Nu Vasive, Incorporated
FDA 510(k) & PMA Approved Devices — 79 products
Total Devices79
Categories18
Latest FDA decision2023-07-11
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K170271 | NuVasive(r) Monolith Corpectomy System | MQP | 2017-03-30 | View |
| 510(k) | K163491 | NuVasive CoRoent Small Interbody System | ODP | 2017-03-24 | View |
| 510(k) | K162313 | NuVasive Next Generation NVM5 System | PDQ | 2017-03-16 | View |
| 510(k) | K163230 | NuVasive Modulus XLIF Interbody System | MAX | 2017-03-16 | View |
| 510(k) | K170126 | NuVasive® Reline® 4.5-5.0 System | NKB | 2017-03-09 | View |
| 510(k) | K162138 | NuVasive CoRoent Small Ti-C System | ODP | 2016-10-26 | View |
| 510(k) | K161014 | NuVasive® Reline® System | NKB | 2016-09-28 | View |
| 510(k) | K161442 | NuVasive® CoRoent® Small Interlock™ System | OVE | 2016-09-28 | View |
| 510(k) | K161230 | NuVasive Lumbar Interbody Implants | MAX | 2016-08-25 | View |
| 510(k) | K161265 | NuVasive® VersaTie System | OWI | 2016-07-15 | View |
| 510(k) | K153105 | MLX™ - Medial Lateral Expandable Lumbar Interbody System | MAX | 2016-07-11 | View |
| 510(k) | K160916 | CoRoent® Ti-C System | MAX | 2016-06-28 | View |
| 510(k) | K160989 | NuVasive® Reline® System | NKB | 2016-06-09 | View |
| 510(k) | K160051 | NuVasive® Interfixated Interbody System | OVD | 2016-04-20 | View |
| 510(k) | K153419 | NuVasive CoRoent Thoracolumbar System | MAX | 2016-04-13 | View |
| 510(k) | K153782 | NuVasive® Lumbar Interbody Implants | MAX | 2016-03-24 | View |
| 510(k) | K153627 | NuVasive® TLX Interbody System | MAX | 2016-03-17 | View |
| 510(k) | K152942 | NuVasiveNVM5 System | PDQ | 2016-01-13 | View |
| 510(k) | K153336 | VuePoint OCT System | NKG | 2016-01-07 | View |
No matching devices.
Page 4 of 4