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FDA 510(k) Applications Submitted by Anuja Yardi
FDA 510(k) Number
Submission Date
Device Name
Applicant
K162752
09/30/2016
ARTIA Reconstructive Tissue Matrix Perforated
LIFECELL CORPORATION
K213287
10/01/2021
StageOne Knee Cement Spacer Molds
Biomet, Inc.
K163647
12/23/2016
Revolve Envi 600 Advanced Adipose System
LifeCell Corporation
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