Fiagon GmbH earned FDA clearance for an extended platform for its spine navigation system, according to an Oct. 17 news release.
The company’s platform integrates electromagnetic navigation technology and is designed to decrese surgery time for minimally invasive spine cases.
Fiagon GmbH is based in Germany, and its portfolio also includes systems for pedicle screw placement, minimally invasive spinal fusion and endoscopic spine surgery.
Here are four spinal devices that have earned FDA approval, as reported by Becker’s since Jan. 24:
The FDA has cleared Spineart’s Perla TL application for use with eCential Robotics Op.nTM robotic navigation platform. The clearance will…
Here are six key updates from spine and orthopedic companies since March 5. 1. Aurora Spine completed enrollment for its…