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NuVasive Gains FDA Clearance for Monolith Corpectomy -

NuVasive received FDA 510(k) clearance to market an expanded indication for use of its Monolith® modular PEEK corpectomy system in the cervical spine to treat damage caused by fracture, tumors and osteomyelitis or to support reconstruction following corpectomy performed to achieve decompression of the spinal cord and neural tissue in cervical degenerative disorders. (NuVasive, Inc., 12/10/18)