MAUDE manufacturer profile
AESCULAP IMPLANT SYSTEMS · MJO
MAUDE profile for Prosthesis, Intervertebral Disc
Key facts
| Manufacturer | AESCULAP IMPLANT SYSTEMS |
|---|---|
| Manufacturer group | AESCULAP AG |
| Product code | MJO |
| Product code name | Prosthesis, Intervertebral Disc |
At a glance
- 10–99 MAUDE reports
- 1–9 Injury reports
- 10–99 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Migration or Expulsion of Device, No Code Available, Neurological Deficit/Dysfunction, Weakness, Loss of Range of Motion, Adverse Event Without Identified Device or Use Problem, Numbness, Pain 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