MAUDE report
MAUDE report 13942: STEFFEE PLATE
Injury · received Jun 13, 1994 · ACROMED CORP.
Key facts
| MDR report key | 13942 |
|---|---|
| Report number | MW1002438 |
| Event type | Injury |
| Brand name | STEFFEE PLATE |
| Model number | UNKNOWN |
| Catalog number | UNKNOWN |
| Manufacturer | ACROMED CORP. |
| Product code | MCV |
| Device class | Class III |
| Date received by FDA | Jun 13, 1994 |
| Report source | Maude |
At a glance
- None Device problems coded
- Yes Adverse event flagged
- Yes Product problem flagged
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About MAUDE medical device reports
MAUDE holds medical device reports (MDRs) of suspected device-associated deaths, serious injuries and malfunctions submitted to the FDA by manufacturers, importers, user facilities and the public. A report alone does not establish that a device caused an event.
Source: U.S. Food and Drug Administration (FDA), MAUDE (Manufacturer and User Facility Device Experience) database · Source date: