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TSRH SPINAL SYSTEM

K052054 Class II Traditional
Decision Date
2005-08-16
Sponsor / Applicant
Medtronic Sofamor Danek

Technical Specification

510(k) Submission ID K052054
Product Code NKB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2005-08-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TSRH SPINAL SYSTEM received FDA 510(k) clearance under submission number K052054, sponsored by Medtronic Sofamor Danek. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2005-08-16.

Classification & Regulation

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