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 ...
NuVasive (NUVA) commemorates industry-defining innovation in the lateral procedural segment SAN DIEGO, March 13, 2023 /PRNewswire/ -- NuVasive, Inc. (NASDAQ: NUVA), the leader in spine technology ...
NEW YORK_Shares of medical device maker NuVasive Inc. fell Tuesday, but rebounded off session lows, as investors remained concerned that health insurers will not reimburse doctors who use the ...
AUDUBON, Pa., Oct. 10, 2023 (GLOBE NEWSWIRE) -- Globus Medical, Inc. (GMED), a leading musculoskeletal solutions company, celebrated twenty years of the NuVasive XLIF procedure at the Society for ...
We were unable to process your request. Please try again later. If you continue to have this issue please contact [email protected]. Back to Healio The NuVasive Cohere Porous PEEK implant ...
We were unable to process your request. Please try again later. If you continue to have this issue please contact [email protected]. Back to Healio Although minimally invasive extreme ...
SAN DIEGO, Feb. 13, 2020 /PRNewswire/ --NuVasive, Inc. (NASDAQ: NUVA), the leader in spine technology innovation, focused on transforming spine surgery with minimally disruptive, procedurally ...
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