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:
Jun. 12, 2018

Filed:

Feb. 15, 2013
Applicant:

Curaseal Inc., Santa Clara, CA (US);

Inventors:

Akshay Mavani, Los Alto, CA (US);

Kenton Fong, Mountain View, CA (US);

Leif Erik Bansner, Berkeley, CA (US);

Nathan Christopher Maier, Hayward, CA (US);

Dean Hu, San Leandro, CA (US);

Moshe Pinto, Mountain View, CA (US);

Harold Francis Carrison, Pleasanton, CA (US);

Eliot Kim, San Carlos, CA (US);

Assignee:

Curaseal Inc., Santa Clara, CA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61B 17/00 (2006.01);
U.S. Cl.
CPC ...
A61B 17/0057 (2013.01); A61B 2017/00004 (2013.01); A61B 2017/0061 (2013.01); A61B 2017/0065 (2013.01); A61B 2017/00579 (2013.01); A61B 2017/00588 (2013.01); A61B 2017/00592 (2013.01); A61B 2017/00597 (2013.01); A61B 2017/00601 (2013.01); A61B 2017/00606 (2013.01); A61B 2017/00623 (2013.01); A61B 2017/00641 (2013.01); A61B 2017/00898 (2013.01); A61B 2017/00902 (2013.01);
Abstract

Disclosed herein is a non-vascular fistula treatment system. The system may include a collapsible member, at least one tether, and a bioresorbable material. The collapsible member may be configured for positioning through a fistula tract and may comprise first and second disc members. The outer perimeter of the second disc member may be larger than the outer perimeter of the first disc member, and the first disc member may comprise a tether attachment structure. The at least one tether may be attached to the tether attachment structure. The bioresorbable material may be configured for placement in the fistula tract and may comprise a coupling structure configured to couple to the at least one tether. The second disc member may be configured to seal to a surface of a body lumen at a distal opening of the fistula tract and occlude the fistula tract at the distal opening.


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