MAUDE manufacturer profile
AESCULAP AG · KWQ
MAUDE profile for Appliance, Fixation, Spinal Intervertebral Body
Key facts
| Manufacturer | AESCULAP AG |
|---|---|
| Manufacturer group | AESCULAP AG |
| Product code | KWQ |
| Product code name | Appliance, Fixation, Spinal Intervertebral Body |
At a glance
- 100–999 MAUDE reports
- 100–999 Injury reports
- 10–99 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Failure of Implant, Implant Pain, Pain, No Clinical Signs, Symptoms or Conditions, Insufficient Information, Biocompatibility, Patient-Device Incompatibility, Device Appears to Trigger Rejection 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