MAUDE report
MAUDE report 37476: INTERPORE IMZ IMPLANT
Injury · received Sep 6, 1996 · INTERPORE INTERNATIONAL
Key facts
| MDR report key | 37476 |
|---|---|
| Report number | 2029012-1996-00003 |
| Event type | Injury |
| Brand name | INTERPORE IMZ IMPLANT |
| Catalog number | UNK |
| Manufacturer | INTERPORE INTERNATIONAL |
| Product code | DZE |
| Device class | Class II |
| Date received by FDA | Sep 6, 1996 |
| Report date | Sep 5, 1996 |
| Report source | Maude |
At a glance
- None Device problems coded
- No 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: