Synovis Life Technologies. Inc. (A Subsidiary of Baxter
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest Approval2021-10-27
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K213125 | PERI-STRIPS Dry Staple Line Reinforcement with VERITAS Collagen Matrix with SECURE GRIP Technology | FTM | 2021-10-27 | View |
No matching devices.