Medtronic, Inc.

Cardiac Pacemakers, Inc.

Medtronic Xomed, Inc.

Adam J Rivard

Scott M Hanson

Joseph P Ricci

Jonathan C Sell

Phillip C Falkner

Sean Patrick Skubitz

Robert T Sandgren

Kevin E Verzal

Avram Scheiner

Stephen L Bolea

G Shantanu Reddy

David R Wulfman

James B Hissong

Thomas I Miller

David A Durand

Evan Mark Gustafson

Ryan R Davis

Vincent Whelan

Justin M Claus

Chad C Whiterabbit

Mary Bengtson

Leonid Michael Litvak

Richard T Stone

Bryan Allen Clark

Eric H Bonde

Andrew Cecil Harvey

Bernard Q Li

Brian T Stolz

Mohan Krishnan

Kanthaiah Koka

Jeffrey P Bodner

Kristin N Hageman

Edward Dickinson

Bruce A Behymer

Raymond F McMullen

Erik J Peterson

Christopher Alan Fuhs

David J Miller

Daniel J Cooke

Patsy Coppola

Seth M Humphrys

Douglas Scott Cerny

Kyle K Hoecke

Jeffrey R Dixon

John Shishilla

Jeevan M Prasannakumar

Charles Thomas Bombeck

Walton W Baxter

Darrin E Dickerson

Jorge Alvarado

Thomas J Steigauf

Joshua D Trevorrow

Ryan Kleve

Ryan B Sefkow

Vincent M Whelan

Implantable medical leads and/or lead extensions include a band that encapsulates a portion of conductors of the lead and/or lead extension. The band may be reflowed in order to provide the encapsulation of the conductors. The band may further be used to create a seal together with the surrounding lead body and an additional object such as a stiffener rod, stylet tube, and/or molding stylet, to allow a proximal area of a lumen of the lead body to be injection molded while prevent the injection molding material from proceeding past the band. When a stiffener rod is present in a proximal area of the lead and/or lead extension, additional stiffness is provided to the lead body to resist buckling of the lead body during insertion of the proximal end. The band may be bonded to the stiffener rod to fix the position of the stiffener rod relative to the conductors.

Implantable medical leads and lead extensions having an encapsulation band

A medical system for obstructive sleep apnea (OSA) treatment includes therapy delivery circuitry configured to output one or more electrical stimulation signals to a tongue of a patient; sensing circuitry configured to sense one or more compound muscle action potential (CMAP) signals, wherein the one or more CMAP signals are generated in response to the delivery of the one or more electrical stimulation signals; and processing circuitry configured to: cause the therapy delivery circuitry to output the one or more electrical stimulation signals to the tongue; receive information indicative of the one or more CMAP signals from the sensing circuitry; determine, based on the one or more CMAP signals, one or more therapeutic stimulation parameters for the OSA treatment; and cause the therapy delivery circuitry to deliver therapeutic electrical stimulation signals according to at least the determined one or more therapeutic stimulation parameters.

Stimulation therapy for treating obstructive sleep apnea (OSA) based on compound muscle action potential (CMAP)

A first medical device for obstructive sleep apnea therapy includes therapy delivery circuitry coupled to a first set of electrodes implantable proximate to a first hypoglossal nerve within a tongue of the patient and configured to deliver a first electrical stimulation signal to the first hypoglossal nerve that causes the tongue of the patient to advance and includes information to communicate to a second medical device implantable within the head or neck of the patient and coupled to a second set of electrodes implantable proximate to a second hypoglossal nerve within the tongue of the patient; and sensing circuitry coupled to the first set of electrodes and configured to receive a second electrical stimulation signal, delivered to the second hypoglossal nerve by the second medical device, that includes information that the second medical device communicates to the first medical device.

Multi-device obstructive sleep apnea (OSA) treatment

Implantable medical lead devices such as leads and lead extensions include conductors within the lead device body that interconnect proximal and distal electrical connectors and that have balanced clocked positions. The balanced clocked positions may be achieved by separating a first conductor from a second conductor by an adequate amount, where the first conductor has a length as measured from a given point along the lead to the end of the conductor that is most similar to the length of the second conductor as measured in the same manner. The balanced clocked position of conductor pairings based on similarity of length may provide benefits such as reducing the tendency of the lead to curve when one or more layers of the lead body are being injection molded around the conductors.

Implantable medical lead devices and systems having balanced clocked conductor positions

Distal connector assemblies that are on the distal end of medical lead extensions provide increased rigidity by including a rigid holder that contains the electrical connectors. The electrical connectors are separated within the rigid holder by insulative spacers that may be individual items or may be formed from a compliant carrier that the electrical connectors may reside within where the carrier is positioned within the rigid holder. The rigid holder may also contain a set screw block defining set screw bore or the rigid holder may include an integral portion that defines a set screw bore. The integral portion may include a slot to allow a molding pin loaded with the electrical connectors and other components to be dropped into a cavity of the rigid holder. An overmold may be present to surround the rigid body containing the electrical connectors and insulative spacers.

Distal connector assemblies for medical lead extensions

A temporary medical electrical lead includes a connector pin and a single conductor coil. The coil being close-wound and having no turns of the coil distal portion being mechanically coupled together. The coil distal portion translates a force of no greater than 0.1 lb(0.4 N) when strained 400%.

Implantable medical electrical lead construction and associated implant systems

Tips for use on a tunneling tool provide the ability to pull an implantable medical lead extension or catheter body through a subcutaneous tunnel. The tips may include a pin with a barb, where the barb is inserted within a compliant portion of a connector body of the lead extension or a catheter body to create an interference fit that allows the connector body or catheter body to be pulled through the tunnel. The tips may include a carrier that has a cavity for the connector body, where the tunneling is performed with the carrier present on the tunneling tool. A body is positioned within the cavity of the carrier to prevent tissue from snagging on and collecting within the carrier. The body may include a tip portion that performs the tunneling function. The carrier may also provide tunneling and/or may be attached to the tunneling tool during tunneling.

Tools and methods for implantation of implantable medical lead extensions or catheters

Kits provide management of implantable lead extensions being implanted by providing a kit body with features that retain the extension in a configuration, with amounts being removed as needed during the implantation procedure. The kit can be present within a sterile field, and the kit body features may be arranged so that a length of a path that the extension forms is approximately equal to a length of the extension needed for the tunnel. The kit body may include features that allow the connectors of the extension as well as implantation tools to be retained within the kit body while being easily accessed when needed during the procedure. The kit may be coupled to the patient during the trial period, as the extension may have an implanted distal connector while having a proximal connector coupled to an external stimulator and while being retained on the kit body.

Kits and methods for implanting an implantable lead extension

An implantable lead includes a flexible lead body, a plurality of conductor wires and a plurality of electrodes. The implantable lead also includes a terminal connector assembly coupled with a proximal end of the lead body. The terminal connector assembly is sized to be inserted into and received by a connector port of a pulse generator header. The terminal connector assembly includes a plurality of axially spaced terminal ring elements each electrically coupled to at least one of the conductor wires. The terminal ring elements are separated from one another by an electrically insulating material. Each of the terminal ring elements includes an outer surface having a first portion and a second portion, the first portion being electrically conductive and the second portion being electrically non-conductive.

Terminal ring configuration to prevent improper IS4 lead connector electrical contact with DF4 connector port

Growing community of inventors

Blaine, MN, United States of America

Adam J Rivard