The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Sep. 05, 2023

Filed:

Feb. 23, 2018
Applicant:

Boston Scientific Scimed, Inc., Maple Grove, MN (US);

Inventors:

Laszlo Trent Farago, Hudson, WI (US);

Mark A. Hilse, Ham Lake, MN (US);

Assignee:

Boston Scientific Scimed, Inc., Maple Grove, MN (US);

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
A61F 2/01 (2006.01); A61M 39/22 (2006.01); A61B 17/12 (2006.01); A61B 17/3207 (2006.01); A61B 17/221 (2006.01); A61M 25/10 (2013.01); A61B 17/22 (2006.01); A61B 90/00 (2016.01); A61B 17/00 (2006.01);
U.S. Cl.
CPC ...
A61F 2/013 (2013.01); A61B 17/1204 (2013.01); A61B 17/12109 (2013.01); A61B 17/22 (2013.01); A61M 25/104 (2013.01); A61M 39/22 (2013.01); A61B 2017/00893 (2013.01); A61B 2017/2215 (2013.01); A61B 2017/22079 (2013.01); A61B 2017/22084 (2013.01); A61B 2017/320716 (2013.01); A61B 2090/3966 (2016.02); A61B 2217/007 (2013.01); A61F 2230/0067 (2013.01);
Abstract

A medical device may include an elongate tubular member defining a tube lumen, and an expandable member disposed on the distal portion of the elongate tubular member including a lumen that is in fluid communication with the tube lumen. The expandable member is configured to expand from a collapsed delivery configuration to a distally-open expanded configuration and establish apposition with a vessel wall. A valve member in fluid communication with the tube lumen, and configured to selectively block and selectively allow for flow through the tube lumen. The device may be percutaneously-deployable downstream of a treatment site within a body lumen and may allow for selective removal and/or draining of fluid and/or material, such as embolic material, from a body lumen.


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