FDA Adverse Event Injury Summary report: N

STAR TOTAL ANKLE REPLACEMENT

MDR report key: 3121767 · Received May 13, 2013

Report

Report Number
3003640913-2013-00020
Event Type
Injury
Date Received
May 13, 2013
Date of Event
April 12, 2013
Report Date
May 10, 2013
Manufacturer
SMALL BONE INNOVATIONS, INC.
Product Code
HSN
PMA / PMN Number
P050050
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

PATIENT HAD STAR SLIDING CORE BEARING COMPONENT REVISED AFTER 9 YEARS OF IMPLANTATION. VISUAL EVALUATION CONFIRMED POLY HAD NORMAL WEAR. DEVICE HISTORY RECORD SHOWED NO ANOMALIES.

Description of Event or Problem · 1

PATIENT HAD STAR SLIDING CORE BEARING COMPONENT REVISED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
211450 STAR TOTAL ANKLE REPLACEMENT STAR SLIDING CORE COMPONENT HSN SMALL BONE INNOVATIONS, INC. 400-142 0107150

Patients

Seq Age Sex Outcome Treatment
1 78 YR Required Intervention