meddevicedb.com FDA Device Reference

RIB LINK™ Fixation System

K252166 Class II Traditional
Decision Date
2026-02-26
Sponsor / Applicant
Globus Medical, Inc.

Technical Specification

510(k) Submission ID K252166
Product Code HRS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2026-02-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RIB LINK™ Fixation System received FDA 510(k) clearance under submission number K252166, sponsored by Globus Medical, 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 2026-02-26.

Classification & Regulation

This clearance is catalogued under FDA product code HRS and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.