MAUDE manufacturer profile
AMPLIFY SURGICAL · MAX
MAUDE profile for Intervertebral Fusion Device With Bone Graft, Lumbar
Key facts
| Manufacturer | AMPLIFY SURGICAL |
|---|---|
| Manufacturer group | AMPLIFY SURGICAL |
| Product code | MAX |
| Product code name | Intervertebral Fusion Device With Bone Graft, Lumbar |
At a glance
- 1–9 MAUDE reports
- 1–9 Injury reports
- 1–9 Malfunction reports
- 1–9 Problems flagged by Orca1 signal analytics
- Insufficient Information, Device Markings/Labelling Problem, Improper or Incorrect Procedure or Method, Loosening of Implant Not Related to Bone-Ingrowth, Fracture, Implant Pain, Material Integrity Problem 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