FDA Adverse Event Injury Summary report: N

SPINAL IMPLANT

MDR report key: 26723 · Received July 21, 1995

Report

Report Number
MW4000732
Event Type
Injury
Date Received
July 21, 1995
Date of Event
July 8, 1991
Report Date
March 1, 1995
Manufacturer
UNKNOWN
Product Code
JDN
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
OK, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

HAD BACK SURGERY 11/91. NO PHYSICAL TRAINING OF ANY KIND. HAD BACK SURGERY IN 12/92. HAD IMPLANT PLACED ON BACK. HAD PHYSICIAL THERAPY OTHER SURGERY. STILL HAVE PROBLEMS WITH BACK, LOSS CONTROL OF RIGHT LEG AND PAIN.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 39 YR Disability