FDA 510(k) Applications Submitted by CO-LIGNE AG
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K032604 | 08/25/2003 | GII SPINAL FIXATION SYSTEM | CO-LIGNE AG |
| K072326 | 08/20/2007 | OSTAPEK VBR SYSTEM | CO-LIGNE AG |
| K051089 | 04/28/2005 | GII SPINAL FIXATION SYSTEM | CO-LIGNE AG |
| K083567 | 12/03/2008 | GII SPINAL FIXATION SYSTEM, GII-TI-POLY AXIAL SCREW | CO-LIGNE AG |
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