MAUDE manufacturer profile
MSD BARTLETT MFG · MAX
MAUDE profile for Intervertebral Fusion Device With Bone Graft, Lumbar
Key facts
| Manufacturer | MSD BARTLETT MFG |
|---|---|
| Manufacturer group | MSD BARTLETT MFG |
| Product code | MAX |
| Product code name | Intervertebral Fusion Device With Bone Graft, Lumbar |
At a glance
- 10–99 MAUDE reports
- 1–9 Injury reports
- 10–99 Malfunction reports
- 1–9 Problems flagged by Orca1 signal analytics
- Break, No Known Impact Or Consequence To Patient, Detachment Of Device Component, Appropriate Term/Code Not Available, No Clinical Signs, Symptoms or Conditions, Perforation of Vessels, Blood Loss, Product Quality 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