FDA 510(k) Applications Submitted by NICOLE J MEREDITH

FDA 510(k) Number Submission Date Device Name Applicant
K191625 06/18/2019 Persona Revision Knee System Zimmer Inc.
K181947 07/20/2018 Persona Revision Knee System Zimmer Inc.
K172524 08/21/2017 Zimmer Persona Personalized Knee System Zimmer, Inc.
K173417 11/01/2017 Zimmer Persona Personalized Knee System Zimmer, Inc.
K130143 01/22/2013 PERSONA NATURAL TIBIA BASEPLATES ZIMMER, INC.
K122765 09/10/2012 PERSONA NATURAL TIBIA BASEPLATES ZIMMER INC.
K161592 06/09/2016 Persona Partial Knee System BIOMET, INC.


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