FDA 510(k) Applications Submitted by NEXUS SPINE, LLC
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K133287 |
10/25/2013 |
PRESSON SPINAL FIXATION SYSTEM |
NEXUS SPINE, LLC |
K170297 |
01/31/2017 |
Tranquil Interbody System |
Nexus Spine, LLC |
K160820 |
03/24/2016 |
PressON Pro Spinal Fixation System |
Nexus Spine, LLC |
K181483 |
06/05/2018 |
Tranquil Interbody System |
Nexus Spine, LLC |
K231763 |
06/16/2023 |
Stable-C Interbody System |
Nexus Spine, LLC |
K181621 |
06/20/2018 |
Stable-C Interbody System |
Nexus Spine, LLC |
K181702 |
06/27/2018 |
Tranquil-L Interbody System |
Nexus Spine, LLC |
K212498 |
08/09/2021 |
Stable-L Standalone Lumbar Interbody System |
Nexus Spine, LLC |
K232530 |
08/21/2023 |
Stable-L Standalone Lumbar Interbody System, Stable-C Interbody System |
Nexus Spine, LLC |
K223529 |
11/23/2022 |
PressON Spinal Fixation System |
Nexus Spine, LLC |
K223627 |
12/05/2022 |
PreView-IIIÖ Anterior Cervical Plate System |
Nexus Spine, LLC |
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