Nexus Spine, LLC
Nexus Spine, LLC holds FDA 510(k) medical device clearances, first cleared 2014, most recent 2025.
Top product codes for Nexus Spine, LLC
Recent clearances by Nexus Spine, LLC
- K243934 — Stable-L Lumbar Interbody System
- K241467 — Stable-C Interbody System
- K233375 — Tranquil-L Interbody System
- K240416 — Tranquil-C Interbody System
- K233234 — PressON Spinal Fixation System
- K231486 — Stable-L Standalone Lumbar Interbody System
- K232530 — Stable-L Standalone Lumbar Interbody System, Stable-C Interbody System
- K231763 — Stable-C Interbody System
- K223529 — PressON Spinal Fixation System
- K223627 — PreView-III Anterior Cervical Plate System
- K212498 — Stable-L Standalone Lumbar Interbody System
- K181621 — Stable-C Interbody System
- K181702 — Tranquil-L Interbody System
- K181483 — Tranquil Interbody System
- K170297 — Tranquil Interbody System
- K160820 — PressON Pro Spinal Fixation System
- K133287 — PRESSON SPINAL FIXATION SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.