FDA Adverse Event
Injury
Summary report: N
2110898-1997-00020
MDR report key: 105934
·
Received July 15, 1997
Report
- Report Number
- 2110898-1997-00020
- Event Type
- Injury
- Date Received
- July 15, 1997
- Date of Event
- January 1, 1980
- Manufacturer
- 3M COMPANY
- Product Code
- FTR
- Removal / Correction Number
- UNK
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | Implant | FTR | 3M COMPANY | UNK | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |