Medical Device Manufacturer · US , Westminister , CO

Zimvie Spine (Zimmer Biomet Spine, Inc.) - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2023

Total

Cleared

Denied

Zimvie Spine (Zimmer Biomet Spine, Inc.) has 4 FDA 510(k) cleared medical devices. Based in Westminister, US.

Latest FDA clearance: Apr 2024. Active since 2023. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Zimvie Spine (Zimmer Biomet Spine, Inc.) Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Zimvie Spine (Zimmer Biomet Spine, Inc.)

4 devices

1-4 of 4