Renovis Surgical Technologies
FDA 510(k) & PMA Approved Devices — 6 products
Total Devices6
Categories5
Latest Approval2019-06-20
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K190122 | Renovis A200 PS Knee System as part of the Renovis A200 Knee System | JWH | 2019-06-20 | View |
| 510(k) | K182007 | Renovis Tesera C/Tesera SC Anterior Cervical Fusion (ACF) System | OVD | 2018-12-07 | View |
| 510(k) | K181655 | Renovis S180 Lateral Lumbar Interbody Fusion System | MAX | 2018-09-11 | View |
| 510(k) | K171543 | Renovis Surgical Hip Replacement System | OQG | 2017-11-16 | View |
| 510(k) | K170888 | Renovis S141 Lumbar Interbody Fusion System | MAX | 2017-08-08 | View |
| 510(k) | K153250 | Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System | OVE | 2016-03-16 | View |
No matching devices.