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PHANTOM PLUS CERAMIC CAGE SYSTEM

K121892 Class II Special
Decision Date
2012-08-24
Sponsor / Applicant
Amedica Corp.

Technical Specification

510(k) Submission ID K121892
Product Code MAX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2012-08-24
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHANTOM PLUS CERAMIC CAGE SYSTEM received FDA 510(k) clearance under submission number K121892, sponsored by Amedica Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2012-08-24.

Classification & Regulation

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