Nexus Spine
Nexus Spine appears in FDA public data with 0 recalls, 19 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Jun 22, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 19
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K261279 | DeltaNEC Interbody System | Jun 22, 2026 |
| K253331 | PressON Spinal Fixation System | Oct 14, 2025 |
| K243934 | Stable-L Lumbar Interbody System | Apr 30, 2025 |
| K241467 | Stable-C Interbody System | Jul 17, 2024 |
| K233375 | Tranquil-L Interbody System | Mar 20, 2024 |
| K240416 | Tranquil-C Interbody System | Mar 12, 2024 |
| K233234 | PressON Spinal Fixation System | Oct 26, 2023 |
| K231486 | Stable-L Standalone Lumbar Interbody System | Oct 12, 2023 |
| K232530 | Stable-L Standalone Lumbar Interbody System, Stable-C Interbody System | Sep 18, 2023 |
| K231763 | Stable-C Interbody System | Aug 21, 2023 |
| K223529 | PressON Spinal Fixation System | May 2, 2023 |
| K223627 | PreView-III Anterior Cervical Plate System | Feb 2, 2023 |
| K212498 | Stable-L Standalone Lumbar Interbody System | Mar 18, 2022 |
| K181621 | Stable-C Interbody System | Oct 19, 2018 |
| K181702 | Tranquil-L Interbody System | Sep 21, 2018 |
| K181483 | Tranquil Interbody System | Aug 27, 2018 |
| K170297 | Tranquil Interbody System | Jun 27, 2017 |
| K160820 | PressON Pro Spinal Fixation System | Jun 28, 2016 |
| K133287 | PRESSON SPINAL FIXATION SYSTEM | Feb 25, 2014 |