meddevicedb.com FDA Device Reference

SABER-XA System

K261408 Class II Traditional
Decision Date
2026-08-03
Sponsor / Applicant
Elevation Spine

Technical Specification

510(k) Submission ID K261408
Product Code OVD
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2026-08-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SABER-XA System received FDA 510(k) clearance under submission number K261408, sponsored by Elevation Spine. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2026-08-03.

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.