FDA Adverse Event Injury Summary report: N

AEQUALIS KEELED GLENOID UNKNOWN

MDR report key: 4687510 · Received April 8, 2015

Report

Report Number
9610667-2015-00024
Event Type
Injury
Date Received
April 8, 2015
Report Date
March 19, 2015
Manufacturer
TORNIER SAS
Product Code
KWS
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THIS IS THE FINAL REPORT SUBMITTED REGARDING THIS SURGICAL EVENT AND MEDICAL DEVICE. "WALCH G, MORAGA C, ET AL. (2012). RESULTS OF ANATOMIC NONCONSTRAINED PROSTHESIS IN PRIMARY OSTEOARTHRITIS WITH BICONCAVE GLENOID", J SHOULDER ELBOW SURG, 21:1526-1533.

Description of Event or Problem · 1

ONE PATIENT HAD REMOVAL OF GLENOID COMPONENT DUE TO GLENOID LOOSENING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
230458 AEQUALIS KEELED GLENOID UNKNOWN NONE KWS TORNIER SAS

Patients

Seq Age Sex Outcome Treatment
1 80 YR Required Intervention