FDA Adverse Event Injury Summary report: N

AVAULTA BIOSYNTHETIC SUPPORT SYSTEM

MDR report key: 2822823 · Received August 5, 2009

Report

Report Number
1018233-2009-00092
Event Type
Injury
Date Received
August 5, 2009
Report Date
August 5, 2009
Manufacturer
SOFRADIM PRODUCTION
Product Code
FTL
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
WV, US
Reporter Occupation
ATTORNEY

Narratives

Description of Event or Problem · 1

IT WAS ALLEGED BY THE PT'S ATTORNEY FOLLOWING AN ANTERIOR REPAIR AND A POSTERIOR REPAIR PERFORMED IN 2007, "THE PT EXPERIENCED MENTAL AND PHYSICAL PAIN AND SUFFERING, PERMANENT INJURY, PHYSICAL DEFORMITY, LOSS OF A BODILY ORGAN SYSTEM AND HAS UNDERGONE OR WILL UNDERGO CORRECTIVE SURGERY OR SURGERIES". THE PT'S ATTORNEY PROVIDED THE PT'S IMPLANT CARD. THE DIAGNOSIS AND TYPE OF TREATMENT FOR THIS SPECIFIC PT IS NOT KNOWN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 AVAULTA BIOSYNTHETIC SUPPORT SYSTEM FTL FTL SOFRADIM PRODUCTION NA ZGK00107

Patients

Seq Age Sex Outcome Treatment
1 53 YR Required Intervention