meddevicedb.com FDA Device Reference

DEPUY PULSE CERVICAL CAGE SYSTEM

K120517 Class II Traditional
Decision Date
2012-04-26
Sponsor / Applicant
Medos International SARL

Technical Specification

510(k) Submission ID K120517
Product Code ODP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2012-04-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DEPUY PULSE CERVICAL CAGE SYSTEM received FDA 510(k) clearance under submission number K120517, sponsored by Medos International SARL. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2012-04-26.

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.