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SPINAL ELEMENTS CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM

K122771 Class II Traditional
Decision Date
2013-01-10
Sponsor / Applicant
Spinal Elements, Inc.

Technical Specification

510(k) Submission ID K122771
Product Code OVE
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2013-01-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPINAL ELEMENTS CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM received FDA 510(k) clearance under submission number K122771, sponsored by Spinal Elements, 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 2013-01-10.

Classification & Regulation

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