Microport Navibot International, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Microport Navibot International, LLC has 1 FDA 510(k) cleared medical devices. Based in Foxborough, US.
Last cleared in 2022. Active since 2022. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Microport Navibot International, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Microport Navibot International, LLC
1 devices