meddevicedb.com FDA Device Reference

E3D™-C Interbody System

K260038 Class II Special
Decision Date
2026-02-04
Sponsor / Applicant
Evolution Spine

Technical Specification

510(k) Submission ID K260038
Product Code OVE
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2026-02-04
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

E3D™-C Interbody System received FDA 510(k) clearance under submission number K260038, sponsored by Evolution Spine. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2026-02-04.

Classification & Regulation

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