FDA Adverse Event
Injury
Summary report: N
2182207-1997-00122
MDR report key: 83423
·
Received April 11, 1997
Report
- Report Number
- 2182207-1997-00122
- Event Type
- Injury
- Date Received
- April 11, 1997
- Manufacturer
- MEDTRONIC INC.
- Product Code
- LKK
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | Implant | LKK | MEDTRONIC INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |