Medical Device Manufacturer · US , Minneapolis , MN

Zimmer Spine - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2011

Total

Cleared

Denied

Zimmer Spine has 5 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 5 cleared submissions from 2011 to 2013. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Zimmer Spine

5 devices

1-5 of 5