Medartis, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K232324 | StealthFix Intraosseous Fixation System | JDR | 2023-08-30 | View |
| 510(k) | K052061 | MODUS IMF SCREWS 2.0 | DZE | 2005-10-21 | View |
| 510(k) | K051567 | APTUS TITANIUM OSTEOSYNTHESIS SYSTEM | HRS | 2005-08-23 | View |
| 510(k) | K051946 | MODUS MODULAR DISTRACTION OSTEOGENESIS SYSTEM | MQN | 2005-08-22 | View |
| 510(k) | K050934 | MODUS TITANIUM OSTEOSYNTHESIS SYSTEM | JEY | 2005-05-05 | View |
No matching devices.
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