From new and renewed partnerships to FDA approvals, here are 7 medtech stories we missed this week but thought were still worth mentioning. 1. Life Spine receives FDA clearance for cervical spacer system Life Spine announced in an April 19 press release that it has received FDA 510(k) clearance for its Plateau-C Ti Cervical Spacer […]
Mazor Robotics (NSDQ:MZOR) unveiled its next-generation robot-assisted surgery system and Globus Medical (NYSE:GMED) for the 1st time showcased the functional prototype of its Excelsius platform at the NASS 2016 meeting in Boston last week, signifying an increased interest in robotic surgeons among major players. Mazor developed 3 generations of products over 15 years and does 95% of its business in […]
Life Spine said today that it won 510(k) clearance from the FDA for its Pro-Link Ti cervical spacer. The Huntley, Ill.-based company said the product is slated for full release by the end of 2016, joining a portfolio of devices that Life Spine launched this year. The spacers allow for the fusion of adjacent segments […]
Centric Medical, the foot & ankle division of Life Spine, said yesterday that it won 510(k) clearance from the FDA for its subtalar arthroereisis implant for treating flatfoot deformities. The device is a 1-piece titanium implant designed to block forward, downward and medial displacement of the talus to allow normal articulation of the subtalar joint. The device is slated for limited release at […]
Life Spine said yesterday it won FDA 510(k) clearance for its Gruve anterior cervical plate system. The Gruve plate allows for extreme bone screw angulation, large graft windows and a locking mechanism that provides tactile and visual confirmation of locking upon installation, Huntley, Ill.-based Life Spine said. “Our comprehensive cervical portfolio reinforces Life Spine’s commitment to […]
October 21, 2014 by Brad Perriello
Life Spine launched a new division called Centric Medical, after receiving FDA marketing clearance for its Tarsa-Link system for internal bone fixation of fractures, fusions, and osteotomies in the foot and ankle.
The FDA gave Life Spine the green light for its Iris cervical plate, which incorporates a visual and tactile confirmation of the screw locking system. The 510(k) clearance for the Iris anterior cervical plate system is the 6th iteration of the company’s cervical platform.
"The IRIS ACP System adds to our comprehensive portfolio of intuitive cervical plating systems," said marketing director Rita Patel in prepared remarks.