Medical Device Manufacturer · US , Center Valley , PA

Aesculap Implant Systems, LLC - FDA 510(k) Cleared Devices

22 submissions · 22 cleared · Since 2010
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) Regulatory Record - Aesculap Implant Systems, LLC
22 devices
1-12 of 22
Cleared Jul 01, 2022
Ennovate Cervical Spinal and Occiput System
K213871 · NKG
Orthopedic · 200d
Cleared Jul 19, 2021
ENNOVATE Spinal System
K210963 · NKB
Orthopedic · 110d
Cleared Apr 26, 2018
ENNOVATE®
K180433 · NKB
Orthopedic · 65d
Cleared Dec 14, 2016
ENNOVATE Spinal System
K162134 · NKB
Orthopedic · 135d
Cleared Jul 08, 2016
Aesculap(R) Implant Systems (AIS) S4 Navigation Instruments
K153700 · OLO
Orthopedic · 198d
Cleared May 16, 2016
Aesculap OrthoPilot Next Generation
K153396 · OLO
Orthopedic · 174d
Cleared Oct 21, 2015
S4 Cervical Spinal and Occiput Systems
K151938 · NKG
Orthopedic · 99d
Cleared Aug 13, 2015
Aesculap T-Space PEEK and XP Spinal System
K151056 · MAX
Orthopedic · 115d
Cleared May 29, 2015
Columbus Total Knee System, Columbus Revision Knee System, EnduRo Knee System
K150544 · JWH
Orthopedic · 87d
Cleared Feb 24, 2015
AESCULAP ORTHOPILOT NEXT GENERATION
K141694 · OLO
Orthopedic · 245d
Cleared Feb 09, 2015
Excia Total Hip System
K150062 · LZO
Orthopedic · 27d
Cleared Nov 21, 2014
VEGA Knee System
K143106 · JWH
Orthopedic · 23d
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