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 medical devices. Based in Center Valley, US.

Last cleared in 2022. Active since 2010.

Browse the FDA 510(k) cleared devices submitted by Aesculap Implant Systems, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Aesculap Implant Systems, LLC

2 devices
1-2 of 2
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
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All22 Orthopedic 2