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FDA 510(k) Applications Submitted by Megan Fessenden
FDA 510(k) Number
Submission Date
Device Name
Applicant
K171495
05/22/2017
Zyston Strut Open Titanium Spacer System
Zimmer Biomet Spine Inc.
K132435
08/05/2013
SMITH & NEPHEW GLOBAL FEMORAL HEAD TRIALS
SMITH & NEPHEW, INC.
K142865
09/30/2014
Nellcor Bedside SpO2 Patient Monitoring System
Covidien LLC
K163543
12/16/2016
Biomet Fusion System
Zimmer Biomet Spine Inc.
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