Abstract: An implantable medical device (IMD) may be deployed within a patient's right atrium at a location near a right atrial appendage of the patient's heart in order to pace the patient's heart and/or to sense electrical activity within the patient's heart. In some cases, an IMD may be implanted within the right atrial appendage. The IMD may include an expandable anchoring mechanism configured to secure the IMD in place.

Abstract: Delivery devices, systems, and methods for delivering implantable leadless pacing devices are disclosed. An example delivery device may an outer tubular member and an inner tubular member slidably disposed within the lumen of the outer tubular member. A distal holding section may extend distally of a distal end of the inner tubular member and define a cavity therein for receiving an implantable leadless pacing device. The device may further include a hub portion including at least a first hub portion affixed adjacent to the proximal end of the outer tubular member and a second hub portion affixed adjacent to the proximal end of the inner tubular member. A first locking mechanism configured to releasably couple the outer tubular member and the inner tubular member may be disposed within the hub portion.

Abstract: An implantable leadless cardiac pacing device and associated retrieval features. The implantable device includes a docking member extending from the proximal end of the housing of the implantable device including a covering surrounding at least a portion of the docking member configured to facilitate retrieval of the implantable leadless cardiac pacing device.

Abstract: Systems and methods for conducted communication are described. In one embodiment, a method of communicating with a medical device implanted within a patient comprises receiving, at a medical device via electrodes connected to the patient, a conducted communication signal, wherein the conducted communication signal comprises a signal component and a noise component. The method may further comprise adjusting, by the medical device, a receive threshold based at least in part on an amplitude of the received conducted communication signal so as to reduce an amplitude of the noise component of the conducted communication signal.

Abstract: An implantable leadless cardiac pacing device and associated retrieval features. The implantable device includes a docking member extending from the proximal end of the housing of the implantable device including a covering surrounding at least a portion of the docking member configured to facilitate retrieval of the implantable leadless cardiac pacing device.

Abstract: This disclosure concerns systems and methods for tissue volume reduction and control of the flow of substances through the body. Systems according to the various embodiments of the disclosure include check valves formed from wire coils which are deployable through a tubular lumen, such as the working channel of an endoscope, or a catheter.

Abstract: A device configured to deliver and deploy an implantable medical device (IMD) includes a handle assembly and a shaft extending distally therefrom. A device containment housing configured to accommodate the IMD is coupled to the distal region of the shaft. At least one of the shaft and device containment housing includes a compressible region that is configured to compress by an amount that is related to an applied force. The device may include a first position indicator and a second position indicator. An applied force causes the compressible region to compress by an amount that is related to the applied force, causing a change in distance between the first position indicator and the second position indicator and thus providing an indication of the applied force.

Abstract: Exemplary embodiments of devices and methods for treating a lung including, for example, treatments for chronic obstructive pulmonary disease are disclosed. A device may include a plurality of media and a deployment member. The media may be configured for deployment into one or more airways of a lung. The deployment member may be configured for insertion into or proximate the one or more airways of the lung. Also, the deployment member may be configured to deploy the plurality of media substantially simultaneously. Further, the plurality of media may be configured to be retained within the one or more airways of the lung.

Abstract: A retrieval device and an associated implantable cardiac pacing device. The retrieval device includes a retrieval catheter and a snare advanceable from the distal end of the retrieval catheter. The snare has a loop configured to be coupled to the docking member to draw the implantable cardiac pacing device into the lumen of the retrieval catheter. The retrieval catheter includes a retention feature in the lumen configured to engage the head portion of the docking member to facilitate retention of the implantable cardiac pacing device in the lumen after drawing the implantable cardiac pacing device into the lumen of the retrieval catheter with the snare.

Abstract: A lung device for restoring lung elasticity includes fixation members and a connecting member. The fixation member includes a first radially expandable fixation member and a second radially expandable fixation member. The first radially expandable fixation member defines a first profile in an expanded state and a lumen. The second radially expandable fixation member defines a second profile in an expanded state and a lumen. The connecting member extends between and connects the first and second fixation members. The lung elasticity restoring device is capable of reversibly extendable between an inspiration configuration and an expiration configuration, may be extendable to the inspiration configuration, and biased to the expiration configuration by the connecting member.

Abstract: A method for treating a lung may include forming a channel between a first airway and a second airway through a tissue of the lung to allow air trapped within the first airway to flow through the channel and the second airway, and inserting a support member into the channel.

Abstract: An implantable medical device for implantation into a patient may include a housing, a pulse generation circuit disposed at least partially within the housing, a plurality of electrodes electrically coupled to the pulse generation circuit, the plurality of electrodes being exposed external to the housing, and a controller operatively coupled to the pulse generation circuit. The controller may be configured to command the pulse generation circuit to deliver a phasic conducted communication pulse via at least two of the plurality of electrodes. Additionally, the phasic conducted communication pulse may comprise a first phase having a first polarity followed by a second phase having an opposite second polarity, wherein the second phase may have a duration of less than 60 microseconds, and wherein the first phase having may have a duration of between five percent and eighty percent of the duration of the second phase.

Abstract: Delivery devices, systems, and methods for delivering implantable leadless pacing devices are disclosed. An example delivery device may include an intermediate tubular member and an inner tubular member slidably disposed within a lumen of the intermediate tubular member. A distal holding section may extend distally of a distal end of the intermediate tubular member and define a cavity therein for receiving an implantable leadless pacing device. The device may further include a handle assembly including at least an intermediate hub portion affixed adjacent to the proximal end of the intermediate tubular member and a proximal hub portion affixed adjacent to the proximal end of the inner tubular member. A longitudinally extending groove having a proximal end and a distal end may be disposed in the intermediate hub portion. A first locking mechanism may be configured to releasably couple the intermediate hub portion and the proximal hub portion.

Abstract: Delivery devices, systems, and methods for delivering implantable leadless pacing devices are disclosed. An example delivery system may comprise a delivery device, an implantable leadless pacing device, and a tether. The tether may be made of a material which allows for a lubricious, strong, no stretch, no memory tether. The tether may releasably secure the implantable leadless pacing device to the delivery device.

Abstract: Fixation mechanism assemblies and methods are disclosed. A fixation mechanism assembly can include a first fixation member and a second fixation member moveably engaged with the first fixation member. The first fixation member can include a housing having a tissue facing surface and an opposing non-tissue facing surface, one or more guide apertures extending between the tissue facing surface and the non-tissue facing surface, and one or more first fixation elements. The first fixation member includes a longitudinal body and a proximal end attached to, or integrated with, the tissue facing surface of the housing. The second fixation member can include one or more second fixation elements. The second fixation element can correspond to a guide aperture and includes a longitudinal body, a proximal end attached to, or integrated with, the second fixation member, and a distal end movable through the corresponding guide aperture.

Abstract: One aspect provides a capacitor feedthrough assembly having an electrically conductive member dimensioned to extend at least partially through a feedthrough hole of a case of the capacitor, the conductive member having a passage therethrough.

Abstract: Systems, methods, and devices for detecting or confirming fibrillation are discussed. In one example, a method for detecting a cardiac arrhythmia of a patients' heart comprises receiving, by a leadless cardiac pacemaker fixed in the patients' heart, an indication from a remote device that a cardiac arrhythmia is detected, monitoring by the leadless cardiac pacemaker a signal generated by a sensor that is located within the patients' heart, and based at least in part on the monitored signal, confirming whether a cardiac arrhythmia is occurring or not. In some embodiments, the method may further comprise, if a cardiac arrhythmia is confirmed, delivering a therapy to treat the cardiac arrhythmia.

Abstract: Systems, devices, and methods for adjusting functionality of an implantable medical device based on posture are disclosed. In some instances, a method for operating a leadless cardiac pacemaker implanted into a patient, where the patient has two or more predefined behavioral states, may include detecting a change in the behavioral state of the patient, and in response, changing a sampling rate of a sensor signal generated by a sensor of the leadless cardiac pacemaker. In some embodiments, the method may further include using the sampled sensor signal to determine an updated pacing rate of the leadless cardiac pacemaker and providing pacing to the patient at the updated pacing rate.

Abstract: Systems, methods, and devices for detecting dislodgment of an implantable device are disclosed. In one example, a method for determining a dislodgement status may comprise collecting, by the implantable device operating in a first operating mode, a first number of accelerometer signal samples during a cardiac cycle of the heart and using the first number of accelerometer signal samples to determine a first patient parameter and collecting, by the implantable device operating in a second operating mode, a second number of accelerometer signal samples during a cardiac cycle of the heart and using the second number of accelerometer signal samples to determine a dislodgment status of the implantable device, wherein the first number is smaller than the second number. In some further embodiments, the method may further include providing a notification of the dislodgment status to a remote device that is remote from the implantable medical device.

Abstract: Systems, devices, and methods for determining occurrences of myocardial infarctions are disclosed. In one embodiment, a method of sensing for an occurrence of a myocardial infarction may include sensing a baseline accelerometer signal during a baseline, determining a baseline template based on one or more characteristics of the baseline accelerometer signal, and storing the baseline template in a memory. The method may further include sensing an accelerometer signal during a test period subsequent to the baseline, determining a test template based on one or more characteristics of the accelerometer signal during the test period, and comparing the baseline template with the test template, and based on the comparison, determining if a myocardial infarction occurred in the patient's heart. If it is determined that a myocardial infarction occurred in the patient's heart, the method may further include displaying an indication on a display that a myocardial infarction occurred.