Retropsoas Technologies, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Retropsoas Technologies, LLC has 2 FDA 510(k) cleared medical devices. Based in Frontenac, US.
Latest FDA clearance: Oct 2024. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Retropsoas Technologies, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Spitrex 3D (Watershed Idea Foundry, Inc. Dba Spitrex 3D) as regulatory consultant.
2 devices