Extreme lateral interbody fusion, in which one or two small incisions are made in the side of the body to access the disc space and perform fusion, was found to be less invasive and just as effective ...
NuVasive, a medical device company focused on developing minimally invasive spine surgery products, recently announced that both CIGNA and Humana changed their lumbar spinal fusion policy to include ...
WALTHAM, Mass., Dec. 16 According to Millennium Research Group (MRG), the global authority on medical technology market intelligence, although the US minimally invasive spinal fusion market will ...
NuVasive, Inc.NUVA recently received the FDA's 510 (k) clearance for its COHERE Porous PEEK implant to be used in eXtreme Lateral Interbody Fusion (XLIF) surgical spine procedures. The company plans ...
AUDUBON, Pa., Oct. 10, 2023 (GLOBE NEWSWIRE) -- Globus Medical, Inc. (NYSE: GMED), a leading musculoskeletal solutions company, celebrated twenty years of the NuVasive XLIF procedure at the Society ...
We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. Although minimally invasive extreme lateral interbody ...
In line with its expectation to launch COHERE XLIF in the United States by the second quarter of 2019, NuVasive, Inc. NUVA recently announced the first case using this technology. Cohere XLIF is the ...
UnitedHealthcare and Aetna have reversed their spinal procedure policies to cover Xtreme Lateral Interbody Fusion, or XLIF, according to news releases from NuVasive, a medical device company focused ...
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