Rti Surgical, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
Total Devices5
Categories4
Latest Approval2025-10-22
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K253145 | Pre-Sutured Tendon | GAT | 2025-10-22 | View |
| 510(k) | K241555 | Moldable Bone Void Filler and Moldable Bone Void Filler + CCC | MQV | 2025-02-21 | View |
| 510(k) | K230036 | Pre-Sutured Tendon (4561SC / Single Strand); Pre-Sutured Tendon (4564SC / Quadruple Strand ) | GAT | 2023-06-23 | View |
| 510(k) | K172343 | Fortilink® Interbody Fusion (IBF) System with TETRAfuse® 3D Technology | MAX | 2017-10-23 | View |
| 510(k) | K163673 | Fortilink-C with TETRAfuse 3D Technology | ODP | 2017-05-23 | View |
No matching devices.