meddevicedb.com FDA Device Reference

MODIFICATON TO: PYRAMID +4 ANTERIOR LUMBAR PLATE SYSTEM

K080429 Class II Special
Decision Date
2008-04-30
Sponsor / Applicant
Medtronic Sofamor Danek USA, Inc.

Technical Specification

510(k) Submission ID K080429
Product Code KWQ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 2008-04-30
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATON TO: PYRAMID +4 ANTERIOR LUMBAR PLATE SYSTEM received FDA 510(k) clearance under submission number K080429, sponsored by Medtronic Sofamor Danek USA, 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 2008-04-30.

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.