Johnson & Johnson MedTech’s DePuy Synthes this week announced it received FDA 510(k) clearance for its Teligen technology platform for spinal procedures.
Teligen is an integrated technology platform that enables minimally invasive surgical transforaminal lumber interbody fusion (MIS-TLIF) procedures using digital tools for visualization and access. The system has a tower with a camera control system, a VueLIF-T procedure kit with a disposable HD camera, a Teligen clear discectomy device and patient-based disposable ports.
DePuy Synthes’ new system integrates the company’s Unleash bundle of implant solutions that streamline the main stages in MIS-TLIF.
TLIF is a common posterior surgical approach used for treating patients with persistent pain in their lower backs and have spinal instability and fail to respond to noninvasive management. According to the company, TLIF can present clinical challenges like greater soft tissue disruptio…