Medical Device Manufacturer · US , Broomfield , CO

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

15 submissions · 15 cleared · Since 2017
15
Total
15
Cleared
0
Denied

Zimmer Biomet Spine, Inc. has 15 FDA 510(k) cleared orthopedic devices. Based in Broomfield, US.

Last cleared in 2021. Active since 2017.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by MRC Global, LLC as regulatory consultant.

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