MAUDE manufacturer profile
NUVASIVE, INCORPORATED · MAX
MAUDE profile for Intervertebral Fusion Device With Bone Graft, Lumbar
Key facts
| Manufacturer | NUVASIVE, INCORPORATED |
|---|---|
| Manufacturer group | NUVASIVE, INCORPORATED |
| Product code | MAX |
| Product code name | Intervertebral Fusion Device With Bone Graft, Lumbar |
At a glance
- 100–999 MAUDE reports
- 1–9 Death reports
- 100–999 Injury reports
- 100–999 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Adverse Event Without Identified Device or Use Problem, Fracture, No Clinical Signs, Symptoms or Conditions, Pain, Failure of Implant, Migration or Expulsion of Device, Migration, Foreign Body In Patient Most reported problems
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About MAUDE manufacturer and product code profiles
Manufacturer profiles aggregate MAUDE reports for one manufacturer within one product code, the level at which device safety signals are usually reviewed.
Source: U.S. Food and Drug Administration (FDA), MAUDE database; aggregation by Orca1