meddevicedb.com FDA Device Reference

Eleganz Fusion Screw System (Fusion Screw System)

K250251 Class II Traditional
Decision Date
2025-06-13
Sponsor / Applicant
Dev4

Technical Specification

510(k) Submission ID K250251
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2025-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Eleganz Fusion Screw System (Fusion Screw System) received FDA 510(k) clearance under submission number K250251, sponsored by Dev4. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2025-06-13.

Classification & Regulation

This clearance is catalogued under FDA product code HWC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.