Nanovis, LLC
FDA 510(k) & PMA Approved Devices — 7 products
Total Devices7
Categories3
Latest Approval2024-09-05
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K241605 | Adaptix PEEK Interbody System with Nanotechnology; Capstone Control PEEK Spinal System with Nanotechnology | MAX | 2024-09-05 | View |
| 510(k) | K230936 | Anatomic PEEK Cervical Fusion System with Nanotechnology | ODP | 2023-06-02 | View |
| 510(k) | K203452 | Nano FortiFix® System | NKB | 2020-12-22 | View |
| 510(k) | K191822 | Nano FortiCore, FortiCore | ODP | 2019-10-11 | View |
| 510(k) | K171312 | FortiCore® | MAX | 2018-01-22 | View |
| 510(k) | K161485 | Nanovis Intervertebral Body Fusion System and Forticore(R) | MAX | 2016-09-06 | View |
| 510(k) | K160874 | Nanovis Intervertebral Body Fusion System and FortiCore® | MAX | 2016-06-28 | View |
No matching devices.