Granted Patent B2

US 12,484,945 · App. 18/329,231 · Granted Dec 2, 2025

Inventors: Michael Black (Phoenixville, PA); Damian Heinz (Wayne, PA)

Assignee: NEVRO CORP.

A61B17/92A61B17/025A61B17/1604A61B17/1659A61B17/1671A61B17/17A61B17/3468A61B17/1739A61B17/1757A61B2017/320044A61B2017/346A61B2017/922A61F2002/3093A61F2002/30995A61F2/4603A61F2002/4627A61F2002/4635A61F2002/4687

Abstract

Claims (43)

1 . A surgical system for preparing the sacroiliac (SI) joint for a fusion, comprising a sliding joint finder, a lateral guide boom and a working cannula;

a) wherein the sliding joint finder comprises:

i) a central axis with a hole that runs the length of the sliding joint finder;

ii) a unilateral shelf located on an outer surface of the sliding joint finder; and

b) wherein the working cannula comprises a body having a central axis that runs the length of the body;

wherein the body of the working cannula comprises a distal end, a proximal end and a central cavity that is positioned along the central axis of the working cannula and has suitable dimensions for sliding the working cannula over the sliding joint finder;

wherein the working cannula further comprises two protrusions extending proximally; and

wherein the two protrusions have uneven lengths such that when the working cannula is inserted into the SI joint over the sliding joint finder, the longer of the two protrusions is configured to engage the SI joint at a superior end of the SI joint and the shorter of the two protrusions is configured to engage the SI joint at an inferior end of the SI joint

wherein the lateral guide boom comprises a proximal end with a paddle shaped structure with one or more drill holes, configured to receive bone screws, a lateral arm configured to be inserted into a rectangular slot of the working cannula, and

wherein the lateral guide boom is configured to be locked to the working cannula with a threaded capture clip.

2 . The surgical system of claim 1 , further comprising an implant insertion tool, wherein the implant insertion tool comprises an elongated body and a slidable insertion ram;

wherein the body of the insertion tool comprises an insertion region and an insertion end, and a central cavity that runs along a central axis of the insertion tool;

wherein the slidable insertion ram comprises a body portion configured to be located within in the central cavity of the working cannula and in slidable relation thereto; and

wherein the insertion region and insertion end have suitable dimensions for insertion of a spacer implant into the working cannula.

3 . The system of claim 2 , wherein the insertion end of the body of the insertion tool comprises a flexible tab that can be deformed to retain one or more implants within the insertion end.

4 . The system of claim 3 , wherein the slidable insertion ram of the implant insertion tool is configured to push the implant(s) out of the insertion end and into the joint, when the insertion ram moves from a retracted position to an operative position.

5 . The system of claim 3 , wherein the insertion end of the implant insertion tool comprises a cavity configured to retain an implant, when the tab is deformed.

6 . The system of claim 1 , wherein the hole that runs the length of the sliding joint finder has suitable dimensions to slide over a wire or pin and allow for removal of the wire or pin from a surgical site through the sliding joint finder.

7 . The system of claim 1 , wherein the sliding joint finder has two lateral sides and a unilateral shelf located on only one of the lateral sides at a suitable location for contacting a shelf on the ilium, when the sliding joint finder is inserted into the SI joint with the lateral side having the unilateral shelf facing the ilium.

8 . The system of claim 1 , wherein the working cannula further comprises a unilateral shelf distal to the two protrusions.

9 . The system of claim 1 , further comprising one or more spacer implants.

10 . The system of claim 9 , wherein the one or more spacer implants is formed from a material selected from the group consisting of allograft, autograft bone, biocompatible metal, polymers, ceramics, and other synthetic materials.

11 . The system of claim 1 , wherein the cavity of the working cannula has substantially straight lateral walls.

12 . The system of claim 1 , further comprising one or more tools for preparing the SI Joint selected from the group consisting of drill guides and joint box chisels, wherein each of the tools has a proximal end, and wherein each of the tools has suitable dimensions for the proximal end of the tool to be inserted into the working cannula.

13 . The system of claim 1 , wherein the distal end of the working cannula is configured to receive a lateral guide for fixation elements.

14 . The system of claim 1 , wherein the cannula is configured such that when the cannula is inserted, each of the two protrusions engages the sacrum on one side of the protrusion and the ilium on the other side of the protrusion.

15 . The system of claim 1 , wherein the central cavity of the working cannula terminates at a proximal terminus; and

wherein the two protrusions of the working cannula extend proximally from the proximal terminus of the central cavity.

16 . The system of claim 8 , wherein a first distance from the longer of the two protrusions to the shelf is about 35 mm and a second distance from the shorter of the two protrusions to the shelf is about 15 mm.

17 . A surgical system for preparing the sacroiliac joint for a fusion, comprising a sliding joint finder and a working cannula;

a) wherein the sliding joint finder comprises:

i) a central axis with a hole that runs the length of the sliding joint finder;

ii) a unilateral shelf located on an outer surface of the sliding joint finder; and

b) wherein the working cannula comprises a body having a central axis that runs the length of the body;

wherein the body of the working cannula comprises a distal end, a proximal end and a central cavity that is positioned along the central axis of the working cannula and has suitable dimensions for sliding the working cannula over the sliding joint finder, the body including a first side and a second side that opposes the first side;

wherein the first side of the body of the working cannula includes a first marking configured to identify that the first side is configured to face the ilium and the second side of the body of the working cannula includes a second marking configured to identify that the second side is configured to face the sacrum, the second marking being different from the first marking;

wherein the working cannula further comprises a first protrusion and a second protrusion extending proximally; and

wherein the first protrusion is longer than the second protrusion such that when the working cannula is inserted into the SI joint over the sliding joint finder, the first side is configured to face the ilium, the second side is configured to face the sacrum, the first protrusion is configured to engage the SI joint at a superior end of the SI joint, and the second protrusion is configured to engage the SI joint at an inferior end of the SI joint,

wherein the lateral guide boom comprises a proximal end with a paddle shaped structure with one or more drill holes, configured to receive bone screws, a lateral arm configured to be inserted into a rectangular slot of the working cannula, and

wherein the lateral guide boom is configured to be locked to the working cannula with a threaded capture clip.

18 . The system of claim 17 , wherein the first marking is an “I”.

19 . The system of claim 17 , wherein the second marking is an “S”.

20 . The system of claim 17 , wherein the working cannula further comprises a unilateral shelf distal to the two protrusions, a first distance from the first protrusion to the shelf being about 35 mm and a second distance from the second protrusion to the shelf being about 15 mm.

Assignments (6)

Continuity (3)

References Cited (65)