FDA Adverse Event Injury Summary report: N

SPINAL IMPLANT

MDR report key: 21443 · Received April 24, 1995

Report

Report Number
MW1005720
Event Type
Injury
Date Received
April 24, 1995
Date of Event
September 8, 1992
Report Date
February 13, 1995
Manufacturer
UNKNOWN
Product Code
JDN
Adverse Event
Yes
Report Source
Voluntary report
Reporter Occupation
INVALID DATA

Narratives

Description of Event or Problem · 1

SINCE THE IMPLANT, RPTR HURTS ALL THE TIME NOW, MORE THAN BEFORE BACK SURGERY.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 32 YR Disability