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FDA clears expanded use for NuVasive C360 portfolio

NuVasive announced today that it received FDA 510(k) clearance for use of its Modulus Cervical interbody implant with a bone void filler.

NuVasive Launches Tube System and Excavation Micro for Posterior Spine Surgery

/PRNewswire/ NuVasive, Inc. (NASDAQ: NUVA), the leader in spine technology innovation, focused on transforming spine surgery with minimally disruptive,.

NuVasive Launches Reline Cervical for Posterior Cervical Fusion as Part of the C360 Portfolio

/PRNewswire/ NuVasive, Inc. (NASDAQ: NUVA), the leader in spine technology innovation, focused on transforming spine surgery with minimally disruptive,.

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NuVasive receives FDA clearance for expanded indication of synthetic putty

NuVasive Inc. has announced FDA 510(k) clearance for expanded indication of Attrax putty for use in interbody fusion of the thoracolumbar spine, according to a press release.Attrax putty is a synthetic, biologic and osteoconductive bone void filler, which is designed to perform similar to autograft bone, according to the release.

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