Abstract: An aneurysm intrasaccular implant is provided having one or more coated regions. The implant includes a braided mesh movable from a delivery configuration having a single-layer tubular shape sized to traverse a catheter to an implanted configuration sized to be implanted in an aneurysm sac. The braided mesh can include an anti-thrombogenic coating defining a first section along the length of the braided mesh. The braided mesh can include a cell adhesion coating defining a second section along the length of the braided mesh. In the delivery confirmation, the first section can be positioned distal to the second section within the catheter. The second section is invertible to the implanted configuration such that the second section is positioned within the aneurysm sac and the first section is positioned to occlude an aneurysm neck.

Abstract: A system to stabilize and guide the growth of the spinal column includes an elongated support member having a width and a length and a guiding connector having a bone connecting portion and a guiding portion. The bone connecting portion secures the guiding connector to a vertebrae and the guiding portion has a bearing element with a passageway adapted to receive the elongated support member. The bearing element permits relative sliding movement of the elongated support element in the passageway of the bearing element. The system may further include a bone fixation element has an elongated support member receiving channel, a locking mechanism and a bone anchoring portion. The bone anchoring portion secures the bone fixation element to bone. The locking mechanism secures the elongated support member in the channel. The guiding connector is moveable along the elongated support member to permit and control the growth of the spinal column along a predetermined path.

Abstract: Technologies for a monitoring system for monitoring a user's movement include a sensor module and a monitoring device. The sensor module is attached to the user or wearable by the user. The monitoring device detects the sensor module positioned in proximity to the monitoring device, receives sensor data from the detected sensor module, analyzes the received sensor data to determine a position and an orientation of the detected sensor module relative to the monitoring device, compares the determined positions of the detected sensor module to predefined planned positions, and initiates an alert notification in response to a determination that a difference between the determined positions of the detected sensor module and the predefined positions is greater than a reference threshold.

Abstract: The present disclosure includes a system for retrieving a blood clot in a blood vessel using a clot retrieval device having an expansile funnel that can engage with the blood clot. The present disclosure also includes a clot retrieval device having an expandable framework that can engage with the blood clot. The expansile funnel and expandable framework can expand from a collapsed delivery state to an expanded deployed state, increasing the cross-sectional area of the clot retrieval device engaging the blood clot. The increased cross-sectional area of the clot retrieval device can increase the suction force, providing effective removal of the clot from the patient.

Abstract: Technologies for determining the spatial orientation of input imagery to produce a three-dimensional model includes a device having circuitry to obtain two-dimensional images of an anatomical object (e.g., a bone of a human joint), to determine candidate values indicative of translation and rotation of the anatomical object in the two-dimensional images, and to produce, as a function of the obtained two-dimensional images and the candidate values, a candidate three-dimensional model of the anatomical object. The circuitry is also to determine a score indicative of an accuracy of the candidate three-dimensional model, to determine whether the score satisfies a threshold, and to produce, in response to a determination that the score satisfies the threshold, data indicating that the candidate three-dimensional model is an accurate representation of the anatomical object.

Abstract: Disclosed embodiments determine, at an early stage, suitability of an intraoperative image for further intraoperative surgical analysis. The determination of suitability may be made using a first angle (such as a first obturator angle) based on at least three pelvic feature points in a preoperative image, a corresponding second angle (such as a corresponding second obturator angle) based on at least three corresponding pelvic feature points in an intraoperative image, and by comparing the first angle and the corresponding second angle to determine intraoperative image suitability. The first intra-operative image is indicated as suitable for further intraoperative analysis when an absolute value of a difference between the first angle and the corresponding second angle does not exceed a threshold. When the intraoperative image is determined as unsuitable for further intraoperative analysis, an indication of a movement direction for a fluoroscopy camera used to capture the intraoperative image is provided.

Abstract: A catheter can have a textured outer body surface with protrusions and/or indentations that can reduce friction between the outer body surface and vascular anatomy or an inner lumen of another catheter in contact with the outer body surface. The catheter can include protrusions and/or indentations on an inner lumen surface that can reduce friction between the inner lumen surface and an outer body surface of another catheter within the example catheter. The protrusions can be filled with a lubricant or vasodilating drug, and the protrusions can be configured to break to release the fluid in response to forces on the protrusion during navigation through vascular anatomy and/or an inner lumen of another catheter. The catheter can include a metallic tubular reinforcing layer with openings through which the protrusions and/or indentations extend and/or protrusions and/or indentations shaped into the reinforcing layer.

Abstract: A pull wire can be retracted from a catheter by using a retraction system having an opening sized to pass through the pull wire and engage the catheter, two clamps positioned around the pull wire, a shuttle on which the clamps are mounted, and a slider having at least one contact for contacting and moving one or both clamps. To retract the pull wire, the slider can be moved proximally, the contact(s) can engage one or both clamps on the shuttle, the clamps can move so that the clamps come together and grip the pull wire, and the slider can then be moved further proximally to translate the shuttle, clamps, and pull wire proximally thereby extracting the pull wire from the catheter. The shuttle and slider can subsequently be moved distally without translating the pull wire.

Abstract: A computer-implemented method for producing a treatment plan to control manipulation of a fixation apparatus including a first element and a second ring and struts to correct an anatomical structure deformity of first and second anatomical structure segments, including: receiving, using one or more graphical user interfaces of a computing system, configuration information associated with the fixation apparatus, the configuration information comprising one or more geometric characteristics of one or more elements of the fixation apparatus and ring deformation information; receiving, by the computing system, images of the fixation apparatus and the first and the second anatomical structure segments attached thereto; determining, by the computing system, based on the configuration information and the received images, positions and orientations of the first and the second anatomical structure segments in three-dimensional space relative to the fixation apparatus; determining the hole locations of the first elemen

Abstract: An occlusive device can include a tubular braid including an open end and a pinched end. The tubular braid can define a longitudinal axis. In a predetermined shape, the tubular braid can include an outer sack and an inner sack. The open end can include a plurality of braided wires that are deflected towards the longitudinal axis in the predetermined shape.

Abstract: An embolic implantation system configured to deliver an embolic implant intravascularly to a treatment site includes an elongated delivery tube to which the embolic implant is detachably attached by a flexible loop extending through a retaining ring or opening on the embolic implant and an elongated detachment member or pull wire extending through the delivery tube and flexible loop. The pull wire has a bump near its distal end that inhibits the pull wire from moving further distally when the bump presses distally against the flexible loop and/or retaining ring. The flexible loop and retaining ring thereby serve as a distal obstruction obstructing distal movement of the bump and thereby distal movement of the pull wire into the implant.

Abstract: A method of delivering a fusion cage to an intervertebral disc space bounded by adjacent vertebral endplates, comprising the step of delivering the fusion cage into the disc space without contacting its teeth to the vertebral endplates during delivery, wherein a sheath is interposed between a cage surface and the endplates to prevent contact therebetween during delivery.

Abstract: A vascular flow diverter includes a tubular mesh framework which includes a mesh cover and an opening. The tubular mesh framework is collapsible and configured to expand from a collapsed shape to a tubular shape when the vascular flow diverter is deployed. The mesh cover conforms to the shape of the tubular mesh, is surrounded by the tubular mesh framework, and is less porous than the tubular mesh framework. The opening is located within the mesh cover. A delivery wire passes through the opening in order to guide the flow diverter into place over an aneurysm.

Abstract: Various exemplary gas spring surgical impacting tools and methods of using gas spring surgical impacting tools are provided. In general, a surgical impacting tool includes a gas spring assembly. The gas spring assembly includes a sealed chamber configured to contained compressed gas therein. The surgical impacting tool also includes a motor configured to cause compression of the gas in the sealed chamber. The compression and decompression of the gas is configured to drive movement of a surgical implement attached to the surgical impacting tool and configured to impact bone.

Abstract: An apparatus for the approximation of two bones with a first anchor having a proximal end and a distal end configured for insertion into a first hole in a first bone. A second anchor has a proximal end and a distal end configured for insertion into a second hole in a second bone. A flexible link extends between the first and second anchors limiting a spacing from the first anchor to the second anchor when in a deployed configuration. The first hole comprises a first diameter, the second hole comprises a second diameter and the first diameter is smaller than the second diameter. The second diameter is uniform across the entire length of the second hole.

Abstract: A shoulder arthroplasty kit includes a humeral head component, a combination sizer and guide device substantially identical to the humeral component but including a including a guide bore, and a guide pin configured to be inserted into the resected surface of the humerus and configured to be guided by the guide bore to a center of the resected surface of the humerus which is covered by the at least one combination sizer and guide device.

Abstract: Methods and devices for fixation of soft tissue to bone are provided. In one embodiment, a suture anchor is provided having an elongate cylindrical body with proximal and distal ends and an inner lumen extending therethrough. The elongate body can be configured so that upon partial insertion into a bone hole, it is securely anchored within the bone hole and a suture extending through the inner lumen is freely slidable. It can also configured so that, upon further insertion into the bone hole, at least a portion of the elongate body compresses to lock the suture within the inner lumen such that the suture is prevented from sliding. In another embodiment, a suture anchor is provided having arms that have an open position for receiving a suture therebetween, and a closed position in which the suture is retained but allowed to slide freely.

Abstract: Devices and methods are provided for forming a hole in bone and implanting a suture anchor in the bone hole. The devices and methods disclosed herein allow a suture coupled to tissue to be passed through a shaft that is also configured to receive a drill bit. Exemplary guide devices are provided having a shaft with a cross-sectional shape that allows the suture to be seated in a secondary region that is offset from a primary region that receives the drill bit therethrough. A drill bit can be passed through the shaft without causing any damage to the suture extending through the shaft, and subsequently an anchor can be advanced along the suture through the shaft and guided into the bone hole.

Abstract: The disclosure extends to methods, systems, and computer program products for producing an image in light deficient environments with luminance and chrominance emitted from a controlled light source.

Abstract: A bone plate includes a first through hole extending through the plate along a first longitudinal axis from a proximal surface of the plate to a bone-facing distal surface thereof which, when the plate is placed on a target portion of bone in a desired orientation, faces the bone. An outer wall of the first through hole includes three wall sections provided with projections for receiving a screw head of a bone screw. The three wall sections are straight or convex.