meddevicedb.com FDA Device Reference

SPICCA Cervical Fusion Cages

K230607 Class II Traditional
Decision Date
2023-08-14
Sponsor / Applicant
Southern Medical (Pty) , Ltd.

Technical Specification

510(k) Submission ID K230607
Product Code ODP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2023-08-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPICCA Cervical Fusion Cages received FDA 510(k) clearance under submission number K230607, sponsored by Southern Medical (Pty) , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2023-08-14.

Classification & Regulation

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