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FDA 510(k) Applications Submitted by Kelly Stratton
FDA 510(k) Number
Submission Date
Device Name
Applicant
K190556
03/05/2019
Zimmer Biomet Universal Navigation System
Zimmer Biomet Spine, Inc.
K171907
06/26/2017
Vitality« Spinal Fixation System
Zimmer Biomet Spine, Inc.
K172275
07/28/2017
Vitality« Spinal Fixation System, Vitality«+ Power Instrument System
Zimmer Biomet Spine, Inc.
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