FDA Adverse Event
Other
Summary report: N
*
MDR report key: 665721
·
Received December 22, 2005
Report
- Report Number
- 1030489-2005-00377
- Event Type
- Other
- Date Received
- December 22, 2005
- Report Date
- November 22, 2005
- Manufacturer
- WARSAW ORTHOPEDIC INC.
- Product Code
- FSM
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | * | IMPLANT/INSTRUMENT CASE | FSM | WARSAW ORTHOPEDIC INC. | NA | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |