Citieffe S.R.L.
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K250197 | Estremo Fibular Nail | HSB | 2025-10-17 | View |
| 510(k) | K183666 | EBA One Nailing System | HSB | 2019-11-14 | View |
| 510(k) | K181540 | Estremo Citieffe Nailing System | HSB | 2019-01-16 | View |
| 510(k) | K180150 | PL8 Wrist Reconstruction Plate | HRS | 2018-08-02 | View |
| 510(k) | K163323 | Dolphix® External Fixation System MR Conditional | KTT | 2017-03-20 | View |
| 510(k) | K131005 | EBA2 FEMORAL NAILING SYSTEM | HSB | 2013-06-25 | View |
No matching devices.
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