BAAT Medical Products B.V.

BAAT Medical Products B.V. — FDA 510(k) Submissions

BAAT Medical Products B.V. has submitted 4 FDA 510(k) premarket notifications since 2020, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Rod, Fixation, Intramedullary And Accessories, Intervertebral Fusion Device With Bone Graft, Lumbar, Fastener, Fixation, Nondegradable, Soft Tissue, Growing Rod System . Use the specialty filter in the sidebar to narrow results.