FDA Adverse Event Injury Summary report: N

ORTHO

MDR report key: 751636 · Received July 9, 2003

Report

Report Number
MW1036430
Event Type
Injury
Date Received
July 9, 2003
Report Date
July 9, 2003
Manufacturer
ORTHO
Product Code
NBN
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
CA, US
Reporter Occupation
PATIENT

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ORTHO EXTRACORPOREAL SHOCK WAVE THERAPY NBN ORTHO * *

Patients

Seq Age Sex Outcome Treatment
1 62 YR Life Threatening| O| S