Wrightmedicaltechnologyinc
FDA 510(k) & PMA Approved Devices — 37 products
Total Devices37
Categories8
Latest FDA decision2023-01-27
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K222835 | Prophecy Preoperative Navigation Alignment System | HSN | 2023-01-27 | View |
| 510(k) | K213342 | PRO-DENSE LoVisc Bone Graft Substitute | MQV | 2022-01-05 | View |
| 510(k) | K212996 | Sterile PHALINX Hammertoe System | HWC | 2021-11-16 | View |
| 510(k) | K202815 | PROPHECY Preoperative Navigation Alignment System | HSN | 2021-03-10 | View |
| 510(k) | K201259 | ORTHOLOC 2 with 3Di Technology Pilon Fracture Plating System | HRS | 2021-01-08 | View |
| 510(k) | K200507 | PRO-DENSE LoVisc Bone Graft Substitute | MQV | 2020-10-21 | View |
| 510(k) | K193067 | The INBONE™ Total Ankle System, the INFINITY™ Total Ankle System and the INVISION™ Total Ankle Revision System | HSN | 2020-06-08 | View |
| 510(k) | K191393 | INFINITY Total Ankle System, INBONE Total Ankle System | HSN | 2019-08-22 | View |
| 510(k) | K190970 | PROSTEP™ TBI™ (Tailors Bunion Implant) System | HWC | 2019-08-13 | View |
| 510(k) | K183620 | PROSTEP TBC Implant System | HRS | 2019-06-06 | View |
| 510(k) | K190482 | IGNITE Bone Void Filler | MQV | 2019-05-28 | View |
| 510(k) | K190670 | ORTHOLOC™ 2 Lapidus with Rotation System | HRS | 2019-05-14 | View |
| 510(k) | K190283 | PROSTIM Injectable Inductive Graft | MQV | 2019-03-14 | View |
| 510(k) | K183026 | Wright Jones Fracture System | HWC | 2019-03-13 | View |
| 510(k) | K181377 | PROSTEP MICA Screw System | HWC | 2019-01-11 | View |
| 510(k) | K182823 | PRODENSE Bone Graft Substitute | MQV | 2018-11-02 | View |
| 510(k) | K181255 | PRODENSE Bone Graft Substitute | MQV | 2018-09-12 | View |
| 510(k) | K181557 | INFINITY Total Ankle System | HSN | 2018-08-09 | View |
| 510(k) | K180024 | SALVATION Midfoot Nail | HWC | 2018-07-11 | View |
| 510(k) | K180730 | INVISION Total Ankle Revision System | HSN | 2018-07-11 | View |
No matching devices.
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