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4S SPINAL SYSTEM

K063708 Class II Traditional
Decision Date
2007-04-24
Sponsor / Applicant
Taeyeon Medical Co., Ltd.

Technical Specification

510(k) Submission ID K063708
Product Code MNI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2007-04-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

4S SPINAL SYSTEM received FDA 510(k) clearance under submission number K063708, sponsored by Taeyeon Medical Co., 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 2007-04-24.

Classification & Regulation

This clearance is catalogued under FDA product code MNI and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.