MAUDE report
MAUDE report 3898: KIRSCHNER REPLACEMENT RT. KNEE
Injury · received Feb 19, 1993 · KIRSCHNER MEDICAL CORPORATION
Key facts
| MDR report key | 3898 |
|---|---|
| Report number | 3898 |
| Event type | Injury |
| Brand name | KIRSCHNER REPLACEMENT RT. KNEE |
| Model number | UNKNOWN |
| Catalog number | UNKNOWN |
| Manufacturer | KIRSCHNER MEDICAL CORPORATION |
| Product code | ISY |
| Device class | Class I |
| PMA or 510(k) number | Device Exempt |
| Date received by FDA | Feb 19, 1993 |
| Report date | Dec 18, 1992 |
| Report source | Maude |
At a glance
- None Device problems coded
- 100–999 MAUDE reports for this product code
- 1–9 MAUDE reports for this brand
- None Death reports for this brand
- 1–9 Injury reports for this brand
- 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: