SI-Bone recieved additional FDA clearance for its iFuse Bedrock Granite device for sacroiliac joint fusions, the devicemaker said Dec. 27.
The new clearance adds indications for a variety of pedicle scerw systems, according to a news release. It will allow surgeons to use their preferred techniques and implants with iFuse Bedrock Granite.
Inital clearance included use with a single manufacturer’s pedicle screw system.
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…