NuVasive Extends First-Of-Its-Kind Porous PEEK Interbody To TLIF And PLIF Procedures

Company also receives expanded FDA 510(k) clearance for COALESCE™ Thoracolumbar Interbody Fusion Device and COHERE® Cervical Interbody Fusion Device for multi-level cases from C2-T1

SAN DIEGO, Jan. 4, 2018 -- (Healthcare Sales & Marketing Network) ... Devices, Orthopaedic, Neurosurgery, FDA, Product Launch NuVasive, COALESCE, Interbody Fusion Device

Source: HSMN NewsFeed - January 4, 2018 Category: Pharmaceuticals Source Type: news