Abstract: A rotational intravascular ultrasound probe for insertion into a vasculature and a method of manufacturing the same. The rotational intravascular ultrasound probe comprises an elongate catheter having a flexible body and an elongate transducer shaft disposed within the flexible body. The transducer shaft comprises a proximal end portion, a distal end portion, a drive shaft extending from the proximal end portion to the distal end portion, an ultrasonic transducer disposed near the distal end portion for obtaining a circumferential image through rotation, and a transducer housing molded to the drive shaft and the ultrasonic transducer.

Abstract: The invention provides an imaging device for use in medical interventions, such as surgery, comprising: an ultrasound probe to provide first image data; a cannula having a longitudinal internal channel and configured to be introduced into the human body; a direct vision camera arranged, at least partially, on or in the cannula to provide second image data; and a display device comprising at least one display to display an ultrasound image on the basis of the first image data and a direct vision image on the basis of the second image data.

Abstract: Various methods and systems are provided for a guided at-home ultrasound imaging session. In one example, a system for ultrasonically scanning a tissue sample includes a hand-held ultrasound probe including a transducer array of transducer elements, a probe position tracking device including one or more position sensors coupled to the ultrasound probe, and a controller. The controller is configured to, during an imaging session, determine a position of the ultrasound probe relative to a target position based on position data collected by the probe position tracking device, and responsive to an indication that the ultrasound probe is at the target position, acquire image data with the transducer array.

Abstract: Provided is an ultrasonic transducer and a preparation method thereof. The ultrasonic transducer includes a housing. A piezoelectric layer is disposed in the housing and includes at least two piezoelectric array elements. A frequency interval between the piezoelectric array elements is 50 kHz to 1.2 MHz. An acoustic lens is disposed at a front end of the piezoelectric layer and is used for ensuring that the piezoelectric array elements having different frequencies have a common focus.

Abstract: Various methods and systems are provided for imaging system user interfaces. In one embodiment, a method comprises displaying, via a touchscreen, a first virtual button, displaying a menu comprising a plurality of virtual buttons corresponding to actions responsive to detecting a finger pressing the first virtual button via the touchscreen, performing an action responsive to the finger being released from the touchscreen at a second virtual button associated with the action, and updating the display of the first virtual button to indicate the action. In this way, an operator of an imaging system may easily access a potentially large plurality of imaging modes and actions relating to imaging via a touchscreen during a scan, thereby extending the operator's ability to control the ultrasound imaging system in a reduced amount of time.

Abstract: Provided is a technique for evaluating properties of a membranous tissue or a surface of the tissue in a biological body by ultrasonic waves. A method of the invention includes setting one or more measurement points on a surface of the biological tissue to be inspected; measuring, in a state in which an elastic wave propagates to the biological tissue, at least a surface wave of the elastic wave by measuring a displacement of the biological tissue at the measurement point by using an ultrasonic wave; and calculating an index value indicating physical properties of the biological tissue by using the measured displacement.

Abstract: Disclosed is a method and related systems comprising detecting a position of each of two or more targets in a volume to be imaged; generating and directing a single beam of ultrasound energy toward the volume by simultaneously focusing the single beam on each of the two or more the target positions; detecting the ultrasound energy from each of the two or more the target positions; and using the detected ultrasound energy to generate an image of the volume to be imaged. Such as generating a blood flow profile in a blood vessel.

Abstract: A method of operating an ultrasound diagnosis apparatus includes: acquiring a plurality of frequency band images respectively having different frequency bands based on an ultrasound signal corresponding to an object; determining weights respectively for the plurality of frequency band images based on brightness levels of regions including the object in each of the plurality of frequency band images; synthesizing the plurality of frequency band images based on the weights for the plurality of frequency band images; and displaying a synthetic ultrasound image of the object, generated as a result of the synthesizing.

Abstract: Ultrasound imaging system, devices, and methods for minimizing grating lobe artefacts in an ultrasound image are provided. For example, an ultrasound imaging system can include an array of acoustic elements and a processor in communication with the array. The processor controls the array to activate a plurality of apertures and subapertures in a scan sequence, generate an image comprising a plurality of pixels, identify at least one subaperture of the plurality of subapertures corresponding to a reduced signal value for one or more pixels of the image, and generate a grating-lobe-minimized image based on the identified subapertures. The grating-lobe-minimized image can be output to a display or combined with the original ultrasound image to include image features lost or reduced in the grating-lobe-minimized image. The grating-lobe-minimized image advantageously reduces image artefacts and clutter to simplify ultrasound image analysis and diagnosis procedures.

Abstract: Aspects of present disclosure relates to information and control terminals for ultrasonic diagnostic systems and the ultrasonic diagnostic systems. In certain embodiments, ultrasonic diagnostic system includes: an information and control terminal, a local host in a first location, a remote host connected to an ultrasonic diagnostic imaging system in a second location, and a communication network. Information and control terminal is operated by an ultrasonic diagnostic expert located in first location. Information and control terminal retrieves patient information of a patient from patient database, provides ultrasonic diagnostic control instructions from ultrasonic diagnostic expert to ultrasonic diagnostic technicians in second location. An ultrasonic diagnostic technician performs ultrasonic diagnostic examination on patient according to ultrasonic diagnostic control instructions and transmits patient ultrasonic diagnosis information back to local host and ultrasonic diagnostic expert in real time.

Abstract: Aspects of present disclosure relates to ultrasonic diagnostic systems. In certain embodiments, ultrasonic diagnostic system includes: a local host in a first location, a mobile information and control terminal, a remote host connected to an ultrasonic diagnostic imaging system in a second location, and a communication network. The mobile information and control terminal is operated by an ultrasonic diagnostic expert located in the first location. The mobile information and control terminal retrieves patient information of a patient from patient databases, provides ultrasonic diagnostic control instructions from ultrasonic diagnostic expert to ultrasonic diagnostic technicians in second location. An ultrasonic diagnostic technician performs ultrasonic diagnostic examination on patient according to the ultrasonic diagnostic control instructions and transmits patient ultrasonic diagnosis information back to the local host and the ultrasonic diagnostic expert in real time.

Abstract: Aspects of present disclosure relates to mobile information and control terminals for ultrasonic diagnostic systems and the ultrasonic diagnostic systems. In certain embodiments, ultrasonic diagnostic system includes: a mobile information and control terminal, a local host in a first location, a remote host connected to an ultrasonic diagnostic imaging system in a second location, and a communication network. Mobile information and control terminal is operated by an ultrasonic diagnostic expert in the first location. Mobile information and control terminal retrieves patient information of a patient from patient database, provides ultrasonic diagnostic control instructions from ultrasonic diagnostic expert to ultrasonic diagnostic technicians in second location.

Abstract: A distributed patient monitoring system comprises at least one standalone portable ultrasound imaging unit configured to be fixed to a stable position against the skin on a patient's body and capable of prolonged ultrasound data acquisition, including an ultrasound imaging array, transmit-receive circuitry, a beamformer, backend signal and image processing subsystem, power and communication subsystems, and a monitoring workstation connected to each standalone portable ultrasound imaging unit configured to request and receive ultrasound imaging information from each standalone portable ultrasound imaging unit, and configured to analyze and display acquired ultrasound information.

Abstract: Aspects of present disclosure relates to ultrasonic diagnostic systems. In certain embodiments, ultrasonic diagnostic system includes: a local host connected to an information and control terminal located in a first location, a remote host connected to an ultrasonic diagnostic imaging system in a second location, and a communication network. The information and control terminal is operated by an ultrasonic diagnostic expert located in the first location. The information and control terminal retrieves patient information of a patient from patient databases, provides ultrasonic diagnostic control instructions from ultrasonic diagnostic expert to ultrasonic diagnostic technicians in second location. An ultrasonic diagnostic technician performs ultrasonic diagnostic examination on the patient according to the ultrasonic diagnostic control instructions and transmits patient ultrasonic diagnosis information back to the local host and the ultrasonic diagnostic expert in real time.

Abstract: Urinary tract infections UTI may be over-diagnosed in very young children because of contamination of a urine specimen by external bacteria when using a conventional catheter. The subject matter disclosed herein relates to a coaxial catheter system and methods for its use, comprising an outer catheter that shields the distal collection opening of an inner catheter during insertion of the system through the meatus. Once the system has been deployed, the distal opening of the inner catheter is exposed in order to collect uncontaminated urine. The system may include a variety of mechanisms to advance the inner catheter relative to the outer, or to retract the outer catheter relative to the inner, a halting mechanism to limit distal movement of the outer catheter, a stopping mechanism to limit distal movement of the inner catheter, and a stabilization mechanism to hold the deployed system in place in male patients.

Abstract: A biopsy device (100), comprising: a cannula (102) comprising an elongate cannula body (106) extending between a cannula distal end (108) and a cannula proximal end (110) to define a lumen (112), wherein the cannula comprises a cutting portion at the cannula distal end (108); a stylet (104) comprising an elongate body (116) having a stylet distal end (118) and a stylet proximal end (120), the stylet (104) being slidably disposed within the lumen (112), wherein the stylet (104) comprises a tissue sampling portion (122); and an alignment means (126) arranged to maintain a preferred alignment between the stylet (104) and the cannula (102), wherein the alignment means (126) is arranged to align one or more of: i) relative rotation between the stylet distal end and the cannula distal end; ii) relative flexing between the stylet distal end and the cannula distal end; and iii) relative axial translation between the stylet distal end and the cannula distal end.

Abstract: An impact biopsy device is disclosed. The impact biopsy device may be configured to displace various cutting elements, such as an outer tubular member and cutting element and a cannula to sever a tissue sample from a patient. The impact biopsy device may comprise an actuation system configured to transfer displacement or force to the cutting elements by the impact of an element on another element.

Abstract: A biopsy apparatus includes a biopsy probe assembly that is releasably attached to a driver assembly. The biopsy probe assembly has a vacuum cannula and a stylet cannula coaxially arranged. The vacuum cannula has a flared portion that extends distally from an elongate portion. The stylet cannula is movable between a first extended position and a first retracted position. The stylet cannula has a distal portion having a sample notch and a protrusion member that extends proximally in a lumen of stylet cannula along a portion of a longitudinal extent of the sample notch, wherein when the stylet cannula is in the first retracted position, the protrusion member is received within the flared portion of the vacuum cannula. The biopsy apparatus may further include a controller circuit that has a virtual energy reservoir, and the controller circuit executes program instructions to control current to motors when engaging dense tissue.

Abstract: A tissue collection device (1) for collection of one or more exposed tissue samples (2) from a biopsy needle or biopsy device, which tissue collection device comprises one or more pieces of a carrier medium (6) and is arranged to temporarily bring a piece of carrier medium into physical contact with the tissue sample, while the tissue sample is still positioned in the biopsy needle or biopsy device, so that the tissue sample (2) adheres to the carrier medium (6) and is removed from the biopsy needle (3) or biopsy device (4) with the carrier medium (6), when the carrier medium (6) is removed from the biopsy needle or biopsy device again. Furthermore, a biopsy device comprising such a tissue collection device is disclosed.

Abstract: A tissue holder assembly for receiving and imaging severed tissue samples from a biopsy device includes a base and a cover removably attached to the base to define an interior, the base having one or more vacuum lumens in communication with the interior, the assembly further including a tissue tray removably and rotatably mounted in the interior, wherein a bottom of the tissue tray comprises a filter material that allows fluid to pass through. The cover has a tissue sample entry port formed therein and configured direct severed tissue samples and fluid aspirated therethrough into a respective tissue storage compartment of the tissue tray positioned under the tissue sample entry port, wherein the base includes a raised surface underlying at least a portion of the tissue tray circumferentially spaced apart from the tissue sample entry port when the cover is attached to the base.

Abstract: An apparatus includes an occlusion device operable to fit securely in an anatomical passageway within a head of a human. The occlusion device is configured to move unitarily with the head when the occlusion device is installed in the anatomical passageway. The occlusion device is further configured to prevent passage of fluid through the anatomical passageway when the occlusion device is installed in the anatomical passageway. A position sensor is fixedly integrated into the occlusion device. The position sensor generates signals indicating a position of the occlusion device in three-dimensional space, thereby indicating the position of the head in three-dimensional space. A connector communicatively coupled to the position sensor is operable to receive and transmit the signals generated by the position sensor.

Abstract: The present disclosure relates, in part, to a scanning sufficiency apparatus that computes whether a handheld scanning device has scanned a volume for a sufficiently long time for there to be detections and then indicate to the user that the time is sufficient in 3-D rendered voxels. Also described is a hand held medical navigation apparatus with system and methods to map targets inside a patient's body.

Abstract: The present disclosure provides an articulation joint that can include a plurality of articulation links, wherein each articulation link can include an elongate body having a proximal end, a distal end, an outer surface, and a first lumen extending from the proximal end to the distal end. Each articulation link can further include a plurality of arms extending radially outward from the elongate body, wherein each arm includes an inner end attached to the outer surface of the elongate body and a second lumen extending from a proximal side of the arm to a distal side of the arm. The articulation joint can also include a bending member positioned within the first lumen of the elongate body and a control member positioned within a plurality of second lumens, wherein each of the plurality of second lumens includes a common longitudinal axis.

Abstract: A pedicle screw mounted retractor has a split tube body that has a central tube longitudinally split into two split halves, a first half portion and a second half portion. The split halves form a central working portal. Each half portion has a cylindrical retractor tube appended on a side along an external surface. Each cylindrical retractor tube has a flange with a post extending at or near a proximal end. The pair of cylindrical retractor tubes is configured to pass onto and over a tower or extended top threaded post of a pedicle screw prepositioned in a pair of vertebrae for retracting the vertebrae. The central working portal has at least a 20 mm diameter in a closed and abutted orientation of the first and second split halves. In one embodiment, the central working portal has a 22 mm diameter in the closed and abutted orientation.

Abstract: The present disclosure can include a system including a surgical arm, a retractor connected to the surgical arm, a force sensor mounted on the surgical arm, the force sensor configured to receive sensor data indicating force on the retractor from the force sensor, and a magnetorheological fluid actuator for actuating the surgical arm, the actuator configured to actuate according to the received sensor data, and adjust the surgical arm according to the received sensor data so as to maintain a constant retraction force. The present disclosure can additionally include a method for retracting tissue including applying force to the tissue with a magnetorheological fluid actuator to induce a retraction force, sensing a change in force applied to the tissue using a force sensor, and maintaining the retraction force by adjusting the force applied to the tissue.

Abstract: A surgical retractor adapted to develop the interval between the gastrocnemius and soleus to facilitate one or both of gastrocnemius and soleus recession to treat equinus is disclosed. Particular forms of the present disclosure include a retractor having handles extending transversally to the retractor head such that the handles may be used to manipulate and actuate the instrument with its head positioned through an incision and into the interval between the gastrocnemius and soleus, with the handles extending either distally or proximally from the incision site so that such handles do not interfere with the surgical procedure. In other illustrative embodiments, the retractor head can include a gastrocnemius retractor and a soleus retractor, each of which include a plurality of guides operable to guide the incision of the fascial layer of the gastrocnemius and soleus, respectively, to effect intermuscular fascial lengthening to relieve equinus.

Abstract: Systems, devices and methods for dilating and/or expanding the iris of a patient's eye during eye surgery is disclosed, comprising an elastomeric ring made from biocompatible material having a groove formed therein for receiving and protecting the pupillary rim and iris, whereby, when the ring is inserted into the pupil of an eye of a patient, it mechanically dilates the pupil.

Abstract: Devices, systems and methods for compressing, cutting, incising, reconfiguring, remodeling, attaching, repositioning, supporting, dislocating or altering the composition of tissues or anatomical structures to alter their positional or force relationship to other tissues or anatomical structures. In some applications, the invention may be used to used to improve patency or fluid flow through a body lumen or cavity (e.g., to limit constriction of the urethra by an enlarged prostate gland).

Abstract: A method and apparatus for coupling a soft tissue implant into a locking cavity formed within a bone is disclosed. The apparatus includes a member to pull the soft tissue implant into a femoral tunnel. The member includes a suture having first and second ends which are passed through first and second openings associated with the longitudinal passage to form a pair of loops. Portions of the suture lay parallel to each other within the suture, Application of tension onto the suture construction causes retraction of the soft tissue implant into the femoral tunnel.

Abstract: A method and apparatus for coupling a soft tissue implant into a locking cavity formed within a bone is disclosed. A bone engaging fastener is coupled to bone. A second fastener is coupled to a suture construction. The second fastener is coupled to the first fastener. Soft tissue is coupled to the suture construction.

Abstract: A tissue repair apparatus includes a housing, a rotatable shaft at least partially disposed within the housing, and first and second curved needles coupled to the shaft. The housing defines a gap between a first edge of the housing and a second edge of the housing, the gap adapted to receive tissue. The first and second needles curved needles being articulable within the housing from a delivery position, at which the first and second needles are spaced from the gap, to a deployed position, at which the first and second needles extend through the gap. Actuation of the shaft simultaneously articulates the first and second needles and the first needle enters the gap before the second needle enters the gap.

Abstract: Suturing devices and systems used to close openings into a biological structure. The suturing device can comprise an elongate member having a proximal end, a distal end, one or more arms, and one or more needles. One or more sheaths may be used with the device to maintain or substantially maintain haemostasis while the device is used and while a procedure is performed in the biological structure.

Abstract: A surgical stapling apparatus includes an actuating device including an elongated shaft. A tool assembly is disposed on a distal end of the shaft. The tool assembly includes a first jaw member supporting a cartridge assembly having a plurality of surgical fasteners, and a second jaw member supporting an anvil. The first jaw member is movable in relation to the second jaw member between a spaced position and an approximated position. One of the first or second jaw members includes a cantilever at a proximal end thereof. A firing cam bar assembly is slidably disposed within the tool assembly and includes a cam surface configured to engage the cantilever to move the first and second jaw member towards the approximated position and a distal end configured to deploy the plurality of surgical fasteners from the cartridge assembly.

Abstract: A surgical apparatus is provided. The surgical apparatus includes an actuator device including a body portion defining a longitudinal axis and a first articulating link. The first articulating link includes a mechanical interface and is movable between a non-articulated position and at least one articulated position. A reload is releasably coupled to a distal end of the body portion. The reload including a second articulating link configured to engage the first articulating link when the reload is coupled to the actuator device. The reload including a tool assembly which is pivotable from a first a position aligned with the longitudinal axis of the body portion to at least one position misaligned with the longitudinal axis of the body portion. The first articulation link and the mechanical interface prevent the reload from being disengaged from the actuator device when the first articulating link is in the at least one articulated position.

Abstract: An end effector includes an anvil and a cartridge assembly having a plurality of surgical staples disposed in a cavity defined therein. The cartridge assembly may include a movable driver or sled configured to deploy the surgical staple from the cavity into tissue. The surgical staple may include a linear leg and an arcuate leg extending therefrom. The linear leg may include a protruding portion to provide pressure to tissue captured by the surgical staple. A three-dimensional and/or self-supporting surgical staple may interlock its two legs upon deployment thereof.

Abstract: A surgical instrument includes an elongated shaft and an end effector coupled to the shaft. The end effector includes a first member, a knife member, and a second member. The first member is movable towards a distal end of the end effector. The knife member is pivotally coupled to the first member. The second member is movable towards the distal end of the end effector. The knife member is configured to be in a cutting position during a translation of the first and second members towards the distal end of the end effector. The knife member is rotatable relative to the first member to stow the knife member into a non-cutting position after the translation of the first and second members towards the distal end of the end effector.

Abstract: A buttress assembly is configured to temporarily adhere to a wet surgical stapler end effector. The buttress assembly includes a buttress body and a humidity tolerant adhesive material. The humidity tolerant adhesive material is applied to at least one side of the buttress body. The humidity tolerant adhesive material is configured to hold the buttress body to an underside of an anvil or a deck of a staple cartridge for at least five minutes in an environment of 100% relative humidity at approximately 37° C.

Abstract: A surgical stapling device for sequentially applying a plurality of fasteners to body tissue and simultaneously incising tissue is provided. The surgical stapling device is adapted to receive disposable loading units having staples in linear rows whose length can be between about 30 mm and 60 mm. The disposable loading unit includes a proximal body portion, a mounting assembly and a tool assembly. The mounting assembly is secured to the proximal end of the tool assembly and pivotally mounted about a pivot axis to the distal end of the proximal body portion. A support member or blow-out plate assembly is positioned on opposite sides of the pivot axis and extends between the proximal body portion and the mounting assembly.

Abstract: The present disclosure describes interventional devices, systems, and methods for closing a regurgitant gap in a cardiac valve. Interventional devices are configured to be deployed between two previously placed implants or between a previously placed implant and a valve commissure. The interventional devices compress captured leaflet tissue and/or apply a tensioning force along the line of coaptation to assist in closing the gap and reducing regurgitant flow through the gap.

Abstract: A fastener cartridge can comprise a support portion, a tissue thickness compensator positioned relative to the support portion, and a plurality of fasteners positioned within the support portion and/or the tissue thickness compensator which can be utilized to fasten tissue. In use, the fastener cartridge can be positioned in a first jaw of a surgical fastening device, wherein a second jaw, or anvil, can be positioned opposite the first jaw. To deploy the fasteners, a staple-deploying member is advanced through the fastener cartridge to move the fasteners toward the anvil. As the fasteners are deployed, the fasteners can capture at least a portion of the tissue thickness compensator therein along with at least a portion of the tissue being fastened.

Abstract: An anastomosis set for anastomosing a first end to be anastomosed with a second end to be anastomosed, such anastomosis set comprising: a first manipulator, with a first telescoping part at a distal end thereof, the first telescoping part is used for telescoping toward the first end to be anastomosed; a second manipulator, with a second telescoping part at a distal end thereof, the second telescoping part is used for telescoping toward the second end to be anastomosed; and an anastomosis mechanism for anastomosing the first end to be anastomosed with the second end to be anastomosed; the first manipulator including a first exit part through which the first manipulator will be removed from the first end to be anastomosed after anastomosing; the second manipulator has a second exit part, through which the second manipulator will be removed from the second end to be anastomosed after anastomosing.

Abstract: Methods and devices for increasing oxygenation levels in the blood supply and thereby treating the condition of hypoxemia. Multiple approaches such as pressure reduction in the pulmonary circulatory system, reducing triggering mechanisms in the main pulmonary artery and restricting flow in the pulmonary circulatory system are disclosed. Interventions associated with those approaches can including shunting, restrictors, compliance devices, pharmacologic substances, etc.

Abstract: A system for forming an anastomosis between first and second sections of a digestive tract includes Optical Scope Device (“OSD”) having a lumen extending therethrough and positioned at a first target site within the first section, OSD including an imagining component at a distal end thereof for viewing the first target site; First Endoscope (“FE”) including a working channel extending therethrough and positioned at a second target site within the second section; Capture Device (“CD”) extending from a proximal end to a distal end including a loop, CD extends through the lumen; First Flexible Element (“FFE”) extends through FE, FFE including a coupling element which passes through the loop to couple FFE to CD, connecting the first and second sections, the coupling element moving between insertion and locking configurations; and Stent having a lumen extending therethrough which provides fluid communication between the first and second sections.

Abstract: The present disclosure provides modular magnetic anastomosis devices that can be implemented in digestive surgery or in any circumstance of anastomosis between adjacent organs or two hollow viscera. The device is minimally invasive and easily and quickly delivered using laparoscopic or endoscopic procedures.

Abstract: A method for resetting a stapling apparatus includes providing an apparatus with a cam member in a fired position. A circuit of the apparatus is then changed from a first polarity state to a second polarity state. A motor of the apparatus is then activated to rotate the cam member from a fired position back to a home position while the circuit is in the second polarity state.

Abstract: An implantable restriction device includes a plurality of beads and a plurality of links that join the beads together. The beads include a housing including a contact surface, a passageway extending through the hosing along an axis, and at least one magnet disposed around the passageway. Portions of the links are slidably disposed in corresponding passageways of the beads such that the beads are operable to transition between a constricted configuration and an expanded configuration. The contact surfaces of adjacent beads abut against each other in the constricted configuration. Adjacent magnets within adjacent beads generate an interactive magnetic field foxed on the abutting contact surfaces of adjacent beads.

Abstract: Devices can generally include a fan portion for occluding an aneurysm neck, a channel orifice opening in the fan portion, and an agent channel for delivering a coagulating agent through the orifice into the aneurysm. Devices can be delivered through a catheter to the aneurysm, the fan portion can expand to occlude the aneurysm neck, and coagulating agent can be injected into the aneurysm. During injection of the coagulating agent, the fan portion can inhibit the coagulating agent from exiting the aneurysm. After injection of the coagulation agent, the fan portion can collapse and the device can be extracted from the patient.

Abstract: An aneurysm treatment system that includes an embolic implant, a delivery system, and an introducer sheath that are collectively designed so that the combination of the introducer sheath and the delivery system can be used as a deployment apparatus for the embolic implant. The delivery system can have a pull wire, a delivery tube, and an interference feature attached to the pull wire and positioned near a proximal end of the delivery tube. Rather than being discarded, the introducer sheath can be moved proximally over the delivery tube until it engages the interference feature. To deploy the implant, the introducer sheath can be pressed against the interference feature, causing the interference feature to move proximally in relation to the delivery tube, thereby proximally pulling the pull wire to which the interference feature is attached and deploying the implant.

Abstract: Implants can be used as flow diverters for treating aneurysms. Implants can include a stabilizing frame for anchoring the implant and an occluding element for diverting blood flow from the aneurysm neck. The stabilizing frame can have two parts, the first part sized to anchor within the sac of the aneurysm and the exterior part sized to anchor against a region of the blood vessel wall adjacent the aneurysm neck. The occluding element can be attached to the interior frame and positioned to occlude the aneurysm neck. The implant can have a central node that can be positioned near the center of the aneurysm neck at which the interior frame is attached to the exterior frame and from which the interior frame and the exterior frame extend.

Abstract: Devices, systems, and methods for treating vascular defects are disclosed herein. One aspect of the present technology, for example, includes an occlusive device comprising a mesh having a low-profile state for intravascular delivery to the aneurysm and a deployed state, the mesh comprising a first end portion, a second end portion, and a length extending between the first and second end portions, and a first lateral edge, a second lateral edge, and a width extending between the first and second lateral edges. The mesh may have a predetermined shape in the deployed state in which (a) the mesh is curved along its width, (b) the mesh is curved along its length, and (c) the mesh has an undulating contour across at least a portion of one or both of its length or its width. The mesh is configured to be positioned within the aneurysm in the deployed state such that the mesh extends over the neck of the aneurysm.