MAUDE report
MAUDE report 8467: SIMON NITIINOL VENA CAVA FILTER
Injury · received Jan 24, 1994 · NITINOL MEDICAL TECHNOLOGIES, INC.
Key facts
| MDR report key | 8467 |
|---|---|
| Report number | 1018233-1993-00046 |
| Event type | Injury |
| Brand name | SIMON NITIINOL VENA CAVA FILTER |
| Catalog number | 2110F |
| Manufacturer | NITINOL MEDICAL TECHNOLOGIES, INC. |
| Product code | DTK |
| Device class | Class II |
| Date received by FDA | Jan 24, 1994 |
| Report date | Nov 29, 1993 |
| Report source | Maude |
At a glance
- None Device problems coded
- Yes Adverse event flagged
- No 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: