Co-Ligne AG
4 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| GII SPINAL FIXATION SYSTEM, GII-TI-POLY AXIAL SCREW (K083567) | Co-Ligne AG | 2009-09-14 |
| OSTAPEK VBR SYSTEM (K072326) | Co-Ligne AG | 2008-06-24 |
| GII SPINAL FIXATION SYSTEM (K051089) | Co-Ligne AG | 2005-10-26 |
| GII SPINAL FIXATION SYSTEM (K032604) | Co-Ligne AG | 2004-01-20 |
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Every clearance here is in the API, with alerts when new ones post.