Abstract: (EN) Respiration of a patient can be monitored by means of a device (ASD) that has the following characteristics. An inlet (IL) receives a pressurized airflow of breathable air from an airflow source. An outlet (OL) applies the pressurized airflow to a mask worn by the patient. An airflow path (AFP) is arranged between the inlet (IL) and the outlet (OL). The airflow path (AFP) has an axis (AX) and exhibits a decrease (??D) in diameter followed by an increase (+?D) in diameter in a direction from the inlet (IL) to the outlet (OL). The increase (+?D) in diameter comprises an initial portion (WI) in which the diameter increases according to a slope (?) of less than 10° with respect to the axis (AX). A pressure measurement arrangement (PS1, PS2) provides an indication (SO) of a pressure difference in the pressurized airflow between two sections (IN, T) of the airflow path that have different diameters.

Abstract: At least one embodiment is directed to an insert for measuring a parameter of the muscular-skeletal system. The insert can be temporary or permanent. In one embodiment, the insert is prosthetic component for a single compartment of the knee. The insert comprises a support structure and a support structure respectively having an articular surface and a load bearing surface. The height of the insert is less than 10 millimeters. At least one internal cavity is formed when support structures are coupled together for housing electronic circuitry, sensors, and the power source. The cavity can be sterilized through a port. A membrane is between the port and the cavity. A sterilization gas permeates the membrane for sterilizing cavity. The membrane reduces the ingress of solids and liquids to the cavity.

Abstract: In some implementations, a mobile device can be configured to monitor environmental, system and user events associated with the mobile device and/or a peer device. The occurrence of one or more events can trigger adjustments to system settings. The mobile device can be configured to keep frequently invoked applications up to date based on a forecast of predicted invocations by the user. In some implementations, the mobile device can receive push notifications associated with applications that indicate that new content is available for the applications to download. The mobile device can launch the applications associated with the push notifications in the background and download the new content. In some implementations, before running an application or communicating with a peer device, the mobile device can be configured to check energy and data budgets and environmental conditions of the mobile device and/or a peer device to ensure a high quality user experience.

Abstract: Systems and method for monitoring gait dynamics are disclosed. The performance of an orthotic or prosthetic device or other device associated with a limb may be measured based on the resistance of a bending sensor. Data from the sensors is gathered or processed, particularly for purposes of alignment, safety, failure, usage, selection, and artificial proprioception. Information relating to the device may be outputted visually or auditorily to an individual.

Abstract: An apparatus and methods for locating the axis of rotation of one or more condyles are disclosed. A condyle axis locator can include a first concave member, a second concave member, and a handle extending between the first and second concave members. The first and second concave members can include first and second locating members, respectively, extending from a surface of the first and second concave members. The first and second locating members can each include at least one opening for receiving a marking instrument. A method for locating the axis of rotation of a condyle can include positioning a first longitudinal bone in flexion relative to an adjacent second longitudinal bone, placing one of the concave members of the condyle axis locator under the condyle, and inserting a marking instrument in the opening of the locating member to mark the axis of rotation of the condyle.

Abstract: In accordance with one aspect of the present technique, a method includes receiving a plurality of images of an abdominal region from an image capture device. The method further includes identifying a bowel tissue and a peristaltic portion of the bowel tissue from the plurality of images. The method further includes determining a peristalsis property of the bowel tissue based on the peristaltic portion. The peristalsis property includes at least one of a percentage of the peristaltic portion within the bowel tissue and an amount of peristalsis in the peristaltic portion. The method also includes assessing a health the bowel tissue based on the peristalsis property of the peristaltic portion.

Abstract: The application relates to microfluidic needles and their manufacturing methods. The microfluidic needle comprises an interface portion containing at least one fluid communication channel, an elongated needle portion (40) projecting away from the interface portion (44), the needle portion having a tip and sidewalls connecting the tip to the interface portion, and at least two microfluidic channels (43 A-B) within the needle portion in fluidic connection with the at least one communication channel, the microfluidic channels being at least partly oriented parallel to the elongated needle portion. According to the application, the microfluidic channels exit the needle portion at the sidewalls of the needle portion. The needle may be fabricated by ALD-assisted silicon micromachining. The needle can be used for injection and/or sampling fluids to/from tissue or individual cells.

Abstract: In some aspects, methods of lag compensation of analyte measurements are provided. Methods of lag-compensation are provided for analyte point measurements and/or for analyte rate-of-change measurements. The methods include receiving a series of uncompensated analyte measurements and determining parameter values for analyte point and/or rate-of-change estimates based on reference analyte measurements. The analyte rate-of-change estimate is based on a sum of a plurality of scaled rates-of-changes. The analyte point estimate is based on a sum of an analyte point and a sum of a plurality of scaled rates-of-changes. Devices related to the methods are also provided.

Abstract: A method may include collecting at least one analyte from within a body, ejecting the collected at least one analyte from the body through at least one dermal layer of the body, and receiving the ejected at least one analyte outside the body. A system may include a means for collecting at least one analyte from within a body, a means for ejecting the collected at least one analyte from the body through at least one dermal layer of the body, and a means for receiving the ejected at least one analyte outside the body.

Abstract: A leg movement acquisition unit 1 continuously acquires leg movements of a sleeping subject. An apnea detection unit 2 detects whether or not the subject is in a state of apnea. A movement analysis unit 3 determines whether or not the detected leg movement satisfies previously determined conditions. These previously determined conditions include at least the following conditions (a) to (d): (a) The duration of leg movement is within a previously determined range; (b) intensity of leg movement is a previously determined value or greater; (c) leg movements satisfying conditions (a) and (b) continue for a previously determined number of times within a previously determined duration; and (d) the leg movement is not movement from immediately before to immediately after an apnea state that has been detected by the apnea detection unit. A coefficient calculation unit 4 calculates a coefficient based on the number of times of leg movement that satisfied the previously determined conditions.

Abstract: The present invention provides method for monitoring physiological status of an organ in a subject by monitoring morphological changes over time in transplanted tissue on an eye of the subject.

Abstract: An ambulatory medical device including a plurality of electrodes configured to be disposed at spaced apart positions about a patient's body, an electrode signal acquisition circuit, and a monitoring circuit. The acquisition circuit has a plurality of inputs each electrically coupled to a respective electrode of the plurality of electrodes and is configured to sense a respective signal provided by a plurality of different pairings of the plurality of electrodes. The monitoring circuit is electrically coupled to an output of the acquisition circuit and is configured to analyze the respective signal provided by each of the plurality of different pairings and to instruct the acquisition circuit to select at least one of the plurality of different pairings to monitor based on at least one of the quality of the respective signal, a phase difference between the respective signal and that of other pairings, a position of electrodes relative to the patient's body, and other criteria.

Abstract: The present invention relates to the field of ambulatory and non-invasive monitoring of a plurality of physiological parameters of a monitored individual. The invention includes a physiological monitoring apparatus with an improved monitoring apparel, the apparel having sensors for monitoring parameters reflecting pulmonary function and/or parameters reflecting cardiac function and/or parameters reflecting the function of other organ systems. The apparel is preferably also suitable for medical, athletic, and for other uses. The sensors include one or more inductive plethysmographic sensors positioned to monitor at least basic pulmonary parameters, and optionally also basic cardiac parameters. The sensors include one or more ECG sensor electrodes that preferably include a flexible, conductive fabric. The monitoring apparatus also includes an electronic unit for receiving data from the sensors and for storing the data in a computer-readable medium and/or wirelessly transmitted the data.

Abstract: A physiological monitoring system may determine a probe-off condition. A physiological sensor may be used to emit one or more wavelengths of light. A received light signal may be processed to obtain a light signal corresponding to the emitted light and an ambient signal. The signals may be analyzed to identify similar behavior. The system may determine whether the physiological sensor is properly positioned based on the analysis.

Abstract: Provided are embodiments of systems, computer medium and computer-implemented methods to monitor the health of an employee. A method for monitoring the health of an employee while the employee is located in an employee workstation including collecting, from a plurality of biometric and biomechanical sensors disposed throughout an employee workstation, health data indicative of biometric and biomechanical characteristics of the employee. The plurality of biometric and biomechanical sensors adapted to sense biometric and biomechanical characteristics of the employee and output corresponding health data indicative of the biometric and biomechanical characteristics of the employee. The method including determining an employee health profile based at least in part on the collected health data, generating a health plan for the employee based at least in part on the health profile, and displaying health content including the employee health profile and the health plan for the employee.

Abstract: A sensing device comprises a substrate material layer and a plurality of sensors provided on the substrate material layer. The plurality of sensors is electrically connected to form a loop. The loop has two output ends. There is a loop output value between the two output ends. The loop output value varies when the sensors are subjected to an external force. Each sensor has one induction value. The induction value of each sensor is different from each other. A total induction value of any one or more sensors is different from a total induction value of the other one or more sensors.

Abstract: Systems, methods, apparatuses, and software for measuring and determining physiological parameters of a patient are presented. In one example, a physiological measurement system includes a physiological sensor system configured to detect a physiological signal representative of one or more physiological parameters associated with a patient. The measurement system also includes a capacitance system configured to apply one or more electric field signals to the patient and determine a capacitance signal. The measurement system also includes a processing system configured to reduce a noise level in the physiological signal based on at least the capacitance signal.

Abstract: Methods, systems and computer-readable code for generating a forecast of a life-threatening condition, for example sepsis, in a subject, for example an infant, are disclosed. According to some embodiments, the forecast is generated in accordance with measurement values for a plurality of different vital sign parameters. In exemplary embodiments, vital sign parameters from a plurality of physiological systems are used to generate the forecast of the life-threatening condition. In exemplary embodiments, at least one vital sign parameter is other than a cardiac parameter. Non-limiting exemplary vital sign parameters may include one or more of a heart rate parameter, a respiration rate parameter, a bradycardia parameter, a desaturation parameter, a temperature parameter (for example, body temperature) and a body mass parameter.

Abstract: A gantry control panel for positioning a patient with respect to a gantry includes at least one contour of at least a portion of a figure representing a patient to be positioned with respect to a gantry, and at least one control button positioned in association with the at least one contour or as part of the at least one contour. The at least one control button controls positioning of the patient with respect to the gantry.

Abstract: An imaging stand includes: a holder configured to hold an installed cassette-type detector; a supporting member configured to support the holder from a back surface side; a circular gear secured to a shaft member protruding from a rotation center of the holder toward the supporting member on the back surface side, the holder being located in a different position from a position corresponding to the center of a radiation incidence surface of the cassette-type detector held in the holder; and a linear gear having concavities and convexities to be engaged with teeth of the circular gear, the linear gear being attached to the supporting member, wherein, when the holder holding the cassette-type detector is rotated relative to the supporting member, the rotation center of the holder linearly moves relative to the supporting member as the holder rotates, and a change is caused in orientation and position of the cassette-type detector.

Abstract: A computed-tomography (CT) apparatus that includes a CT scanner including an X-ray source, a plurality of photon-counting detectors (PCDs) arranged in a fixed detector ring to capture incident X-ray photons emitted from the X-ray source, and control circuitry configured to move at least one PCD of the plurality of PCDs, from a first position to a second position, in response to receiving an instruction to perform a scanogram scan of an object.

Abstract: A diagnostic imaging system, which can be a mobile or stationary surgical CT imaging system or an MRI system, comprises an internal airflow cooling system that includes an air intake opening and an air outtake opening that are positioned near the ground and direct air flow away from the sterile surgical field.

Abstract: An automatic selected human portion identification and adjustment device for medical treatment equipment is disclosed, in which an automatic selected human portion identification and adjustment device is included in the medical treatment equipment. The automatic selected human portion identification and adjustment device includes a depth camera, an image characteristic identification unit, and an X-ray detector position adjustment mechanism. The image characteristic identification unit performs image characteristic comparison between an instant image pixel depth signal with a predetermined image pixel depth signal for identification and generates, in response thereto, an X-ray detector position adjustment signal. Then, the X-ray detector position adjustment mechanism drives the X-ray detector to move in order to adjust the X-ray detector to correspond to the predetermined human body portion of a target human body.

Abstract: A medical image processing apparatus includes, an unit (12) extracting a blood vessel wall region from the image in a range including an aneurysm in an object, an unit (13) calculating the blood vessel diameter change rates of the neck portions of the aneurysm, blood vessel curvature, and blood vessel flattening ratio at each of discrete points on a blood vessel region based on the extracted blood vessel region, an unit (14) extracting, from discrete points, feature points at each of which at least one of a blood vessel diameter change rate, blood vessel curvature, and blood vessel flattening ratio exceeds a corresponding one of thresholds and decide a range for the indwelling of a stent graft in accordance with the extracted feature points, and a display unit (19) superimposing and display unrecommended ranges on a stored image.

Abstract: The embodiments relate to a method and device for determining plaque deposits in coronary arteries. According to the method, a coronary angiography radiography image of a subject is obtained using an imaging modality. The obtained radiography image is calibrated for further analysis of the radiography image. Image processing techniques such as thresholding and histogram equalization are applied on the radiography image to extract vessel tree structure for analysis. Further, an inner lumen width and an outer vessel width are computed based on the processed radiography image. Further, a level of plaque deposition is determined based on the inner lumen and outer vessel dimensions. Further, the result based on the analysis is displayed to the user. The result includes the level of plaque deposits within the lumen on the vascular structure and possible risks posed by the plaque deposits to a subject.

Abstract: A multiple modality imaging system includes a cone-beam computed tomography scanner which acquires CT projection data of a subject in an examination region and a nuclear imaging scanner which concurrently/subsequently acquires nuclear projection data of the subject in the examination region. A CT reconstruction processor is programmed to perform the steps of: in the CT projection data, defining a field-of-view (FoV) with a voxel grid in a trans-axial direction; determining the subject's maximum trans-axial extents; generating an extending FoV by extending the voxel grid of the FoV to at least one extended region outside the FoV that encompass at least the determined maximum trans-axial extents and all attenuation in the trans-axial direction; and iteratively reconstructing the CT projection data into an attenuation map of the extended FoV. At least one nuclear reconstruction processor is programmed to correct the acquired nuclear projection data based on the iteratively reconstructed attenuation map.

Abstract: An imaging apparatus has an AEC function that can prevent irregularities in photographed images, without being increased in size. The imaging apparatus comprises a plurality of pixels arranged in a matrix shape, each of the plurality of pixels including a conversion element for converting radiation or light into an electric charge, a plurality of lines that are connected to the plurality of pixel units and that extend in different directions to each other, a current monitor circuit that monitors currents flowing in the plurality of lines, and an arithmetic unit that calculates a two-dimensional distribution by performing back-projection processing with respect to the currents flowing in the plurality of lines monitored by the current monitor circuit.

Abstract: Upon input of a synchronization signal, which indicates a start of an X-ray emission, from a source control unit for controlling an X-ray source, an electronic cassette makes an FPD start an accumulation operation and measurement of an X-ray dose. The electronic cassette and a console command their communicators to stop communication of any signal other than a stop signal, which stops the X-ray emission from the X-ray source, during the accumulation operation of the FPD. As soon as the X-ray dose has reached a predetermined threshold value, the electronic cassette transmits the stop signal to the source control unit through the console. A delay in transmission of the stop signal due to communication congestion or signal collision does not occur, because the electronic cassette and the console stop the communication of the signal other than the stop signal.

Abstract: Systems and methods for remote diagnostic imaging. The systems include a diagnostic imaging kiosk. The kiosk includes, for example, a first housing module and a second housing module. The first housing module is configured to house, among other things, a diagnostic imaging system (e.g., an X-ray system). The second housing module is configured to house electronics associated with the operation, control, and networking of the kiosk. The electronics include, for example, a primary controller, an X-ray controller, an X-ray generator, an internal display controller, an external display controller, one or more routers, and a digital radiology module. The kiosk is configured to communicatively connect to a remote technician's workstation, and a remote technician at the workstation is able to remotely control the kiosk through a packet-switched network.

Abstract: A radiation imaging system comprises: a radiation imaging apparatus; an entry apparatus which is associated with a radiation generator; wherein the entry apparatus is configured, in response to a request received from the radiation imaging apparatus via a close proximity wireless communication connection, to send information to the radiation imaging apparatus via the close proximity wireless communication connection for connecting the radiation imaging apparatus to a wireless LAN; wherein the close proximity wireless communication connection has a communication range shorter than that of a wireless LAN; and a control unit for controlling the radiation generator and the radiation imaging apparatus, which has connected to the wireless LAN based on the information which has been sent from the entry apparatus via the close proximity wireless communication connection.

Abstract: The invention relates to a reference object (3) and a method for checking a measuring system (1), wherein a plurality of three-dimensional recordings (4, 8) of a reference object are recorded from different recording directions (5) by means of the measuring system (1). The reference object (3) has a closed shape, wherein each of the three-dimensional recordings (4) is registered with at least the preceding recording (4). In the case of a faulty calibration and/or in the case of a faulty registration, the individual recordings (4, 8) are deformed compared to the actual shape of the reference object (3), so that the deformation continues when assembling the individual three-dimensional recordings (4) to form an overall recording (54) and the generated overall recording (54) deviates in its dimensions from the dimensions of the reference object (3) as a result thereof.

Abstract: A bioacoustic sensor assembly is described including a transducer generating an acoustic signal and an actuator configured to deform a portion of the transducer to increase a signal-to-noise ratio of the acoustic signal. The disclosure also provides methods and systems for reducing the impact of noise vibrations at the transducer.

Abstract: A biological testing device includes a main unit including an ultrasonic wave transmitting/receiving part, and an attaching member for attaching the main unit on a tested object. The ultrasonic wave transmitting/receiving part includes a sensor array substrate including ultrasonic transducers, first and second resin material parts, and an ultrasonic wave transmitting medium. The first resin material part forms a first space closed off from an outside space between the first resin material part and the sensor array substrate with the first resin material part facing the ultrasonic transducers. The second resin material part forms a second space communicating with the first space. The second space is closed off from the outside space, at least a portion of the second resin material part including a flexible portion configured and arranged to bulge toward the outside space. The ultrasonic wave transmitting medium fills the first space and the second space.

Abstract: Probe includes a transducer, a PCB having a pattern part contacting the transducer via face-to-face contact, and a bonding member bonding the transducer to the pattern part of the PCB. The bonding part of the PCB is provided with the pattern part to increase a bonding area of the bonding part and to allow the bonding member to contact not only a metal layer of the bonding part but also an electrical insulation part thereof, thereby improving a bonding force between the transducer and the PCB. As a result, the transducer can be reliably bonded to the PCB, so that performance of the transducer can be prevented from being deteriorated due to defective connection between the PCB and the transducer.

Abstract: A subject information acquisition apparatus includes a first holding member that holds a subject, a probe that receives an elastic wave from the subject through the first holding member, a first holding member deformation amount measuring unit that measures an amount of deformation of the first holding member, and a processing unit that creates an area for generating subject information by using the amount of deformation of the first holding member and position information of the first holding member deformation amount measuring unit and generates an information value of subject information corresponding to the area for generating subject information by using a signal outputted by the probe.

Abstract: A device for determining the presence and/or quantity of one or more analytes in a sample of human body fluid has a container for receiving a sample of body fluid, with an interior that is delimited by a base and by a circumferential surface. It further comprises at least one test strip and a holding element for receiving and holding the one or more test strips. The holding element is designed such that it has a shape corresponding and adapted to the peripheral circumferential surface of the container. The device further comprises an elongate sampling element having an absorbent sampler that takes up the sample of body fluid and by means of which the sample of body fluid is transferred into the container. The sampling element can include an indicator strip for determining whether the amount of liquid sample sufficient for carrying out an assay.

Abstract: A biopsy device may be used to obtain and store multiple tissue samples. The device permits the tissue samples to be stored in a sequenced fashion within a generally transparent tissue storage chamber disposed at a proximal end of the biopsy device. The tissue samples can be stored on flexible tissue sample strips arranged around the circumference of a rotating vacuum manifold disposed within the chamber.

Abstract: A biopsy needle comprises a first lumen open to a tissue penetrating distal tip of the needle for receiving a tissue sample therein and a second lumen in combination with a filter separating the first and second lumens from one another, the filter being configured to permit fluids to pass therethrough while preventing the sampled tissue from passing therethrough.

Abstract: An excisional device may comprise a work element configured to rotate at a first rotation rate and comprising a first and a second articulable beak configured to cut tissue. A first helical element, configured to transport tissue cut by the first and second articulable beaks, may be co-axially disposed relative to the work element and operative to rotate at a second rotation rate that is different than the work element. A proximal sheath may be co-axially disposed relative to the work element and the first helical element, and may be configured to rotate the work element and to actuate the first and second articulable beaks.

Abstract: A biopsy device includes coaxially disposed inner and outer needles in which the outer needle tip is configured for obtaining a tissue sample. The inner surface of the outer needle includes a tissue retention feature which may include a countersink and/or a feature formed in the inner surface. The device may be introduced to a biopsy site through an introducer in which the introducer is vented and/or a certain ratio of introducer inner diameter and biopsy device outer diameter is maintained. The full core devices also permit a tighter tolerance between the I.D. and O.D. of the outer cannula and stylet, respectively, which further permits the use of a smaller gage introducer. Full devices also include a sample trap assembly operable to enlarge the sample cavity after the full core sample has been obtained.

Abstract: An elastic connector (ES) having at least two ends, each of which includes attachment means for reversibly attaching said ES to at least two components; wherein said ES is characterized by a predetermined default configuration: and, a queue-like configuration in which said ES is adapted to provide simultaneous queue-like insertion or extraction of said at least two components through a tube or endoscope's working channel or a trocar into or from a body cavity; said ES is adapted to be reversibly transformed from said predetermined default configuration to said queue-like configuration and from said queue-like configuration to said predetermined default configuration.

Abstract: Embodiments include coatings for adherence of biomaterials to a tissue. Systems and methods for adapting such coated materials to vascular access closure are further proved.

Abstract: A device for closing an aperture in a vessel wall comprising a covering member having a longitudinal axis and positionable inside the vessel against the internal opening of the aperture and having a dimension to prevent egress of fluid through the aperture and having a first opening. A first retainer is positionable external of the vessel. A flexible connecting member operatively connects the covering member and the first retainer, wherein the first opening of the covering member is configured to restrict movement of the connecting member.

Abstract: The over-the-wire interlock attachment/detachment mechanism includes a cylindrical lock receiving section of a small diameter attached to an implantable medical device such as a blood clot filter, a stent, or a septal occluder. This cylindrical lock receiving section has a plurality of spaced, curved cutouts to receive both the guide fingers and contoured locking fingers formed on a cylindrical locking section. The locking fingers are angled outwardly from the cylindrical body of the cylindrical locking section, and are moved inwardly into engagement with the curved cutouts of the cylindrical lock receiving section by a sheath which slides over the cylindrical locking section or other suitable operator.

Abstract: A surgical apparatus for positioning within a tissue tract accessing an underlying body cavity adapts to tissues having different thickness. The surgical instrument includes a proximal portion with at least one bendable structure attached thereto. The at least one bendable structure is configured to fold anywhere along its length. Folding the at least one bendable structure causes the proximal end of the proximal portion to propagate in a distal direction.

Abstract: A suture anchoring system includes a mounting sleeve having an open distal end and an open proximal end defining a passageway therethrough. The system also includes a first elongated member with an anchor suture secured thereto and a tissue suture loop. A method for securing tissue includes passing a tissue suture loop through the tissue such that opposed first and second loop sections are formed, passing an anchor suture through first and second openings respectively defined by the opposed first and second loop sections, capturing the anchor suture after passing through the first and second openings with a first elongated member attached to the anchor suture, and securing the first elongated member attached to the anchor suture to a desired anchor hole in an anatomical site.

Abstract: A prosthesis for use with a tissue repair system is capable of expanding during implantation into the tissue. The prosthesis can include a driving portion and a base portion. The driving portion helps drive the prosthesis into a tissue during a first stage of implantation. The base portion is configured to expand or splay open during a second stage of implantation. The prosthesis may include a hole for receiving a portion of a suture thread.

Abstract: A knotless suture anchoring system includes an outer anchor having a central channel and a distal tip adapted to penetrate tissue. An inner anchor is positionable in the central channel of the outer anchor and a locking feature on one or both of the inner and outer anchors retains the inner anchor within the central channel. A continuous length of suture is coupled with the inner and outer suture anchors and has a free end. At least one of the inner and the outer anchors also has a cinching mechanism that allows the suture to be tensioned by passage of the suture through the cinching mechanism in a first direction while movement of the suture through the cinching mechanism in a second direction opposite the first direction is constrained.

Abstract: Soft anchor constructs and methods for soft tissue to bone repairs. The soft anchors may be knotted or knotless constructs. The soft anchors include a body formed of various soft materials (including, but not limited to, suture) and provided in various shapes and configurations that confer the anchors the ability to be easily inserted within bone tunnels or sockets and be bunched up within the bone tunnels or sockets. At least one closed loop or soft eyelet is attached to the soft anchor to allow additional sliding strands and/or shuttle/pull devices (suture passing devices) to pass through the eyelet and aid in the knotted or knotless fixation of tissue to bone.

Abstract: An implant guidance and positioning device is provided for dynamic and rigid fixation of tissue or an implant. The device includes a handle and an elongated hook connected with the handle, which may have a lumen extending therethrough or may have a socket that can receive fasteners. The device also includes a guide channel or slot disposed in the handle. The longitudinal axis of the guide channel or slot may be generally aligned with or slightly offset from a distal end of the elongated hook or socket.