meddevicedb.com FDA Device Reference

RABEA SPINAL IMPLANT

K043316 Class II Traditional
Decision Date
2005-02-07
Sponsor / Applicant
Signus Medizintechnik GmbH

Technical Specification

510(k) Submission ID K043316
Product Code MQP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 2005-02-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RABEA SPINAL IMPLANT received FDA 510(k) clearance under submission number K043316, sponsored by Signus Medizintechnik GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2005-02-07.

Classification & Regulation

This clearance is catalogued under FDA product code MQP and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.