Dr. Daniel Sciubba the first to use the Teligen system at Northwell Health in a Dec. 3 surgery to remove a spinal tumor from ...
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GlobalData on MSNZimmer Biomet’s total shoulder replacement system gains FDA 510(k) clearanceZimmer Biomet has gained 510(k) clearance from the US Food and Drug Administration (FDA) for the OsseoFit Stemless Shoulder ...
Former House Speaker Nancy Pelosi had hip replacement surgery Saturday at a U.S. military hospital in Germany after falling ...
Over 90% of hernia repairs are currently performed in the ASC setting, and the new robot is specifically tailored for those environments. The robot's design and form factor are both small, making it ...
Additional details can be found on the Form ... FDA clearance before it can market its products. Monogram cannot estimate the ...
Inc., an innovator in the field of orthopedic surgical robots, today announced that its TMINI ® Miniature Robotic System has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) ...
said Stuart Simpson, president, and chief executive officer of THINK Surgical. "We are very enthusiastic about receiving this clearance for use with the THINK Surgical TMINI System platform ...
Augmedics, a pioneer in augmented reality (AR) surgical navigation, today announced FDA 510(k) clearance of a new registration method for its xvision Spine System®. The xvision CT-to-fluoroscopy ...
surgical navigation, today announced FDA 510(k) clearance of a new registration method for its xvision Spine System®. The xvision CT-to-fluoroscopy (CT-Fluoro) registration method allows surgeons to ...
CHICAGO--(BUSINESS WIRE)--Augmedics, a pioneer in augmented reality (AR) surgical navigation, today announced FDA 510(k) clearance of a new registration method for its xvision Spine System®.
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