From regulatory clearances to partnerships, here are five key developments from spine and orthopedic medtech companies since March 13
1. The FDA cleared Spineart’s Perla TL application for use with eCential Robotics Op.n robotic navigation platform. The clearance will combine Spineart and eCential Robotics’ robotic-assisted spine surgery technologies.
2. SynerFuse is partnering with Velentium Medical to scale the SynerFuse e-TLIF implant.
3. Tenon Medical earned FDA 510(k) clearance to use its Catamaran sacroiliac joint system for augmenting thoracolumbar fusion. With the new indication Catamaran can be used as a standalone treatment or to augment spinal fusion.
4. Aurora Spine earned FDA 510(k) clearance for its Aero facet fusion system. Aero is a minimally invasive system for facet joint-related pain or instability in levels C2 to S1. It can be used as a standalone or as an adjunct to larger spinal fusions.
5. Orthofix’s TrueLok Elevate transverse bone transplant system earned FDA 510(k) clearance and CE Mark from the European Union. TrueLok Elevate is designed for limb preservation and addresses bony or soft tissue deformities.
