FDA 510(k) Applications Submitted by JULIE GANTENBERG

FDA 510(k) Number Submission Date Device Name Applicant
K153657 12/21/2015 Vanguard XP Knee System BIOMET, INC.
K141407 05/28/2014 VANGUARD XP FEMORAL COMPONENT(GEN II)/VANGUARD XP FEMORAL TRIAL BIOMET, INC.
K132873 09/13/2013 VANGUARD XP KNEE SYSTEM BIOMET, INC.
K143009 10/20/2014 Echo Bi-Metric Microplasty Hip System BIOMET, INC.


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