Suzhou Endophix Co., Ltd.
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories1
Latest FDA decision2024-05-03
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K232941 | Megaloop Button System | MBI | 2024-05-03 | View |
| 510(k) | K232725 | Javelot Ti Suture Anchor, Javelot Ti-D Suture Anchor | MBI | 2023-11-02 | View |
| 510(k) | K231002 | Javelot PK-S suture anchor, Javelot PK-S suture anchor (Knotless), Javelot PK-P suture anchor, Javelot PK-P suture anchor (Knotless), Javelot PK-L suture anchor (Knotless) | MBI | 2023-06-07 | View |
| 510(k) | K230874 | Syntheface PEEK Interference Screw, Syntheface PEEK Screw Sheath | MBI | 2023-05-23 | View |
No matching devices.