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EXTRA SOFT/EXTRA LOW WOVEN VASCULAR PROTHESIS

K910863 Class II Traditional
Decision Date
1991-04-01
Sponsor / Applicant
Vascutek, Ltd.

Technical Specification

510(k) Submission ID K910863
Product Code DSY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3450
Decision Date 1991-04-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXTRA SOFT/EXTRA LOW WOVEN VASCULAR PROTHESIS received FDA 510(k) clearance under submission number K910863, sponsored by Vascutek, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1991-04-01.

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.