Medical Device Manufacturer · US , Mequon , WI

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

5 submissions · 5 cleared · Since 2019

Total

Cleared

Denied

Titan Spine, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mequon, US.

Historical record: 5 cleared submissions from 2019 to 2020. Primary specialty: Orthopedic.

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

FDA 510(k) cleared devices by Titan Spine, Inc.

5 devices

1-5 of 5