Eit Emerging Implant Technologies GmbH - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Eit Emerging Implant Technologies GmbH has 5 FDA 510(k) cleared medical devices. Based in Wurmlingen, DE.
Historical record: 5 cleared submissions from 2017 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Eit Emerging Implant Technologies GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Eit Emerging Implant Technologies GmbH
5 devices
Cleared
Jul 15, 2020
EIT Cellular Titanium Cervical Cage, EIT Cellular Titanium ALIF Cage, EIT...
Orthopedic
30d
Cleared
Feb 04, 2019
EIT Cellular Titanium Lumbar Cage - T/PLIF
Orthopedic
54d
Cleared
Oct 12, 2018
EIT Cellular Titanium® Lumbar Cage LLIF
Orthopedic
112d
Cleared
Dec 15, 2017
EIT Cellular Titanium® Cervical Cages, EIT Cellular Titanium® PLIF Cages, EIT...
Orthopedic
85d
Cleared
Jul 11, 2017
EIT Cellular Titanium Cervical Cage, EIT Cellular Titanium PLIF Cages, EIT...
Orthopedic
140d