MiRus, LLC
FDA 510(k) medical device clearances.
Top product codes for MiRus, LLC
Recent clearances by MiRus, LLC
- K253444 — EUROPA Posterior Cervical Fusion Navigated Instruments
- K252733 — ATLAS Expandable Osteotomy Wedge System
- K242516 — EUROPA Posterior Cervical Fusion System
- K241175 — MiRus MoRe Lumbar Plating System
- K232348 — RIGEL 3DR Standalone Anterior Cervical Interbody Fusion System
- K232481 — RIGEL 3DR Anterior Cervical Corpectomy System
- K232154 — MiRus 3DR Lateral Lumbar Interbody Fusion System with Integrated Plate Fixation
- K230369 — EUROPA Navigated Instruments
- K220441 — CYGNUS MoRe Anterior Cervical Plate System
- K220115 — ANTARES 3DR Standalone Anterior Lumbar Interbody Fusion System
- K210800 — IO Expandable Lumbar Interbody Fusion System
- K200685 — RIGEL 3DR Anterior Cervical Interbody Fusion System
- K191906 — MiRus 3D Printed Lumbar Interbody Fusion Systems consisting of the Callisto 3D Printed PLIF, HYPERION 3D Printed TLIF, CALYPSO 3D Printed LLIF, and ANTARES 3D Printed ALIF
- K191867 — ATLAS Plating System
- K192268 — Europa Pedicle Screw System
- K191757 — EUROPA Pedicle Screw System
- K182524 — GALILEO Spine Alignment Monitoring System
- K190618 — RIGEL PEEK Anterior Cervical Interbody Fusion System
- K190666 — CYGNUS Anterior Cervical Plate System
- K190415 — ATLAS Plating System
- K180337 — EUROPA Pedicle Screw System
- K182920 — MiRus Lumbar Interbody Fusion System consisting of CALLISTO PEEK Posterior Lumbar Interbody Fusion (PLIF); HYPERION PEEK Transforaminal Lumbar Interbody Fusion (TLIF); CALPYSO PEEK Lateral Lumbar Interbody Fusion (LLIF); ANTARES PEEK Anterior Lumbar Interbody Fusion (ALIF)
- K182970 — EUROPA Pedicle Screw System
- K182989 — AURORA Screw System
Data sourced from openFDA. This site is unofficial and independent of the FDA.