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) | K173892 | NuVasive® XLX Interbody System | MAX | 2018-05-04 | View |
| 510(k) | K180198 | NuVasive® VuePoint® II OCT System | NKG | 2018-03-15 | View |
| 510(k) | K173025 | NuVasive® MLX® – Medial Lateral Expandable Lumbar Interbody System; NuVasive® AP Expandable XLIF System | MAX | 2018-02-08 | View |
| 510(k) | K172623 | NuVasive Navigation Instruments | OLO | 2017-12-21 | View |
| 510(k) | K172676 | NuVasive® Modulus-C Interbody System | ODP | 2017-12-14 | View |
| 510(k) | K173153 | Vertera Spine™ Coalesce™ Thoracolumbar Interbody Fusion System | MAX | 2017-12-06 | View |
| 510(k) | K172497 | NuVasive AttraX Scaffold | MQV | 2017-11-24 | View |
| 510(k) | K173030 | Vertera Spine Cohere Cervical Interbody Fusion Device | ODP | 2017-11-21 | View |
| 510(k) | K173314 | LessRay System | OWB | 2017-11-16 | View |
| 510(k) | K172979 | NuVasive® Growth Rod Conversion Set | PGM | 2017-11-06 | View |
| 510(k) | K172341 | NuVasive® Modulus TLIF Interbody System | MAX | 2017-10-26 | View |
| 510(k) | K172123 | NuVasive® Modulus XLIF Interbody System | MAX | 2017-10-11 | View |
| 510(k) | K171894 | NuVasive® Precept™ Spinal System | NKB | 2017-09-28 | View |
| 510(k) | K171633 | NuVasive TLX Interbody System | MAX | 2017-09-28 | View |
| 510(k) | K170800 | NuVasive LessRay with Enhanced Tracking | OWB | 2017-08-18 | View |
| 510(k) | K170962 | NuVasive® CoRoent® Thoracolumbar System | MAX | 2017-06-26 | View |
| 510(k) | K170961 | NuVasive CoRoent Small Interlock II System | OVE | 2017-06-08 | View |
| 510(k) | K163707 | NuVasive CoRoent Ti-C System | MAX | 2017-05-01 | View |
| 510(k) | K162647 | NuVasive NuvaLine Mobile App | LLZ | 2017-05-01 | View |
| 510(k) | K170592 | NuVasive BASE Interfixated Titanium System | OVD | 2017-04-26 | View |
No matching devices.
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