MAUDE report
MAUDE report 40266: TRACKER DRILL BIT
Injury · received Sep 26, 1996 · DEPUY, INC.
Key facts
| MDR report key | 40266 |
|---|---|
| Report number | 1818910-1996-00015 |
| Event type | Injury |
| Brand name | TRACKER DRILL BIT |
| Model number | 1NA |
| Catalog number | 2954-20-000 |
| Manufacturer | DEPUY, INC. |
| Product code | HTW |
| Device class | Class I |
| PMA or 510(k) number | Device Exempt |
| Date received by FDA | Sep 26, 1996 |
| Report date | Aug 28, 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: