meddevicedb.com FDA Device Reference

MEDTRONIC MODEL 5407S, 5807S & 5410S SURG CABLES

K914460 Class II Traditional
Decision Date
1991-11-22
Sponsor / Applicant
Medtronic Vascular

Technical Specification

510(k) Submission ID K914460
Product Code DRF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1220
Decision Date 1991-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDTRONIC MODEL 5407S, 5807S & 5410S SURG CABLES received FDA 510(k) clearance under submission number K914460, sponsored by Medtronic Vascular. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1991-11-22.

Classification & Regulation

This clearance is catalogued under FDA product code DRF and 21 CFR 870.1220, within the Cardiovascular review panel as a Class II device.