Zimvie (Zimmer Biomet Spine, Inc.) - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Zimvie (Zimmer Biomet Spine, Inc.) has 1 FDA 510(k) cleared medical devices. Based in Westminister, US.
Last cleared in 2022. Active since 2022. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Zimvie (Zimmer Biomet Spine, Inc.) Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Zimvie (Zimmer Biomet Spine, Inc.)
1 devices