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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K200685

RIGEL 3DR Anterior Cervical Interbody Fusion System · MiRus, LLC · decided 2020-06-11 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
RIGEL 3DR Anterior Cervical Interbody Fusion System14-5-30806MIRUS LLCODP00810051518986