MAUDE MDR 9813306
- MDR report key
- 9813306
- Report number
- 0009613350-2020-00105
- Event key
- 0
- Event type
- 3
- Date of event
- 2019-08-23
- Date received
- 2020-03-10
- Adverse event
- 3
- Product problem
- 3
- Patients in event
- 0
- Reporter occupation
- 0
- Health professional
- 0
- Initial report to FDA
- 0
- Event location
- 3
Devices#
Seq, Brand, Generic table| Seq | Brand | Generic | Manufacturer | Product code | Model | Catalog | Lot | PMA | 510(k) | Implant | Evaluated | Availability |
|---|
| 1 | DUROM | N/A | ZIMMER GMBH | KXA | N/A | UNKNOWN | UNKNOWN | | | | R
| N |
Patients#
Sequence, Received, Treatment table| Sequence | Received | Treatment | Outcome |
|---|
| 1 | 2020-03-10 | 0 | 1. H; 2. R
|
Event Narratives#
No narrative records found.