FDA Adverse Event
Injury
Summary report: N
2182207-2009-07623
MDR report key: 23776590
·
Received March 11, 2009
Report
- Report Number
- 2182207-2009-07623
- Event Type
- Injury
- Date Received
- March 11, 2009
- Date of Event
- February 16, 2009
- Report Date
- March 11, 2009
- Manufacturer
- MEDTRONIC NEUROMODULATION
- PMA / PMN Number
- P960009
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- PHYSICIAN
- Health Professional
- Yes
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Unknown | Required Intervention |