NuVasive Receives First Ever FDA 510(k) Clearance of ... | 合法醫療器材資訊網

SAN DIEGO, CA — (Marketwired) — 10/12/15 — NuVasive, Inc.(NASDAQ: NUVA), a leading medical device company focused on transforming spine surgery with minimally disruptive, procedurally-integrated solutions, announced today the first ever FDA 510(k) clearance of a cervical corpectomy cage. The X-Core® Mini Cervical Corpectomy System is an expandable titanium vertebral body replacement device designed to provide enhanced stability following a corpectomy procedure. This first-of-its kind clearance further showcases NuVasive’s commitment to investing in innovative technology and clinical research to improve patient outcomes.

The NuVasive X-Core Mini Cervical Expandable VBR System (X-Core Mini VBR) is a vertebral body replacement device indicated for use in the cervical spine (C3-C7 vertebral bodies) in skeletally mature patients to replace a diseased or damaged ver...