meddevicedb.com FDA Device Reference

GORE-TEX(R) STRETCH VASCULAR GRAFT

K903931 Class II Traditional
Decision Date
1990-12-06
Sponsor / Applicant
W. L. Gore & Associates, Inc.

Technical Specification

510(k) Submission ID K903931
Product Code DSY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3450
Decision Date 1990-12-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GORE-TEX(R) STRETCH VASCULAR GRAFT received FDA 510(k) clearance under submission number K903931, sponsored by W. L. Gore & Associates, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1990-12-06.

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.