FDA Adverse Event
Malfunction
Summary report: N
6000030-1997-00238
MDR report key: 117162
·
Received August 29, 1997
Report
- Report Number
- 6000030-1997-00238
- Event Type
- Malfunction
- Date Received
- August 29, 1997
- Date of Event
- July 10, 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 |