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ARENA-C CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM

K113518 Class II Abbreviated
Decision Date
2012-02-16
Sponsor / Applicant
Spinefrontier, Inc.

Technical Specification

510(k) Submission ID K113518
Product Code ODP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2012-02-16
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ARENA-C CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM received FDA 510(k) clearance under submission number K113518, sponsored by Spinefrontier, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2012-02-16.

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.