MAUDE manufacturer profile
ARTHREX, INC. · QHQ
MAUDE profile for Total Shoulder Arthroplasty System
Key facts
| Manufacturer | ARTHREX, INC. |
|---|---|
| Manufacturer group | ARTHREX, INC. |
| Product code | QHQ |
| Product code name | Total Shoulder Arthroplasty System |
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, Pain, Patient Device Interaction Problem, Loosening of Implant Not Related to Bone-Ingrowth, Adverse Event Without Identified Device or Use Problem, Insufficient Information, Break, Appropriate Term/Code Not Available 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