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MAGEC SPINAL BRACING AND DISTRACTION SYSTEM

K140613 Class II Traditional
Decision Date
2014-09-18
Sponsor / Applicant
Ellipse Technologies, Inc.

Technical Specification

510(k) Submission ID K140613
Product Code PGN
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2014-09-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MAGEC SPINAL BRACING AND DISTRACTION SYSTEM received FDA 510(k) clearance under submission number K140613, sponsored by Ellipse Technologies, 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 2014-09-18.

Classification & Regulation

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