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CAMBER SPINE COVERIS CERVICAL CAGE

K133529 Class II Traditional
Decision Date
2014-03-20
Sponsor / Applicant
Camber Spine

Technical Specification

510(k) Submission ID K133529
Product Code ODP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2014-03-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CAMBER SPINE COVERIS CERVICAL CAGE received FDA 510(k) clearance under submission number K133529, sponsored by Camber Spine. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2014-03-20.

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.