Aesculap Implant Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ArcadiusXP C Spinal System, AESCULAP PEEK XP SPINAL IMPLANT SYSTEM, S4 SPINAL SYSTEM
22
Total
22
Cleared
0
Denied
FDA 510(k) Regulatory Record - Aesculap Implant Systems, Inc. Neurology ✕
1 devices