MAUDE manufacturer profile
GLOBUS MEDICAL, INC. · MAX
MAUDE profile for Intervertebral Fusion Device With Bone Graft, Lumbar
Key facts
| Manufacturer | GLOBUS MEDICAL, INC. |
|---|---|
| Manufacturer group | GLOBUS MEDICAL, INC. |
| Product code | MAX |
| Product code name | Intervertebral Fusion Device With Bone Graft, Lumbar |
At a glance
- 100–999 MAUDE reports
- 1–9 Death reports
- 10–99 Injury reports
- 10–99 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Insufficient Information, Failure of Implant, Migration, No Clinical Signs, Symptoms or Conditions, Migration or Expulsion of Device, Foreign Body In Patient, Break 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