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December 15, 2023
The Food and Drug Administration cleared more than 200 spine-related devices and technologies with 510(k) approval in 2023.
November 27, 2023
FDA cleared 28 spine-related devices with 510(k) approval in October, including Vital Spinal Fixation System, Acro Composites Interbody System, Zeus Spinal Syst
November 21, 2023
The FDA granted 42 orthopedic-related 510(k) clearances in October, including Vital Spinal Fixation System, Tornier Humeral Nail, Acro Composites
March 30, 2023
Net Other expense - net 26 - Interest expense 1,009 1.2 ... | March 30, 2023
February 15, 2022
/PRNewswire/ -- SynerFuse, Inc., a privately held, clinical-stage medical device company focused on the development of a novel neuromodulation therapy concept...
February 15, 2022
/PRNewswire/ -- SynerFuse, Inc., a privately held, clinical-stage medical device company focused on the development of a novel neuromodulation therapy concept...
February 15, 2022
MINNEAPOLIS, Feb. 15, 2022 /PRNewswire/ -- SynerFuse, Inc., a privately held, clinical-stage medical device company focused on the development of ...