FDA 510(k) Applications Submitted by Jared Crocker
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| 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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