Aesculap Implant System, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AIS Odontoid Fracture Fixation System, AIS MODULIFT VBR SYSTEM, AIS MODULIFT VBR SYSTEM
18
Total
18
Cleared
0
Denied
FDA 510(k) Regulatory Record - Aesculap Implant System, Inc. Neurology ✕
1 devices