meddevicedb.com FDA Device Reference

Atlas Spine HiRISE™ Expandable Cervical Corpectomy System

K252560 Class II Traditional
Decision Date
2025-11-10
Sponsor / Applicant
Atlas Spine, Inc.

Technical Specification

510(k) Submission ID K252560
Product Code PLR
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 2025-11-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Atlas Spine HiRISE™ Expandable Cervical Corpectomy System received FDA 510(k) clearance under submission number K252560, sponsored by Atlas Spine, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2025-11-10.

Classification & Regulation

This clearance is catalogued under FDA product code PLR and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.