FDA Adverse Event Injury Summary report: N

SPINAL IMPLANT

MDR report key: 19810 · Received February 16, 1995

Report

Report Number
MW1005155
Event Type
Injury
Date Received
February 16, 1995
Date of Event
October 1, 1986
Report Date
January 16, 1995
Manufacturer
UNKNOWN
Product Code
KWQ
Report Source
Voluntary report
Reporter Location
NC, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

CONSTANT PAIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SPINAL IMPLANT KWQ UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 66 YR Other| S