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