meddevicedb.com FDA Device Reference

ENDIUS TITLE 2 POLYAXIAL SPINAL SYSTEM

K041808 Class II Special
Decision Date
2004-10-01
Sponsor / Applicant
Endius, Inc.

Technical Specification

510(k) Submission ID K041808
Product Code KWP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3050
Decision Date 2004-10-01
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDIUS TITLE 2 POLYAXIAL SPINAL SYSTEM received FDA 510(k) clearance under submission number K041808, sponsored by Endius, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2004-10-01.

Classification & Regulation

This clearance is catalogued under FDA product code KWP and 21 CFR 888.3050, within the Orthopedic review panel as a Class II device.