Please provide your email address to receive an email when new articles are posted on . MiRus received FDA breakthrough device designation for its Europa posterior cervical system. The system features ...

The MarketWatch News Department was not involved in the creation of this content. ATLANTA, Feb. 23, 2026 /PRNewswire/ -- MiRus(R) today announced FDA 510(k) clearance and commercial launch of the ...

ATLANTA, Aug. 1, 2025 /PRNewswire/ -- MiRus has received New Technology Add-on Payment (NTAP) from the Centers for Medicare and Medicaid Services (CMS) for the EUROPA® Posterior Cervical System, based ...

ATLANTA, June 11, 2020 /PRNewswire/ -- MiRus is pleased to announce that it received FDA 510(k) clearance for its 3DR™ (Randomized) Printed Lumbar Interbody Fusion System which consists of the ...

ATLANTA, July 26, 2019 /PRNewswire/ -- 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.

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. MiRus announced it has received FDA 510(k) approval for ...

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. The unique I-beam design and metal ...

ATLANTA, Sept. 18, 2023 /PRNewswire/ -- MiRus announces limited market release in the U.S. of its ATLAS™ MoRe ® Foot and Ankle Plating System, the thinnest foot and ankle plate on the market for ...

ATLANTA, Feb. 23, 2026 /PRNewswire/ -- MiRus® today announced FDA 510(k) clearance and commercial launch of the IO™ Expandable Wedge Osteotomy System, an innovative solution designed to bring ...

ATLANTA, Dec. 3, 2025 /PRNewswire/ -- MiRus is excited to announce that patients who benefit from health coverage through Centers for Medicare and Medicaid Services (CMS) have been the beneficiary ...