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 ...

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 ...

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 ...

Please provide your email address to receive an email when new articles are posted on . At this early stage in comparing extreme lateral lumbar interbody fusion and minimally invasive transforaminal ...

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 ...

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 ...

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 ...

(MENAFN- GlobeNewsWire - Nasdaq) Houston, TX, July 07, 2023 (GLOBE NEWSWIRE) -- Zion Market Research has published a new research report titled “Extreme Lateral Interbody Fusion (XLIF) Surgery Market ...

DBMR added a new research report on XLIF Surgery Market by Top players, Regions, Type and Application, Forecast to 2026 . XLIF Surgery market is studied By considering definite base year and historic ...

DUBLIN--(BUSINESS WIRE)--The "Global XLIF Surgery Market Analysis, Company Profiles, Size, Share, Growth, Trends and Forecast to 2024" report has been added to Research and Markets' offering. The ...