TigerPaw Pro Left Atrial Appendage Occlusion Fastener And Delivery Tool

FDA 510(k) K190884 · Datascope Corp.

Substantially Equivalent

510(k) numberK190884

Submission

Device name
TigerPaw Pro Left Atrial Appendage Occlusion Fastener And Delivery Tool
Applicant
Datascope Corp.
Fairfield, NJ, US
Received
April 4, 2019
Decision date
December 26, 2019
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GDW – Staple, Implantable
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4750
Specialty
General, Plastic Surgery
Implant
Yes

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Questions and answers

When was TigerPaw Pro Left Atrial Appendage Occlusion Fastener And Delivery Tool cleared by the FDA?

TigerPaw Pro Left Atrial Appendage Occlusion Fastener And Delivery Tool (K190884) received a 510(k) decision of Substantially Equivalent on December 26, 2019, 266 days after the submission was received.

What is the product code of K190884?

The FDA product code is GDW – Staple, Implantable, a Class II (moderate risk) device regulated under 21 CFR 878.4750.