Aesculap Implant Systems, LLC - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
Aesculap Implant Systems, LLC has 22 FDA 510(k) cleared orthopedic devices. Based in Center Valley, US.
Last cleared in 2022. Active since 2010.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Aesculap Implant Systems, LLC
22 devices
Cleared
Jul 01, 2022
Ennovate Cervical Spinal and Occiput System
Orthopedic
200d
Cleared
Jul 19, 2021
ENNOVATE Spinal System
Orthopedic
110d
Cleared
Apr 26, 2018
ENNOVATE®
Orthopedic
65d
Cleared
Dec 14, 2016
ENNOVATE Spinal System
Orthopedic
135d
Cleared
Jul 08, 2016
Aesculap(R) Implant Systems (AIS) S4 Navigation Instruments
Orthopedic
198d
Cleared
May 16, 2016
Aesculap OrthoPilot Next Generation
Orthopedic
174d
Cleared
Oct 21, 2015
S4 Cervical Spinal and Occiput Systems
Orthopedic
99d
Cleared
Aug 13, 2015
Aesculap T-Space PEEK and XP Spinal System
Orthopedic
115d
Cleared
May 29, 2015
Columbus Total Knee System, Columbus Revision Knee System, EnduRo Knee System
Orthopedic
87d
Cleared
Feb 24, 2015
AESCULAP ORTHOPILOT NEXT GENERATION
Orthopedic
245d
Cleared
Feb 09, 2015
Excia Total Hip System
Orthopedic
27d
Cleared
Nov 21, 2014
VEGA Knee System
Orthopedic
23d