DUBLIN--(BUSINESS WIRE)--The "Interbody Fusion Cage Market by Product Type, Surgery, and End User : Global Opportunity Analysis and Industry Forecast, 2021-2030" report has been added to ...
Please provide your email address to receive an email when new articles are posted on . Bioretec received FDA breakthrough device designation for its RemeOs spinal interbody cage. The cage is designed ...
From navigation systems to hardware, here are nine spine technologies earning FDA certifications and clearances since Jan. 19 ...
A collaboration between civil engineering and neurosurgery at the University of Pittsburgh could reshape spinal fusion surgery. Associate Professors Amir Alavi, Nitin Agarwal, and D. Kojo Hamilton ...
TAMPERE, Finland, Oct. 4, 2024 /PRNewswire/ -- Bioretec updates its product development strategy by accelerating the product development of the RemeOs ™ Spinal Interbody Cage, an innovative medical ...
ZURICH, SWITZERLAND / ACCESSWIRE / November 28, 2023 / Kuros Biosciences ("Kuros" or the "Company"), a leader in next generation bone graft technologies, announced today that MagnetOs Flex Matrix has ...
LYON, France & NEW YORK--(BUSINESS WIRE)--The Medicrea ® Group (Euronext Growth Paris: FR0004178572 - ALMED), pioneering the convergence of healthcare IT and next-generation, outcome-centered spinal ...
We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. The FDA has given 510(k) clearance to HAPPE Spine’s ...
TAMPERE, Finland, March 14, 2024 /PRNewswire/ -- Bioretec Ltd., a pioneer in biodegradable orthopedic implants, has today been granted Breakthrough Device Designation for its RemeOs™ Spinal Interbody ...
The use of implanted hardware in spinal fusion surgeries for lower back pain does not improve the results and carries a higher risk of complications, researchers reported today. The study published in ...
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