NuVasive Receives FDA 510(k) Clearance to Market MAGEC System

NuVasive Specialized Orthopedics received FDA 510(k) clearance to market the MAGEC® system for implantation via the Reline® posterior fixation system to treat severe spinal deformity.

MAGEC received its first 510(k) clearance under Ellipse Technologies, in 1Q14. NuVasive acquired Ellipse earlier in 2016. Reline is integrated...

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Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.

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