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ELLIPSE OCCIPITO-CERICO-THORACIC SPINAL SYSTEM

K090565 Class II Special
Decision Date
2009-06-30
Sponsor / Applicant
Globus Medical, Inc.

Technical Specification

510(k) Submission ID K090565
Product Code KWP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3050
Decision Date 2009-06-30
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELLIPSE OCCIPITO-CERICO-THORACIC SPINAL SYSTEM received FDA 510(k) clearance under submission number K090565, sponsored by Globus Medical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2009-06-30.

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.