FDA Adverse Event Injury Summary report: N

STAR TOTAL ANKLE REPLACEMENT

MDR report key: 3948930 · Received June 20, 2014

Report

Report Number
3003640913-2014-00051
Event Type
Injury
Date Received
June 20, 2014
Date of Event
May 19, 2014
Report Date
May 19, 2014
Manufacturer
SMALL BONE INNOVATIONS, INC.
Product Code
NTG
PMA / PMN Number
P050050
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
KS, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

VISUAL EXAMINATION CONFIRMS THE SLIDING CORE MOBILE BEARING WAS FRACTURED. THIS FRACTURE OCCURRED AFTER 15 YEARS OF IMPLANTATION.

Description of Event or Problem · 1

STAR TOTAL ANKLE REPLACEMENT SLIDING CORE MOBILE BEARING WAS EXCHANGED DUE TO IMPLANT FRACTURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
363102 STAR TOTAL ANKLE REPLACEMENT SLIDING CORE MOBILE BEARING NTG SMALL BONE INNOVATIONS, INC. 400-144

Patients

Seq Age Sex Outcome Treatment
1 73 YR Required Intervention