meddevicedb.com FDA Device Reference

ISS INTEGRATED SPINE SYSTEM

K061524 Class II Traditional
Decision Date
2006-09-26
Sponsor / Applicant
Ortho Development Corp.

Technical Specification

510(k) Submission ID K061524
Product Code MNH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2006-09-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ISS INTEGRATED SPINE SYSTEM received FDA 510(k) clearance under submission number K061524, sponsored by Ortho Development Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2006-09-26.

Classification & Regulation

This clearance is catalogued under FDA product code MNH and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.