Nu Vasive, Incorporated - FDA 510(k) Cleared Devices
Recent clearances: NuVasive CoRoent Small Interbody System, NuVasive Modulus ALIF System, Rod Registration Frame
112
Total
112
Cleared
0
Denied
FDA 510(k) Regulatory Record - Nu Vasive, Incorporated Ear, Nose, Throat ✕
1 devices