meddevicedb.com FDA Device Reference

EXCELLA-M SPINAL SYSTEM

K042143 Class II Traditional
Decision Date
2004-10-07
Sponsor / Applicant
Innovasis, Inc.

Technical Specification

510(k) Submission ID K042143
Product Code KWP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3050
Decision Date 2004-10-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXCELLA-M SPINAL SYSTEM received FDA 510(k) clearance under submission number K042143, sponsored by Innovasis, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2004-10-07.

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.