Nuvasive, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NuVasive AttraX Scaffold, NuVasive Modulus-C Interbody System, Simplify Disc
91
Total
90
Cleared
0
Denied
FDA 510(k) Regulatory Record - Nuvasive, Inc. General & Plastic Surgery ✕
4 devices