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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact