FDA Adverse Event Injury Summary report: N

AVAULTA ANTERIOR BIOSYNTHETIC SUPPORT SYSTEM

MDR report key: 3152192 · Received May 16, 2013

Report

Report Number
1018233-2013-02034
Event Type
Injury
Date Received
May 16, 2013
Report Date
April 16, 2013
Manufacturer
SOFRADIM PRODUCTION
Product Code
FTL
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
GA, US
Reporter Occupation
ATTORNEY

Narratives

Description of Event or Problem · 1

(B)(4). THE PT'S ATTORNEY ALLEGED A DEFICIENCY AGAINST THE DEVICE. ADD'L INFO HAS BEEN REQUESTED, BUT NOT YET REC'D. ASSOCIATED MDR: 1018233-2013-01973 AND 02033.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
216476 AVAULTA ANTERIOR BIOSYNTHETIC SUPPORT SYSTEM FTL SOFRADIM PRODUCTION NA ZGG00514

Patients

Seq Age Sex Outcome Treatment
1 64 YR Required Intervention BOSTON SCIENTIFIC OBTRYX| AVAULT POSTERIOR BIOSYNTHETIC SUPPORT SYSTEM