meddevicedb.com FDA Device Reference

Stable-L Standalone Lumbar Interbody System, Stable-C Interbody System

K232530 Class II Special
Decision Date
2023-09-18
Sponsor / Applicant
Nexus Spine, LLC

Technical Specification

510(k) Submission ID K232530
Product Code OVD
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2023-09-18
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Stable-L Standalone Lumbar Interbody System, Stable-C Interbody System received FDA 510(k) clearance under submission number K232530, sponsored by Nexus Spine, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2023-09-18.

Classification & Regulation

This clearance is catalogued under FDA product code OVD and 21 CFR 888.3080, within the Orthopedic review panel as a Class II device.