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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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