meddevicedb.com FDA Device Reference

LIFESPAN REINFORCED EPTFE STRAIGHT VASCULAR GRAFTS, EXTERNALLY SUPPORTED VASCULAR GRAFTS, STEPPED VASCULAR GRAFTS

K032900 Class II Traditional
Decision Date
2003-12-04
Sponsor / Applicant
Edwards Lifesciences, LLC

Technical Specification

510(k) Submission ID K032900
Product Code DSY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3450
Decision Date 2003-12-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIFESPAN REINFORCED EPTFE STRAIGHT VASCULAR GRAFTS, EXTERNALLY SUPPORTED VASCULAR GRAFTS, STEPPED VASCULAR GRAFTS received FDA 510(k) clearance under submission number K032900, sponsored by Edwards Lifesciences, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2003-12-04.

Classification & Regulation

This clearance is catalogued under FDA product code DSY and 21 CFR 870.3450, within the Cardiovascular review panel as a Class II device.