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TigerPaw Pro Left Atrial Appendage Occlusion Fastener And Delivery Tool

K190884 Class II Traditional
Decision Date
2019-12-26
Sponsor / Applicant
Datascope Corp.

Technical Specification

510(k) Submission ID K190884
Product Code GDW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4750
Decision Date 2019-12-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TigerPaw Pro Left Atrial Appendage Occlusion Fastener And Delivery Tool received FDA 510(k) clearance under submission number K190884, sponsored by Datascope Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2019-12-26.

Classification & Regulation

This clearance is catalogued under FDA product code GDW and 21 CFR 878.4750, within the General, Plastic Surgery review panel as a Class II device.