FDA Adverse Event
Other
Summary report: N
MAYO CLINIC CONGRUENT BONE PLATE SYSTEM
MDR report key: 655349
·
Received December 20, 2005
Report
- Report Number
- 3025141-2005-00012
- Event Type
- Other
- Date Received
- December 20, 2005
- Report Date
- December 1, 2005
- Manufacturer
- ACUMED
- Product Code
- HRS
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OH, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
SECOND SURGERY REQUIRED TO REPLACE BROKEN PLATE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MAYO CLINIC CONGRUENT BONE PLATE SYSTEM | BONE PLATE | HRS | ACUMED | PL-ELOM | W13451 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | Other |