FDA Adverse Event
Injury
Summary report: N
SUPERIOR END PLATE MEDIUM 6°-STERILE
MDR report key: 2944844
·
Received February 5, 2013
Report
- Report Number
- 2530088-2013-00103
- Event Type
- Injury
- Date Received
- February 5, 2013
- Date of Event
- January 1, 2010
- Report Date
- April 3, 2024
- Manufacturer
- BRANDYWINE
- Product Code
- MJO
- UDI-DI
- 10705034700175
- PMA / PMN Number
- P050010
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 49530 | SUPERIOR END PLATE MEDIUM 6°-STERILE | PROSTHESIS, INTERVERTEBRAL DISC | MJO | BRANDYWINE | 5372894 | 10705034700175 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown | Required Intervention |