FDA Adverse Event
Injury
Summary report: N
9612771-2006-00021
MDR report key: 763190
·
Received September 1, 2006
Report
- Report Number
- 9612771-2006-00021
- Event Type
- Injury
- Date Received
- September 1, 2006
- Product Code
- KWB
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
THE EXPLANTED DEVICE WAS NOT RETURNED TO PLUS ORTHOPEDICS SO AN EVAL CANNOT BE PERFORMED. THE SURGEON HAS INDICATED TO PLUS ORTHOPEDICS USA THAT HE DOES NOT BELIEVE PLUS PRODUCTS CAUSED OR CONTRIBUTED TO THE PT'S CONDITION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | KWB |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |