meddevicedb.com FDA Device Reference

Pounce Thrombectomy System

K220501 Class II Special
Decision Date
2022-03-23
Sponsor / Applicant
Surmodics,Inc.

Technical Specification

510(k) Submission ID K220501
Product Code QEW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5150
Decision Date 2022-03-23
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Pounce Thrombectomy System received FDA 510(k) clearance under submission number K220501, sponsored by Surmodics,Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2022-03-23.

Classification & Regulation

This clearance is catalogued under FDA product code QEW and 21 CFR 870.5150, within the Cardiovascular review panel as a Class II device.