US 12,472,069 B2
Methods for sacroiliac joint stabilization
Richard S Ginn, Gilroy, CA (US)
Assigned to Tenon Medical, Inc., Los Gatos, CA (US)
Filed by Tenon Medical, Inc., Los Gatos, CA (US)
Filed on May 10, 2022, as Appl. No. 17/740,568.
Application 17/740,568 is a continuation in part of application No. 17/463,779, filed on Sep. 1, 2021, granted, now 12,427,027.
Application 17/463,779 is a continuation in part of application No. 13/857,977, filed on Apr. 5, 2013, granted, now 11,273,042, issued on Mar. 15, 2022.
Application 13/857,977 is a continuation of application No. 13/192,289, filed on Jul. 27, 2011, abandoned.
Claims priority of provisional application 61/368,233, filed on Jul. 27, 2010.
Prior Publication US 2022/0273447 A1, Sep. 1, 2022
Int. Cl. A61F 2/30 (2006.01); A61B 5/055 (2006.01); A61B 5/06 (2006.01); A61B 6/00 (2006.01); A61B 6/03 (2006.01); A61B 8/08 (2006.01); A61B 17/16 (2006.01); A61B 17/70 (2006.01); A61B 17/88 (2006.01); A61B 34/20 (2016.01); A61F 2/44 (2006.01); A61F 2/46 (2006.01)
CPC A61F 2/30988 (2013.01) [A61B 5/055 (2013.01); A61B 5/062 (2013.01); A61B 6/032 (2013.01); A61B 6/485 (2013.01); A61B 8/0841 (2013.01); A61B 17/1604 (2013.01); A61B 17/1664 (2013.01); A61B 17/1671 (2013.01); A61B 17/70 (2013.01); A61B 17/7055 (2013.01); A61B 17/7074 (2013.01); A61B 17/8858 (2013.01); A61B 34/20 (2016.02); A61F 2/4455 (2013.01); A61F 2/4601 (2013.01); A61F 2/4611 (2013.01); A61B 2576/00 (2013.01); A61F 2002/30121 (2013.01); A61F 2002/30123 (2013.01); A61F 2002/30166 (2013.01); A61F 2002/30593 (2013.01); A61F 2002/30995 (2013.01)] 34 Claims
OG exemplary drawing
 
1. A method for stabilizing a dysfunctional sacroiliac (SI) joint of a subject, said subject comprising an anatomical structure, said dysfunctional SI joint comprising a dorsal recess, said method comprising the steps of:
a. providing a tool assembly adapted to access said dysfunctional SI joint via a posterior approach, said dysfunctional SI joint being disposed between and defined by a sacrum bone structure and an ilium bone structure,
said tool assembly comprising a guide pin configured and adapted to be positioned in said dysfunctional SI joint and a drill guide assembly,
said drill guide assembly adapted to create a pilot SI joint opening in said dysfunctional SI joint, said drill guide assembly comprising a guide member lumen that extends through said drill guide assembly, said guide member lumen adapted to receive said guide pin therein,
said drill guide assembly further comprising a bone dislodging member comprising a longitudinal axis, said bone dislodging member adapted to dislodge portions of bone in said dysfunctional SI joint,
said pilot SI joint opening comprising a first portion disposed in said sacrum bone structure and comprising a first sacrum opening cross-sectional shape and a second portion disposed in said ilium bone structure and comprising a first ilium opening cross-sectional shape,
said pilot SI joint opening further comprising a cross-sectional shape in a plane that intersects said sacrum bone structure and said ilium bone structure, said plane being substantially perpendicular to said longitudinal axis of said bone dislodging member when said bone dislodging member is disposed in a pilot SI joint opening creation position in said dysfunctional SI joint;
b. providing a prosthesis deployment assembly, said prosthesis deployment assembly comprising an elongated guide member and a prosthesis engagement rod, said prosthesis engagement rod comprising a threaded distal end,
said elongated guide member comprising a guide member proximal end and a guide member distal end disposed opposite said guide member proximal end,
said elongated guide member further comprising a prosthesis guide pin that extends from said guide member distal end, said elongated guide member further comprising a prosthesis engagement rod lumen adapted to receive said prosthesis engagement rod therein;
c. providing a SI joint prosthesis configured and adapted to be inserted into said pilot SI joint opening created by said drill guide assembly, said SI joint prosthesis comprising first and second elongated partially cylindrical sections connected to a bridge section, whereby said SI joint prosthesis comprises a continuous exterior surface comprising first and second partially cylindrical surface regions, said first partially cylindrical surface region comprising a first partially cylindrical surface region shape that corresponds to at least a first portion of said first sacrum opening cross-sectional shape, said second partially cylindrical surface region comprising a second partially cylindrical surface region shape that corresponds to at least a first portion of said first ilium opening cross-sectional shape,
said bridge section comprising a bridge section proximal end and a bridge section distal end disposed opposite said bridge section proximal end,
said bridge section distal end comprising a first tapered region configured and adapted to disrupt at least articular cartilage and cortical bone,
said first elongated partially cylindrical section of said SI joint prosthesis comprising a first internal prosthesis engagement member lumen extending from said prosthesis proximal end, said first internal prosthesis engagement member lumen comprising a first threaded surface region,
said second elongated partially cylindrical section of said SI joint prosthesis comprising a second internal prosthesis engagement member lumen extending from said prosthesis proximal end, said second internal prosthesis engagement member lumen comprising a second threaded surface region,
said first and second internal prosthesis engagement member lumens adapted to receive said prosthesis guide pin and prosthesis engagement rod of said prosthesis deployment assembly therein,
said SI joint prosthesis further comprising a first plurality of slots, a second plurality of said first plurality of slots being in communication with said first internal prosthesis engagement member lumen and a third plurality of said first plurality of slots being in communication with said second internal prosthesis engagement member lumen,
said SI joint prosthesis being sized and adapted to be inserted into said pilot SI joint opening;
d. making an incision in and through tissue at an incision site on said subject to provide posterior access to said subject's dysfunctional SI joint;
e. advancing said guide pin of said tool assembly from a posterior approach in and through said incision and into said dysfunctional SI joint, wherein said guide pin is positioned in said dysfunctional SI joint at an angle in the range of 25°-35° relative to a cephalocaudal axis of said subject;
f. assembling a drill guide assembly, wherein said drill guide is positioned in an access sleeve of said drill guide assembly;
g. inserting said guide pin of said tool assembly into said drill guide assembly;
h. advancing said drill guide assembly along said guide pin into said dysfunctional SI joint;
i. creating said pilot SI joint opening with said drill guide assembly;
j retracting said drill guide from said access sleeve of said drill guide assembly, wherein said guide pin is also retracted out of said tool assembly;
k. retracting said drill guide from said dysfunctional SI joint;
l. connecting said SI joint prosthesis to said prosthesis deployment assembly, wherein said prosthesis guide pin is inserted into said first internal prosthesis engagement member lumen of said first elongated partially cylindrical section of said SI joint prosthesis and said threaded distal end of said prosthesis engagement rod is threaded into said second internal prosthesis engagement member lumen of said second elongated partially cylindrical section of said SI joint prosthesis;
m. advancing said SI joint prosthesis into said pilot SI joint opening with said prosthesis deployment assembly, wherein said SI joint prosthesis is disposed in said dysfunctional SI joint at least 3.0 mm away from said SI joint dorsal recess;
n. retracting said prosthesis deployment assembly out of said dysfunctional SI joint; and
o. retracting said access sleeve of said drill guide assembly out of said dysfunctional SI joint and out of said subject's body.