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.
510(k) submissions have been managed by Shanghai MicroPort Medical (Group) Co., Ltd. as regulatory consultant.
1 devices