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TAURUS Posterior Occipital-Cervico-Thoracic Spinal Systems

K253195 Class II Traditional
Decision Date
2026-06-02
Sponsor / Applicant
ZheJiang Decans Medical Devices Co., Ltd.

Technical Specification

510(k) Submission ID K253195
Product Code NKG
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3075
Decision Date 2026-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TAURUS Posterior Occipital-Cervico-Thoracic Spinal Systems received FDA 510(k) clearance under submission number K253195, sponsored by ZheJiang Decans Medical Devices 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 2026-06-02.

Classification & Regulation

This clearance is catalogued under FDA product code NKG and 21 CFR 888.3075, within the Orthopedic review panel as a Class II device.