The US FDA Grants 510(k) Clearance to Medivis’ Spine Navigation Platform
Shots:
- The US FDA has granted 510(k) clearance to Spine Navigation platform; commercially launched in the US, making it available nationwide to hospitals & ambulatory surgical centers
- Spine Navigation integrates AI-driven surgical intelligence, real-time insights, & advanced imaging with lightweight AR hardware allowing surgeons ergonomic freedom using hand tracking & voice control in neuro & orthopedic surgeries
- Spine Navigation allows holographic navigation for spine procedures, seamlessly integrating with major imaging & hardware systems through its minimal-footprint workstation & intuitive instrumentation for easy operating rooms deployment
Ref: Prnewswire | Image: Medivis
Related News:- The US FDA Grants 510(k) Clearance to Teleflex’s AC3 Range Intra-Aortic Balloon Pump (IABP) for Cardiac Patient Mobility
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Ridhi is an avid secondary researcher who follows trends in the biopharmaceutical and healthcare sectors to curate engaging content for the global audience. She works as a news editor at PharmaShots and loves to read books and explore new destinations.
