Here are four spinal devices that have earned FDA approval, as reported by Becker’s since Jan. 24:
- The FDA cleared Spineart’s Perla TL application for use with eCential Robotics Op.nTM robotic navigation platform.
- Medical device company Life Spine earned FDA clearance for its Gruve+ cervical plating system.
- Life Spine earned FDA 510(k) clearance for its ProLift Pivot expandable spacer system.
- Saluda Medical earned FDA approval for its biomarker-based automated patient programming platform used in spinal cord stimulation.
At the Becker’s 32nd Annual Meeting: The Business and Operations of ASCs, taking place October 29-31 in Chicago, ASC leaders, surgeons and healthcare executives will explore strategies to drive growth, enhance operational performance, navigate reimbursement challenges and prepare for the future of ambulatory surgery. Apply for complimentary registration now.
