent clearances: GII SPINAL FIXATION SYSTEM, GII-TI-POLY AXIAL SCREW, OSTAPEK VBR SYSTEM, GII SPINAL FIXATION SYSTEM

View 4 510(k) Devices ↓
4
Total
4
Cleared
0
Denied

FDA 510(k) Regulatory Record - Co-Ligne AG Orthopedic ✕

4 devices
1-4 of 4
Cleared Sep 14, 2009
GII SPINAL FIXATION SYSTEM, GII-TI-POLY AXIAL SCREW
K083567 · MNH
Orthopedic · 285d
Cleared Jun 24, 2008
OSTAPEK VBR SYSTEM
K072326 · MQP
Orthopedic · 309d
Cleared Oct 26, 2005
GII SPINAL FIXATION SYSTEM
K051089 · MNH
Orthopedic · 181d
Cleared Jan 20, 2004
GII SPINAL FIXATION SYSTEM
K032604 · MNH
Orthopedic · 148d
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