Xtremi-T, LLC
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K050388 | REFIX INTERNAL FRACTURE FIXATION SCREWS | HWC | 2005-09-07 | View |
| 510(k) | K043339 | REFIX PIN (PLLA), MODELS 2070L, 2770L, 3570L, 4570L; (PLGA), MODELS 2070LG, 2770LG, 3570LG, 4570LG | HTY | 2005-04-18 | View |
No matching devices.
Advertisement