MSFX MIKRON PEEK CAGES
Dec 2025
108d
Mikron Makina Sanayi VE Tic. Ltd. Sti. has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Intervertebral Fusion Device With Bone Graft, Cervical . Use the specialty filter in the sidebar to narrow results.