FDA 510(k) approval
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Regulatory
First Fully Immersive 3D Augmented Reality Surgical Navigation System Achieves FDA Approval For Precision Spine Surgery
SALT LAKE CITY, June 15, 2022 /PRNewswire/ — VisAR, an augmented reality surgical navigation system from healthcare technology leader Novarad™, receives FDA 510(k)…
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Biologics
Royal Biologics Announces FDA 510K Approval and U.S. Commercial Launch of the MAXX™-BMC Bone Marrow Aspirate Concentration System
June 1, 2022 – OrthoSpineNews – Royal Biologics (Hackensack, NJ) a company specializing on Advanced Cellular Technologies & Enhanced Autologous…
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Hospitals
EIT Emerging Implant Technologies Announces 510(k) Approval from the FDA for Full 3D Printed Cage Portfolio and Begins Commercialization in the U.S.
Emerging Implant Technologies GmbH (EIT), a German medical device manufacturer exclusively focused on creating innovative technologies for spinal application by…
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