MAUDE manufacturer profile
AESCULAP AG · KWP
MAUDE profile for Appliance, Fixation, Spinal Interlaminal
Key facts
| Manufacturer | AESCULAP AG |
|---|---|
| Manufacturer group | AESCULAP AG |
| Product code | KWP |
| Product code name | Appliance, Fixation, Spinal Interlaminal |
At a glance
- 100–999 MAUDE reports
- 100–999 Injury reports
- 10–99 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Implant Pain, Device Appears to Trigger Rejection, Failure of Implant, Migration, Patient-Device Incompatibility, Insufficient Information, No Known Impact Or Consequence To Patient 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