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OCTAFIX OCCIPITAL CERVICAL PLATING SYSTEM

K021009 Class II Traditional
Decision Date
2002-06-18
Sponsor / Applicant
Spinal Concepts, Inc.

Technical Specification

510(k) Submission ID K021009
Product Code KWP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3050
Decision Date 2002-06-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OCTAFIX OCCIPITAL CERVICAL PLATING SYSTEM received FDA 510(k) clearance under submission number K021009, sponsored by Spinal Concepts, 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 2002-06-18.

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.