FDA Adverse Event
Injury
Summary report: N
PAIN CARE 3000
MDR report key: 2142360
·
Received June 20, 2011
Report
- Report Number
- 2028253-2011-00029
- Event Type
- Injury
- Date Received
- June 20, 2011
- Date of Event
- June 14, 2005
- Report Date
- June 17, 2011
- Manufacturer
- BREG, INC
- Product Code
- FRN
- PMA / PMN Number
- K002073
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MN, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
PT HAD L SHOULDER ARTHROSCOPIC BANKHART REPAIR. DIAGNOSIS OF CHONDROLYSIS ON (B)(6)2009.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PAIN CARE 3000 | 88 FRN | FRN | BREG, INC | 10314 | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other| S |