meddevicedb.com FDA Device Reference

Cervical Spine Truss System (CSTS)

K231739 Class II Traditional
Decision Date
2023-09-25
Sponsor / Applicant
4Web Medical, Inc.

Technical Specification

510(k) Submission ID K231739
Product Code OVE
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2023-09-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Cervical Spine Truss System (CSTS) received FDA 510(k) clearance under submission number K231739, sponsored by 4Web 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 2023-09-25.

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.