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CD SPINAL SYSTEM

K964159 Class II Traditional
Decision Date
1997-10-16
Sponsor / Applicant
Sofamor Danek USA,Inc.

Technical Specification

510(k) Submission ID K964159
Product Code KWP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3050
Decision Date 1997-10-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CD SPINAL SYSTEM received FDA 510(k) clearance under submission number K964159, sponsored by Sofamor Danek USA,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 1997-10-16.

Classification & Regulation

This clearance is catalogued under FDA product code KWP and 21 CFR 888.3050, within the Orthopedic review panel as a Class II device.