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FDA 510(k) Applications Submitted by Nicole 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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