Medtronic, Inc.

Medtronic Ablation Frontiers LLC

Medtronics, Inc.

Jonathan L Kuhn

Can Cinbis

James Kevin Carney

David A Anderson

Thomas A Anderson

Vladimir Grubac

Kenneth D Rys

Richard W Swenson

James D Reinke

Richard J O'Brien

Timothy J Davis

Michael P Campbell

Rodolphe Katra

Jonathan P Roberts

Jeffrey M Jelen

Saul E Greenhut

Charles Lowell Wilson

Yong Kyun Cho

John E Burnes

William John Havel

Robert Michael Ecker

Jesper Svenning Kristensen

Xiaonan Shen

Mark J Phelps

Avram Scheiner

David Jerome Peichel

Thomas J Mullen

Mark R Boone

Michael B Terry

Kamal Deep Mothilal

James W Busacker

Shawn D Knowles

Andrew J Ries

Eduardo N Warman

Shantanu Sarkar

Vinod Sharma

Tommy Dean Bennett

Todd M Zielinski

Brian Bruce Lee

Paul F Gerrish

Tom Dean Bennett

Taylor R Anderson

Richard J O'BRIEN

A fixation component includes tines extending from a base portion of the fixation component. Each tine is elastically deformable between a pre-set position and an open position. Each tine includes a hook segment extending from a proximal end near the base portion to a distal end. Each tine also includes a distal segment extending from the distal end of the hook segment to a tissue-piercing tip. When positioned in the pre-set position, the hook segment extends along a pre-set curvature that encloses an angle between 135 degrees and 270 degrees, and the distal segment extends away from a longitudinal axis of the fixation component.

Fixation for implantable medical devices

In some examples, a medical system includes a medical device. The medical device may include a housing configured to be implanted in a target site of a patient, a light emitter configured to emit a signal configured to cause a fluorescent marker to emit a fluoresced signal into the target site, and a light detector that may be configured to detect the fluoresced signal. The medical system may include processing circuitry configured to determine a characteristic of the fluorescent marker based on the emitted signal and the fluoresced signal. The characteristic of the fluorescent marker may be indicative of a presence of a compound in the patient, and the processing circuitry may be configured to track the presence of the compound of the patient based on the characteristic of the fluorescent marker.

Marker monitoring via a medical device

This disclosure is related to devices, systems, and techniques for performing patient parameter measurements. In some examples, a medical device system includes an optical sensor configured to measure ambient light and a tissue oxygen saturation parameter and processing circuitry configured to determine that a current measurement of the tissue oxygen saturation parameter is prompted and control the optical sensor to perform an ambient light measurement associated with the current measurement of the tissue oxygen saturation parameter. The processing circuitry is further configured to determine, based on the ambient light measurement, at least one of whether to control the optical sensor to perform the current measurement of the tissue oxygen saturation parameter, when to control the optical sensor to perform the current measurement of the tissue oxygen saturation parameter, or whether to include the current measurement of the tissue oxygen saturation parameter in a trend of the tissue oxygen saturation parameter.

Performing measurements using sensors of a medical device system

Systems, devices, and techniques for establishing communication between two medical devices are described. In one example, an implantable medical device comprises communication circuitry, therapy delivery circuitry, and processing circuitry configured to initiate a communication window during which the implantable second medical device is capable of receiving the information related to a cardiac event detected by a first medical device, the communication window being one of a plurality of communication windows defined by a communication schedule that corresponds to a transmission schedule in which the first medical device is configured to transmit the information, control the communication circuitry to receive, from the first medical device, the information related to the cardiac event that is indicative of a timing of the cardiac event with respect to a timing of the communication window, schedule and control delivery of a therapy according to the information related to the cardiac event.

Low power wireless communication

A tine portion of an implantable medical device includes a hook segment and a distal segment terminated by a tissue-piercing tip, wherein the distal segment extends from a distal end of the hook segment to the tip. The hook segment, which is elastically deformable from a pre-set curvature, for example, defined by a single radius, preferably tapers from a first width thereof, in proximity to a proximal end thereof, to a smaller, second width thereof, in proximity to the distal end thereof, wherein the tip has a width that is greater than the second width of the hook segment. Alternately, the tine portion may include a hook segment that is defined by two radii and a straight section extending therebetween.

Various embodiments of a sealed package and a method of forming such package are disclosed. The package includes a housing, a substrate hermetically sealed to the housing, and a light source disposed on a first major surface of the substrate. The package further includes a detector disposed on the first major surface of the substrate and having a detecting surface. The package also includes a masking layer disposed on at least one of the first major surface and a second major surface of the substrate, where the masking layer includes a first aperture aligned with an emission axis of the light source in a direction orthogonal to the first major surface of the substrate. The masking layer further includes a second aperture aligned with a detection axis of the detector in a direction orthogonal to the first major surface of the substrate.

Hermetically-sealed package and method of forming same

In some examples, determining a health status includes using an implantable medical device configured for subcutaneous implantation and comprising at least one optical sensor. Processing circuitry of a system comprising the device may determine, for a patient, a current tissue oxygen saturation value based on a first signal received from the at least one optical sensor and a current pulsatile oxygen saturation value based on a second signal received from the at least one optical sensor. The processing circuitry may further compare the current tissue oxygen saturation and current pulsatile oxygen saturation values to corresponding baseline values, determine corresponding heart failure and pulmonary statuses of the patient based on the comparisons, and determine the health status of the patient based on the statuses.

Sensing for health status management

Various embodiments of a hermetically-sealed package and a method of forming such package are disclosed. The package can include a housing having an inner surface and an outer surface, and a non-conductive substrate hermetically sealed to the housing. The package can also include a light source disposed on a first major surface of the substrate and adapted to emit light through the first and second major surfaces of the substrate, and a detector disposed on the first major surface of the substrate and adapted to detect the light emitted by the light source.

A fixation member component, for example, employed by a relatively compact implantable medical device, includes a plurality of fingers; each finger includes a first segment extending from a fixed end of the corresponding finger, and a second segment extending from the corresponding first segment to a free end of the corresponding finger. Each first segment is elastically deformable from a relaxed to an extended condition, and from the relaxed to a compressed condition, and includes a peripheral portion and a central cut-out portion, framed by the peripheral portion. In the compressed condition, a free tip of the cut-out portion of some or all of the fingers may lodge against opposing tissue surfaces, via a spring force of the compressed fingers. Each second segment and cut-out portion is preferably configured to prevent penetration thereof within tissue at the implant site.

Interventional medical systems, devices, and components thereof

Growing community of inventors

Ham Lake, MN, United States of America

Jonathan L Kuhn