Mirus L L C

FDA Filings

This page includes the latest FDA filings for Mirus L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3014655115
FEI Number3014655115
NameMIRUS, LLC
Owner & OperatorMiRus, LLC
Contact Address1755 West Oak Parkway Suite 100
Marietta GA 30062 US
Official Correspondent
  • Rufus Prather Hamilton
  • 1-470-2070116-406
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1755 W Oak Parkway Suite 100
Marietta, GA 30062 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
MiRus, LLC
RIGEL 3DR Anterior Cervical Interbody Fusion System2020-06-11
MiRus, LLC
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 ALIF2020-05-18
MiRus, LLC
ATLAS Plating System2020-04-09
MiRus, LLC
Europa Pedicle Screw System2019-10-22
MiRus, LLC
EUROPA Pedicle Screw System2019-07-19
MiRus, LLC
GALILEO Spine Alignment Monitoring System2019-06-17
MiRus, LLC
RIGEL PEEK Anterior Cervical Interbody Fusion System2019-06-06
MiRus, LLC
CYGNUS™ Anterior Cervical Plate System2019-05-09
MiRus, LLC
ATLAS Plating System2019-04-19
MiRus, LLC
EUROPA Pedicle Screw System2019-03-14
MiRus, LLC
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 Lu2019-03-13
MiRus, LLC
EUROPA™ Pedicle Screw System2019-01-22
MiRus, LLC
AURORA™ Screw System2018-12-18

Related Finance Registrations
NCAGE Code7S2K9MIRUS LLC
NCAGE Code5HQ25MIRUS, LLC
CAGE Code5HQ25MIRUS, LLC

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