meddevicedb.com FDA Device Reference

TOSCA II ANTERIOR CERVICAL PLATE SYSTEM

K080815 Class II Special
Decision Date
2008-04-23
Sponsor / Applicant
Signus Medizintechnik GmbH

Technical Specification

510(k) Submission ID K080815
Product Code KWQ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 2008-04-23
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOSCA II ANTERIOR CERVICAL PLATE SYSTEM received FDA 510(k) clearance under submission number K080815, sponsored by Signus Medizintechnik GmbH. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2008-04-23.

Classification & Regulation

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