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FDA 510(k) Applications Submitted by Anne-Marie Keefe
FDA 510(k) Number
Submission Date
Device Name
Applicant
K163034
10/31/2016
SUTUREFIX Curved Suture Anchor
Smith and Nephew, Inc.
K173901
12/22/2017
MyoSure MANUAL Tissue Removal Device
Hologic, Inc.
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