Medicrea International S.A.S. (Medtronic)

Medicrea International S.A.S. (Medtronic) — FDA 510(k) Submissions

Medicrea International S.A.S. (Medtronic) has submitted 3 FDA 510(k) premarket notifications since 2024, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Intervertebral Fusion Device With Bone Graft, Lumbar, Automated Radiological Image Processing Software . Use the specialty filter in the sidebar to narrow results.