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FDA 510(k) Applications Submitted by Amy Walriven
FDA 510(k) Number
Submission Date
Device Name
Applicant
K150503
02/26/2015
Echo Bi-Metric Microplasty Line Extension
BIOMET, INC.
K150522
03/02/2015
G7 Dual Mobility System
BIOMET, INC.
K140902
04/09/2014
E1 SERIES A PATELLAE, STANDARD 3-PEG, E1 SERIES A PATELLAE, THIN 3-PEG, E1 SERIES PATELLAE, ASYMMETRICAL, 3-PEG
BIOMET, INC.
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