Medtronic (NYSE: MDT) announced today that it received FDA premarket approval (PMA) for the use of its Infuse bone graft in ...
Medtronic’s Infuse bone graft earned the FDA’s premarket approval for one- and two-level transforaminal lumbar interbody spinal fusions. The expanded approval allows use with PEEK and titanium ...
So far this year, medtech companies and academic institutions are making key strides in spine biologics. From new product launches to research breakthroughs, here are the biggest developments to know: ...
SC MEDICA announces a world first: the successful fully percutaneous, tubeless facet cage arthrodesis using the FFX® ...
Louisville is leading the charge in a handful of robotic-assisted surgeries, attracting patients from across the globe ...
(MENAFN- EIN Presswire) EINPresswire/ -- SC MEDICA today announced a world first: the successful fully percutaneous, tubeless facet cage arthrodesis. SC MEDICA's FFX ® Facet FiXation system was used ...
No significant association was seen between type of index operation and need for revision surgery among patients with degenerative lumbar spinal stenosis (DLSS), according to a cohort study. Among 328 ...
Life Spine, a medical device company that designs, develops, manufactures, and markets products for the surgical treatment of spinal disorders, announced today its ProLift(R) expandable interbody ...
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