FDA Clears for Augmented Reality Navigation Platform for Neurosurgery
The system is designed to give surgeons a clear, real-time view of critical anatomy and planned trajectories.Â
The system is designed to give surgeons a clear, real-time view of critical anatomy and planned trajectories.Â
The FDA approved marketing for CMR Surgical's Versius Surgical System, designed to assist in minimally invasive soft tissue surgeries.
ImmersiveTouch has received FDA clearance for its ImmersiveAR platform, an augmented reality technology to enhance surgical planning.
The system is designed to give surgeons a clear, real-time view of critical anatomy and planned trajectories.Â
Inovedis announced that the first patients were treated with the Sinefix Rotator Cuff Repair System as part of a pre-market clinical study.
Read MoreOlympus is recalling its Olympus High Flow Insufflation Unit because the unit may over-insufflate (inflate) air into the body with no warning.
Read MoreThe Joint Commission has issued Sentinel Event Alert for surgical teams on risk factors for surgical fires and how to prevent them.
Read MoreMedical device and technology company Lazurite has added Benchmark Medical as a distributor for its ArthroFree Wireless Camera System.
Read MoreLevita Magnetics has received FDA clearance for its Mars surgical platform which uses magnets for minimally invasive surgery.
Read MoreA peer-reviewed study showed the Hubly Drill with Smart Auto-Stop was effective and safe compared to established perforators.
Read More
The FDA has labeled the recall of two types of Megadyne electrodes manufactured by Johnson & Johnson’s Ethicon as a class I, the most serious.Â