Abstract: A method for recording a scan from a series of 2D X-ray projections using a C-arm X-ray apparatus allows an analytical volume reconstruction of a disk-shaped region of interest. The C-arm X-ray apparatus has a coherent, flat focus trajectory comprising three sections on which the focus of the X-ray source is moved with recording of X-ray projection views. The X-ray source emits a cone beam in the direction of an imaging X-ray detector, such as in particular a flat panel detector FPD. In some implementations, the cone beam is configured as a fan beam with a fan angle in the plane of the focus trajectory, which contains the ROI with the virtual scan center in its center, wherein the central ray of the fan beam is located on the bisector of the fan angle, and stands vertically on the ray inlet window.

Abstract: An anti-scatter grid, a detector with such an anti-scatter grid and a radiation imaging system including such a detector with an anti-scatter grid are provided. The anti-scatter grid includes at least one grid wall. The parameters of the grid wall may be adjusted to arrive a uniform scatter-to-primary ratio. The parameters of the grid wall comprise thickness, height, shape, or position of the grid wall, or width of interspace between two grid walls. The detector includes the anti-scatter grid, at least one photosensor, and at least one scintillator. The radiation system includes a radiation generator, a radiation detector with the anti-scatter grid, and a processor.

Abstract: An X-ray apparatus capable of releasing a locked rotation of a wheel using a power supplied from an auxiliary battery of an X-ray detector when a body is discharged, and a control method thereof. The X-ray apparatus includes an X-ray detector provided with a detector battery mounted thereto and configured to detect X-rays using power supplied from the detector battery. A body includes a body battery and a detector accommodation unit, in which the X-ray detector is accommodated on the outside. A wheel in the body is rotatable by a power supplied from the body battery and a brake is configured to lock a rotation of the wheel when the body battery is incapable of supplying the power. A controller controls the brake so that a locked rotation of the wheel is released by the power supplied from the detector battery when a rotation of the wheel is locked.

Abstract: Systems and methods for providing a radiopaque shield affixed to a medical device hangar. Such systems and methods reduce radiation exposure to circulating medical staff during fluoroscopy procedures and reduce equipment clutter and cost.

Abstract: Methods and apparatus for imaging with detectors having moving heads are provided. One apparatus includes a gantry and a plurality of detector units mounted to the gantry. At least some of the plurality of detector units are movable relative to the gantry to position one or more of the detector units with respect to a subject. The detector units are movable along parallel axes with respect to each other.

Abstract: A mobile fluoroscopic imaging system having a portable radiation source capable of emitting radiation in both single and, alternatively, pulse emissions and adapted to move in all degrees of freedom; a portable detector operable to detect radiation from the radiation source, wherein the detector is adapted to move independently of the radiation source in all degrees of freedom; the radiation source and detector each comprises an alignment sensor in communication with a computer; the computer is in communication with the radiation source and the detector; the position, distance and orientation of the radiation source and the detector are established by the computer; and the computer sends an activation signal to the radiation source to indicate when radiation may be emitted. Preferably, the radiation source is prevented from emission of radiation until the detector and the radiation source have achieved predetermined alignment conditions.

Abstract: An X-ray imaging apparatus includes an X-ray source to generate and irradiate X-rays; an X-ray detector installed in at least one module of one or more modules, to detect the irradiated X-rays; an Identification (ID) resistor included in the module; a port included in the X-ray detector; and a controller to determine a module in which the X-ray detector has been installed, using the ID resistor and the port. The controller may assign a static Information Provider (IP) address to the module, and determine a module in which the X-ray detector has been installed, based on the static IP address. According to the X-ray imaging apparatuses and a control method thereof, it is possible to determine an installation location of the X-ray detector, and to use the X-ray detector in various modules without having to provide separate X-ray detectors for different locations.

Abstract: Provided is a medical image imaging apparatus that images a medical image of a breast, including a determination unit configured to determine an insertion state of the breast based on a form of the breast inserted into an imaging area for the medical image from an insertion portion.

Abstract: A computed tomography (CT) imaging system includes a CT imaging unit, a display unit and at least one processor. The CT imaging unit includes an X-ray source and a CT detector. The at least one processor is operably coupled to the imaging unit and the display unit, and is configured to: acquire at least three phases of CT imaging information via the CT imaging unit; determine timing information for imaging intensity of blood vessels represented in the CT imaging information; assign corresponding colors to the blood vessels based on the timing information; reconstruct an image using the CT imaging information from the at least three phases, wherein the blood vessels depicted in the reconstructed image are represented using the corresponding colors based on the timing information; and display the image on the display unit.

Abstract: The invention relates to peripheral equalization during a mammography X-ray examination. High contrast tissue pixel values are removed from the background estimate by finding the minimum intensity values of the pixel located in the neighbourhood, which have approximately the same distance to the skin line. Thus, high attenuating pixel values may be removed from the estimate and replaced by lower attenuating tissue pixel values. After a minimum filtration, a conventional peripheral equalization is performed. This may result in less overshoots and intensity values for higher attenuating structures in the peripheral region may become more consistent with intensity values for higher attenuating structures in the fully compressed region.

Abstract: Systems and methods are disclosed for predicting healthy lumen radius and calculating a vessel lumen narrowing score. One method of identifying a lumen diameter of a patient's vasculature includes: receiving a data set including one or more lumen segmentations of known healthy vessel segments of a plurality of individuals; extracting one or more lumen features for each of the vessel segments; receiving a lumen segmentation of a patient's vasculature; determining a section of the patient's vasculature; and determining a healthy lumen diameter of the section of the patient's vasculature using the extracted one or more features for each of the known healthy vessel segments of the plurality of individuals.

Abstract: Methods for volumetric characterisation of perivascular adipose tissue use data collected by computed tomography (CT) scanning. The volumetric characterisation of perivascular adipose tissue allows the inflammatory status of underlying blood vessels to be established by CT scanning. This is of use in the diagnosis, prognosis and treatment of coronary and vascular disease.

Abstract: Disclosed are methods and devices for estimating object scatter and/or internal scatter in a multi-level photon-counting x-ray detector, as well as x-ray tomographic imaging while correcting for object and internal scatter. The x-ray detector has at least two layers of detector diodes mounted in an edge-on geometry, e.g. designed for 1) estimating the object scatter contribution to the counts in a top layer of the at least two layers based on difference(s) in counts between the top layer and lower layer(s) under the assumption the object scatter has a slowly varying spatial distribution, and/or 2) estimating counts from reabsorption of photons that have Compton scattered inside the detector based on selectively blinding some detector elements from primary radiation by placing a highly attenuating beam stop on top of the detector elements, in lower layer(s) or in both top layer and lower layer(s), and measuring the counts in those detector elements.

Abstract: A management apparatus for managing radiation imaging receives function information about a radiation imaging apparatus and communication information about communication between the radiation imaging apparatus and a radiation generation apparatus. Based on the function information or communication information received, an operation setting unit in the management apparatus sets an operation mode of the radiation imaging apparatus; and a control unit perform control corresponding to radiation imaging based on the set operation mode.

Abstract: Disclosed is a radiation image capturing system including a portable radiation image capturing apparatus and a portable console. The portable radiation image capturing apparatus can generate image data according to irradiated radiation and transmit the generated image data by wireless communication. The portable console includes a first wireless communication unit which can receive the image data transmitted from the radiation image capturing apparatus and a second wireless communication unit which can communicate with an external apparatus or system by wireless communication. The console gives priority to one wireless communication than the other between the wireless communication through the first wireless communication unit or the wireless communication through the second wireless communication unit.

Abstract: The present disclosure relates to devices and methods for embedding a standard dose checker feature within existing CT systems by obtaining and analyzing information from the existing CT system, detecting a radiation parameter value therefrom, comparing the detected radiation parameter with a predetermined threshold, and generating an operation-signal to affect the operation of the CT system based on the comparison between the detected radiation parameter and the predetermined threshold and the state of the CT system.

Abstract: A radiation imaging system includes a radiation imaging apparatus which detects radiation transmitted through an object and obtains a radiation image, and a control apparatus which controls the radiation imaging apparatus. The radiation imaging system comprises: an abnormality information obtaining unit configured to obtain abnormality information indicating an abnormality occurring in the radiation imaging apparatus; and an examination information obtaining unit configured to obtain, from examination information stored in the control apparatus, examination information corresponding to the abnormality information.

Abstract: A system for detecting valvular malfunction includes a monitoring device and a processor. The monitoring device includes a heart sound sensor configured to detect heart sounds of the patient, and a signal processor. The processor is configured to receive a signal representative of the detected heart sounds from the signal processor, wherein the processor is configured to compare the signal to a baseline signal stored in memory. The processor may be part of the monitoring device or may be part of an external device, or both.

Abstract: A medical system and method for density assessment utilizing ultrasound. The system includes a guidewire configured and dimensioned for insertion in the vessel of the patient, a sensor positioned at the distal portion of the elongated member and a connector connecting the elongated member to an indicator, the sensor determining the density and the indicator providing an indication of the determined density.

Abstract: An intervention system employs an optical shape sensing tool (32) (e.g., a brachytherapy needle having embedded optical fiber(s) and a grid (50, 90) for guiding an insertion of the optical shape sensing tool (32) into an anatomical region relative to a grid coordinate system. The intervention system further employs a registration controller (74) for reconstructing a segment or an entirety of a shape of the optical shape sensing tool (32) relative to a needle coordinate system, and for registering the needle coordinate system to the grid coordinate system as a function of a reconstructed segment/entire shape of the optical shape sensing tool (32) relative to the grid (50, 90) (i.e., reconstruction of a segment/entire shape of the OSS needle inserted into/through the grid serving as a basis for the grid/needle coordinate system registration).

Abstract: Sold-state intravascular ultrasound (IVUS) imaging devices, systems, and methods are provided. Some embodiments of the present disclosure are particularly directed to compact and efficient circuit architectures and electrical interfaces for an ultrasound transducer array used in a solid-state IVUS system. In one embodiment, an intravascular ultrasound (IVUS) device includes: a flexible elongate member; an ultrasound scanner assembly disposed at a distal portion of the flexible elongate member, the ultrasound scanner assembly including an ultrasound transducer array; an interface coupler disposed at a proximal portion of the flexible elongate member; and a cable disposed within and extending along a length of the flexible elongate member between the ultrasound scanner assembly and the interface coupler. The cable includes four conductors electrically coupling the ultrasound scanner assembly and the interface coupler.

Abstract: Sold-state intravascular ultrasound (IVUS) imaging devices, systems, and methods are provided. Some embodiments of the present disclosure are particularly directed to compact and efficient circuit architectures and electrical interfaces for an ultrasound transducer array used in a solid-state IVUS system. In one embodiment, an intravascular ultrasound (IVUS) device includes: a flexible elongate member; an ultrasound scanner assembly disposed at a distal portion of the flexible elongate member, the ultrasound scanner assembly including an ultrasound transducer array; an interface coupler disposed at a proximal portion of the flexible elongate member; and a cable disposed within and extending along a length of the flexible elongate member between the ultrasound scanner assembly and the interface coupler. The cable includes four conductors electrically coupling the ultrasound scanner assembly and the interface coupler.

Abstract: An ultrasonic diagnostic apparatus according to an embodiment includes an ultrasonic probe and processing circuitry. The ultrasonic probe collects reflected wave data in a time series manner from a region of a subject in motion. The processing circuitry generates time-series volume data from the reflected wave data collected by the ultrasonic probe. The processing circuitry calculates at least either of volume information and motion information on a region of interest of the subject by performing processing including tracking using the volume data. The processing circuitry sets one or more feature positions that represent anatomical features in the region of interest. The processing circuitry displays an MPR image that passes through at least one of the feature positions. The processing circuitry outputs at least either of the volume information and the motion information that includes the feature positions as boundaries.

Abstract: An ultrasonic probe includes ultrasonic vibrators arranged in a circumferential direction, an acoustic matching layer disposed on the ultrasonic vibrators, and a flexion section disposed between the ultrasonic vibrators adjacent to each other in the circumferential direction, and having an electrode layer acting as an electrode of the ultrasonic vibrators adjacent to each other. Further, it is also possible to configure the ultrasonic probe in which the electrode layer is exposed in the flexion section.

Abstract: An ultrasound signal processor that selectively drives a plurality of transducer elements arrayed in an ultrasound probe and executes ultrasound transmission and reception to a subject to perform velocity analysis by a color flow mapping method includes: a transmitter configured to select a transmission transducer element array from the plurality of transducer elements and perform transmission from the transmission transducer element array; a receiver configured to generate a received signal sequence for a transducer element of a reception transducer element array; a phasing adder configured to generate an acoustic line signal; and a velocity calculator configured to generate a complex acoustic line signal and calculate an average velocity, wherein the phasing adder performs delay processing for changing a method for calculating a transmission time in which the ultrasound transmitted reaches each of the observation points in at least one of the main target area and the sub-target area.

Abstract: For alert assistance for an ultrasound scanner, computer-assisted detection is applied as the patient is scanned. The user may be notified of any detected objects so that the user gathers more information when appropriate. An automated system may be configured to return to scan any detected objects. Information is gathered as part of the work flow for that given examination of the patient based on the detection. A mechanical property of the object is derived from the extra information, resulting in further information that may be used to avoid a return visit and/or increase sensitivity in survey mode scans.

Abstract: A containment device for biological samples, which comprises: a first vessel for depositing a biological sample, a lid adapted to engage the first vessel, a hermetically-sealed chamber, adapted to contain a preservative, arranged between the lid and the first vessel, elements of generating a passage between the hermetically-sealed chamber and the first vessel for the descent of the preservative from the chamber to the first vessel; the hermetically-sealed chamber is defined by a second vessel, which is inserted into the first vessel with the filling opening directed toward the lid, and by the lid itself, closed onto the first vessel, the elements of generating a passage between the hermetically-sealed chamber and the first vessel comprise a region with a pre-fracture that is defined on the second vessel and a corresponding presser that extends from the lid and is in a position to encounter the region with a pre-fracture.

Abstract: The present disclosure relates to a vascular closure device adapted for use in closing a puncture in a blood vessel after e.g. a percutaneous interventional procedure. The disclosure also relates to a method for vascular closure using such a vascular closure device.

Abstract: An apparatus for delivery of a device into a hollow organ and a method of delivery are provided. The apparatus includes an elongated tube having proximal and distal openings and being configured for carrying the device on a distal portion thereof. The apparatus further includes a tubular cover for covering at least a portion of the device when mounted on the elongated tube, the tubular cover being radially elastic and axially non-elastic. The tubular cover is retrievable into the elongated tube through the distal opening, such that when the device is mounted on the elongated tube and covered by the tubular cover, retrieval of the tubular cover into the elongated tube uncovers the device for delivery into the hollow organ.

Abstract: Retractor blade assemblies, retractors, kits, and methods of using the same. The retractor blade assembly may include a retractor blade, a pedicle screw, and a shim that connects the pedicle screw to the retractor blade. The retractor blade may have a proximal end configured to engage a retractor body and a distal end configured to retract soft tissue. The pedicle screw may have a head portion removably connected to the distal end of the retractor blade and a shaft portion configured to engage the pedicle of a vertebra. The shim couples the pedicle screw to the retractor blade. For example, the shim may include an extension portion configured to engage the retractor blade and a connection portion configured to receive and temporarily lock the pedicle screw to the retractor blade.

Abstract: The present disclosure relates to a structure used in an ophthalmic surgical procedure. The device may be used in pupil expansion or stabilization of the iris. The device is made out of an elastic or semielastic material in a shape that is conducive to easy insertion and removal as well as being optimized for atraumatic pupil expansion.

Abstract: A tongue advancer implant (101) or removal (1601) tool for a tongue manipulation system comprising: a loading mechanism configured to enable the loading of an implant or removal assembly; a propulsion element configured to be charged; a release mechanism configured to permit the propulsion element to propel the implant or removal assembly from the implant or removal tool.

Abstract: A tongue advancer assembly (305) for a tongue manipulation system, the tongue advancer assembly (305) comprising: a core mount (703) comprising a connection rod coupling configured to couple the tongue advancer assembly to a distal end of a connection rod (303); and a tongue advancer (701) configured to be coupled to the core mount (703).

Abstract: Disclosed herein are methods and devices for securing soft tissue to a rigid material such as bone. A bone anchor is described that comprises an anchor body with expandable tines and a spreader that expands the tines into bone. Also disclosed is a bone anchor that comprises a base and a top such that suture material may be attached to apertures in the anchor top or else compressed between surfaces on the base and top to secure the suture to the anchor. Also described is an inserter that can be used to insert the bone anchor into bone and move the spreader relative to the anchor body attach suture material. Also described is an inserter that can be used to insert the bone anchor into bone and move the anchor top relative to the anchor body or anchor base to attach to or clamp suture material there between.

Abstract: Devices and methods for minimally invasive suturing are disclosed. One suturing device for minimally invasive suturing includes a proximal section a distal end, and an intermediate region therebetween. The device includes a suture head assembly having a suturing needle with a pointed end and a second end. The suturing needle is capable of rotating about an axis approximately perpendicular to a longitudinal axis of the device, wherein the pointed end of the suturing needle is positioned within the suture head assembly prior to deployment of guides that are adapted and configured to guide the needle around a circular path when advanced by a drive mechanism having a needle driver for engaging and rotating the suturing needle.

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 anvil assembly is provided. The anvil assembly includes an anvil center rod, a head assembly pivotally secured to the anvil center rod assembly from an operative position to a tilted position, and a sleeve slidably disposed about the anvil center rod. The sleeve is associated with the head assembly such that movement of the head assembly from the operative position towards the tilted position effects proximal movement of the sleeve about the anvil center rod.

Abstract: A suture clip is comprised of a length of suture material with a male clip on one side and a female clip on the other side. The male clip may contain ratchets that, when engaged with the female clip, hold it in place and allow the male clip to adjustably lit within the female clip or even through it to “tighten” the suture when the male and female clips are engaged. The suture clips are configured to be used in a suture clip applicator that contains paired and opposing needles configured to hold the male clip on one side and the female clip on the other side and to cause the engagement of male and female clips and form a continuous loop through the suture material to enable the closure of fascia or other body tissues.

Abstract: An endoscopic surgical device includes a handle assembly including a drive mechanism actuatable by a trigger; and an endoscopic assembly including a proximal end portion extending from the handle assembly; a distal end portion pivotably connected to the proximal end portion of the endoscopic assembly; and a rotatable inner actuation shaft extending from the handle assembly and into the distal end portion of the endoscopic assembly, the inner actuation shaft including a flexible portion extending across the pivot connection. The surgical device includes an end effector selectively connectable to the distal end portion of the endoscopic assembly and to a distal portion of the rotatable inner actuation shaft. The end effector includes a splined inner tube rotatably supported in an outer tube; and a plurality of surgical anchors loaded in the inner tube. A timing system allows removal of the end effector at a defined trigger position.

Abstract: A surgical instrument including a handle assembly, a first endoscopic portion, a motor, and a first end effector is disclosed. The first endoscopic portion is selectively connectable to a distal portion of the handle assembly and defines a longitudinal axis. The first endoscopic portion includes a housing adjacent its proximal portion and includes an actuation member. The motor is disposed in mechanical cooperation with the housing of the first endoscopic portion and is operatively connected to the actuation member for moving the actuation member substantially along the longitudinal axis. The first end effector is selectively connectable to a distal portion of the first endoscopic portion and is configured to perform a first stapling function.

Abstract: A surgical stapling apparatus includes a staple cartridge and an anvil member. The staple cartridge includes a plurality of surgical fasteners disposed in rows of retention slots. The staple cartridge may have an annular or linear configuration of retention slots. The tissue contacting surface of the staple cartridge may be tapered or stepped. The anvil member has a tissue contacting surface that includes a number of pockets arranged for substantially aligning with the retention slots. In addition, the tissue contacting surface of the anvil member may complement the tissue contacting surface of the staple cartridge.

Abstract: A substantially U-shaped staple has a bridge, legs, and an internally disposed compression device with a bias portion having a compression surface movably disposed between the legs and a compression resistor connected to the bridge and to the compression surface and is formed to resist movement of the compression surface towards the bridge with a force.

Abstract: Tissue fasteners carried on a tissue piercing deployment wire fasten tissue layers of a mammalian body together include a first member, a second member, and a connecting member extending between the first and second members. One of the first and second members has an elongated slot permitting fastener deployment while avoiding excessive tissue compression.

Abstract: An end effector usable with a surgical instrument includes a first jaw pivotably coupled to a second jaw. The first jaw includes staple forming depressions. A staple cartridge is releasably attachable to a channel of the second jaw. A plurality of staples is disposed in the staple cartridge. A shipping wedge is releasably attached to the staple cartridge. The shipping wedge maintains the staples in their respective retention slots and is usable to separate the staple cartridge from the channel of the second jaw.

Abstract: A surgical tool is provided comprising: a jaw assembly that includes a first and second elongated jaws each having a proximal end and a distal end, wherein the proximal end of the first jaw is mounted to be rotatable about a pivot axis between an open position and a closed position; first parallel side edges secured to the first jaw that extend parallel to a longitudinal first axis of the first jaw; second parallel side edges secured to the second jaw that extend parallel to a longitudinal second axis of second jaw; a slider beam that includes a cross-beam portion sized to slidably fit between the first parallel side edges and between the second parallel side edges, a first transverse beam configured to slidably engage surfaces of the first parallel side edges facing away from the second jaw, and a second transverse beam configured to slidably engage surfaces of the second parallel side edges facing away from the first jaw; a pulley rotatably mounted to the distal end of the first jaw; and a first slider cabl

Abstract: The invention provides a system for providing improved placement of magnetic compression devices at a desired target site so as to create anastomoses between tissues. The system includes a targeted member or medium configured to be placed within a hollow body of a patient. The hollow body may include, but is not limited to, the stomach, gallbladder, pancreas, duodenum, small intestine, large intestine, bowel, vasculature, including veins and arteries, or the like. The targeted member or medium is configured to provide a target site at desired anatomical location within the hollow body for formation of an anastomosis between a first portion of tissue of the hollow body at the target site and a second portion of tissue of the hollow body.

Abstract: The present invention relates to circular anastomosis stapler and kits comprising reinforcing buttress materials and fixation tools that are slidably installed on the anvil shaft of such staplers which provides a temporary mechanical fixation of a reinforcing buttress to the anvil surface of a circular stapler during the insertion of the anvil into the tubular tissue. When the anvil, loaded with the buttress, is in the desired location, the fixation tool is pulled back along the anvil shaft and removed. The shaft is then connected to the stapling head and the stapling is performed. The present invention also relates to methods for using the kits and devices therein.

Abstract: An assembly for restoring a gastroesophageal flap valve includes a restoration device substantially free for rotation. The assembly comprises an elongated member configured to be fed through a throat, down an adjoining esophagus and into an associated stomach. The elongated member has a distal end. The assembly further comprises a gastroesophageal flap valve restoration device carried on the distal end of the elongated member for placement in the stomach, and an invaginator carried by the elongated member. The invaginator is configured to grip the esophagus and the elongated member and invaginator are coupled for restricted relative axial movement and substantially free relative rotational movement.

Abstract: An intravascular device for treating a cerebral aneurysm, the device comprising an externally controllable expandable member, the expandable member comprising a plurality of wires that define walls of the expandable member; wherein in a relaxed state of the expandable member the walls comprise at least a first wall portion in which openings defined between the wires are small enough to prevent coils positioned within the aneurysm from exiting the aneurysm, the first wall portion comprising an axial length at least as long as a neck of the aneurysm; and at least a second wall portion in which openings defined between the wires are large enough to allow blood flow through; the second wall portion axially aligned relative to the first wall portion. In some embodiments, openings of the first wall portion are small enough to reduce radial blood flow to and/or from the aneurysm.

Abstract: Thin-film mesh for medical devices, including stent and scaffold devices, and related methods are provided. Micropatterned thin-film mesh, such as thin-film Nitinol (TFN) mesh, may be fabricated via sputter deposition on a micropatterned wafer. The thin-film mesh may include slits to be expanded into pores, and the expanded thin-film mesh used as a cover for a stent device. The stent device may include two stent modules that may be implanted at a bifurcated aneurysm such that one module passes through a medial surface of the other module. The thin-film mesh may include pores with complex, fractal, or fractal-like shapes. The thin-film mesh may be used as a scaffold for a scaffold device. The thin-film scaffold may be placed in a solution including structural protein such as fibrin, seeded with cells, and placed in the body to replace or repair tissue.