Skip to content Skip to footer

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

PharmaShots! Your go-to media platform for customized news ranging for multiple indications. For more information connect with us at connect@pharmashots.com

Sign Up to Our Newsletter

Be the first to know the latest updates

[mc4wp_form id="13387" element_id="style-1"]