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FOREX CORPORATION, OPTIMA, SPINAL SYSTEM

K020279 Class II Traditional
Decision Date
2002-06-20
Sponsor / Applicant
Forex Corp.

Technical Specification

510(k) Submission ID K020279
Product Code MNI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2002-06-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FOREX CORPORATION, OPTIMA, SPINAL SYSTEM received FDA 510(k) clearance under submission number K020279, sponsored by Forex Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2002-06-20.

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.