Press Releases

MiRus® Receives FDA Clearance for Lowest Profile Anterior Cervical Plate System.

MiRus is pleased to announce recent FDA 510(k) clearance of the CYGNUS™ Anterior Cervical Plate System, the narrowest and thinnest cervical plate on the market.
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First System for Dynamic Intra-operative Measurement of Segmental and Global Spine Alignment Receives FDA Clearance.

MiRus is pleased to announce FDA 510(k) clearance of the GALILEO™ Spine Alignment Monitoring System, a non-optical, wireless, real-time measurement system for segmental and global sagittal spine alignment.
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MiRus Aquires 50,000 SQFT Manufacturing Facility.

Following the 510(k) clearance by FDA in March 2019 of MoRe®, a proprietary molybdenum rhenium superalloy for medical implants, MiRus is excited to announce a major expansion of its manufacturing capacity with the addition of a fully operational 50,000 sqft orthopaedic and spine manufacturing plant in Marietta, GA.
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MiRus Receives FDA 510(k) Approval for First Medical Implant with New Superalloy.

MiRus has received FDA 510(k) approval for the MoRe® based Europa™ Pedicle Screw System making it the first FDA approved medical device with this new class of implant material.
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MiRus™ Wins Two 2018 Spine Technology Awards

For Immediate Release Atlanta – September 17, 2018– MiRus™ Wins Two 2018 Spine Technology Awards Winning Multiple Awards in One Year, MiRus Takes Honors for EUROPA™ Pedicle Screw System and GALILEO™ Spine Alignment Monitoring System MiRus has won the Annual Spine Technology Awards for both of its initial products in the implant and navigation categories. The Spine Technology Awards are …

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