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FDA 510(k) Applications Submitted by Zimmer Biomet Spine Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K203218
11/02/2020
CaP Spheres Pellet Pack
Zimmer Biomet Spine Inc.
K171495
05/22/2017
Zyston Strut Open Titanium Spacer System
Zimmer Biomet Spine Inc.
K163543
12/16/2016
Biomet Fusion System
Zimmer Biomet Spine Inc.
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