meddevicedb.com FDA Device Reference

MEDUSA VASCULAR PLUG,

K140796 Class II Traditional
Decision Date
2014-12-02
Sponsor / Applicant
Endoshape, Inc.

Technical Specification

510(k) Submission ID K140796
Product Code KRD
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3300
Decision Date 2014-12-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDUSA VASCULAR PLUG, received FDA 510(k) clearance under submission number K140796, sponsored by Endoshape, 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 2014-12-02.

Classification & Regulation

This clearance is catalogued under FDA product code KRD and 21 CFR 870.3300, within the Cardiovascular review panel as a Class II device.