FDA Adverse Event
Other
Summary report: N
DURAMATRIX
MDR report key: 1864585
·
Received September 7, 2010
Report
- Report Number
- 2249852-2010-00001
- Event Type
- Other
- Date Received
- September 7, 2010
- Date of Event
- July 2, 2010
- Report Date
- September 27, 2010
- Manufacturer
- COLLAGEN MATRIX, INC.
- Product Code
- GXQ
- PMA / PMN Number
- K040888
- Report Source
- Manufacturer report
- Reporter Location
- NJ, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
PT REQUIRED REVISION SURGERY DUE TO CSF LEAKAGE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | DURAMATRIX | COLLAGEN DURA SUBSTITUTE MEMBRANE | GXQ | COLLAGEN MATRIX, INC. | CDSM33 | 0904101022 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |