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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