FDA Adverse Event Injury Summary report: N

AEQUALIS RESURFACING HEAD

MDR report key: 6202019 · Received December 23, 2016

Report

Report Number
3000931034-2016-00230
Event Type
Injury
Date Received
December 23, 2016
Date of Event
November 23, 2016
Report Date
December 1, 2016
Manufacturer
TORNIER S.A.S.
Product Code
HSD
UDI-DI
03700386926945
PMA / PMN Number
K131231
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THIS IS THE FINAL REPORT SUBMITTED REGARDING THIS SURGICAL EVENT AND MEDICAL DEVICE.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT UNDERWENT A REVISION SURGERY DUE TO MALPOSITION. CONVERSION TO TSA.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
851782 AEQUALIS RESURFACING HEAD HUMERAL RESURFACING HSD TORNIER S.A.S. 43X16 03700386926945

Patients

Seq Age Sex Outcome Treatment
1 59 YR Other