FDA Adverse Event
Injury
Summary report: N
*
MDR report key: 866824
·
Received June 6, 2007
Report
- Report Number
- 9612771-2007-00032
- Event Type
- Injury
- Date Received
- June 6, 2007
- Manufacturer
- PLUS ORTHOPEDICS AG
- Product Code
- ---
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
THERE ARE NO INDICATIONS THAT THE DEVICE HAS BEEN RETURNED TO THE MFR. SHOULD THE DEVICE BE RETURNED TO THE MFR, THEN AN EVAL WILL BE PERFORMED AT THAT TIME.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | * | --- | PLUS ORTHOPEDICS AG |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |