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CERVICAL CAGE

K110915 Class II Abbreviated
Decision Date
2011-07-22
Sponsor / Applicant
Eisertech, LLC

Technical Specification

510(k) Submission ID K110915
Product Code ODP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2011-07-22
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CERVICAL CAGE received FDA 510(k) clearance under submission number K110915, sponsored by Eisertech, LLC. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2011-07-22.

Classification & Regulation

This clearance is catalogued under FDA product code ODP and 21 CFR 888.3080, within the Orthopedic review panel as a Class II device.