MAUDE manufacturer profile
AESCULAP AG · OOG
MAUDE profile for Knee Arthroplasty Implantation System
Key facts
| Manufacturer | AESCULAP AG |
|---|---|
| Manufacturer group | AESCULAP AG |
| Product code | OOG |
| Product code name | Knee Arthroplasty Implantation System |
At a glance
- 100–999 MAUDE reports
- 100–999 Injury reports
- 10–99 Problems flagged by Orca1 signal analytics
- Failure of Implant, Patient-Device Incompatibility, Loosening of Implant Not Related to Bone-Ingrowth, Pain, Unspecified Infection, Patient Device Interaction Problem, Limited Mobility Of The Implanted Joint, Patient Problem/Medical 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