Medos International Sàrl
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories4
Latest FDA decision2023-09-29
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K231527 | TriALTIS Navigation Enabled Instruments | OLO | 2023-09-29 | View |
| 510(k) | K223688 | CONDUIT™ Lateral Lumbar Intervertebral Fusion Cage, CONDUIT™ Instruments | MAX | 2023-03-08 | View |
| 510(k) | K200245 | EXPEDIUM® Spine System; EXPEDIUM VERSE® Spine System | NKB | 2020-04-24 | View |
| 510(k) | K160879 | CONFIDENCE™ High Viscosity Spinal Cement, VIPER® and EXPEDIUM® Fenestrated Screw Systems | PML | 2016-12-20 | View |
No matching devices.