Retropsoas Technologies, LLC

Retropsoas Technologies, LLC — FDA 510(k) Submissions

Retropsoas Technologies, LLC has submitted 2 FDA 510(k) premarket notifications since 2024, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Intervertebral Fusion Device With Bone Graft, Lumbar, Stimulator, Nerve . Use the specialty filter in the sidebar to narrow results.