meddevicedb.com FDA Device Reference

MEROPACK BIORESORBABLE NASAL PACKING AND SINUS STENT

K041381 Class I Traditional
Decision Date
2004-09-10
Sponsor / Applicant
Medtronic Xomed, Inc.

Technical Specification

510(k) Submission ID K041381
Product Code LYA
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4780
Decision Date 2004-09-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEROPACK BIORESORBABLE NASAL PACKING AND SINUS STENT received FDA 510(k) clearance under submission number K041381, sponsored by Medtronic Xomed, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2004-09-10.

Classification & Regulation

This clearance is catalogued under FDA product code LYA and 21 CFR 874.4780, within the Ear, Nose, Throat review panel as a Class I device.