Abstract: A method of directing energy to tissue includes the initial step of positioning an energy applicator for delivery of energy to tissue. The energy applicator is operably associated with an electrosurgical power generating source. The method includes the steps of determining one or more operating parameters associated with the electrosurgical power generating source based on specific absorption rate data associated with the energy applicator, and transmitting energy from the electrosurgical power generating source through the energy applicator to tissue.

Abstract: A system for use in characterizing an energy applicator includes a test fixture assembly. The test fixture assembly includes an interior area defined therein. The system also includes a thermally-sensitive medium disposed in the interior area of the test fixture assembly. The thermally-sensitive medium includes a cut-out portion defining a void in the thermally-sensitive medium. The cut-out portion is configured to receive at least a portion of the energy applicator therein.

Abstract: An electrosurgical system includes an electrosurgical power generating source, an energy-delivery device operably associated with the electrosurgical power generating source, and a processor unit. The electrosurgical system also includes an imaging system capable of generating image data including tissue temperature information. The processor unit is disposed in operative communication with the imaging system and adapted to analyze the image data to determine a specific absorption rate around the energy-delivery device as a function of the tissue temperature information obtained from the image data.

Abstract: Methods and devices are provided for regulating a hydraulic restriction system. In general, the methods and devices can allow for non-invasive pressure control using a flow control mechanism. The flow control mechanism can be disposed between an implantable restriction device and a fluid source and include an adjustable, variably-sized fluid communication member in fluid communication with the restriction device and the fluid source. The geometry of the fluid communication member can control a rate of fluid flow between the restriction device and the fluid source, thereby also regulating a rate at which a pressure of fluid within the restriction device changes. Alternatively, the fluid flow control mechanism can include a biasing mechanism that can control the rate of fluid flow between the restriction device and the fluid source.

Abstract: A method of image analysis includes the initial step of receiving a data set including image data. The image data represents a sequence of 2-D slice images. The method includes the steps of segmenting an object of interest from surrounding image data of each slice image based on a p-value of a t-statistic relating each pixel successively examined to statistical properties derived from pixel values within the region of interest, and rendering a volume of the object of interest using (x,y) coordinates corresponding to boundaries of the segmented object of interest.

Abstract: A method of image analysis includes the initial step of receiving a data set including image data. The image data represents a sequence of 2-D slice images. The method includes the steps of segmenting an object of interest from surrounding image data of each slice image based on a topographic growth rule and a pixel intensity value threshold with respect to a starting pixel, and rendering a volume of the object of interest using (x,y) coordinates corresponding to boundaries of the segmented object of interest.

Abstract: Methods and devices are provided for deploying and applying multiple suture anchors. In one embodiment, a surgical device is provided having a shaft configured to be introduced into a body, e.g., through a scoping device, and to deliver a plurality of suture anchors, each having a suture attached thereto, into tissue, preferably without the need to remove the shaft from the body. The shaft can be configured to penetrate tissue and to deploy one or more of the suture anchors through the tissue such that the sutures extending from the deployed suture anchors extend through the tissue to allow the anchors to engage the tissue. The surgical device can also include a knotting mechanism configured to secure the sutures attached to the deployed anchors, thereby securing the anchors to the tissue.

Abstract: Devices and methods for ligating and coagulating tissue are provided. In one embodiment, a device is provided having an end effector that is adapted to access tissue to be treated at a surgical site and has the capability to both ligate and coagulate the targeted tissue. The end effector can include at least one ligation band that is removably disposed in a delivery configuration on a portion of the end effector and is adapted to be configured in a tissue-engaging configuration upon release from the end effector. The end effector can also include a pair of spaced electrodes disposed adjacent to each other on a tissue contacting portion of the end effector.

Abstract: Various exemplary methods and devices are provided for tensioning sutures. The methods and devices are particularly useful in surgical suturing applications in which it is desirable to maintain tension on a suture being delivered. In various embodiments, the device is incorporated into the handle of a suture device configured to deliver a suture to a surgical site. Other embodiments comprise a device that is separate from, but may be used in connection with, a suture device configured to deliver a suture to a surgical site. A suture locking device is also provided which enables the surgeon to ascertain when a desired amount of tension has been applied to a suture prior to affixing knotting tying elements thereto.

Abstract: Various methods and devices are provided for reorienting an implantable port. In one embodiment, an implantable port is provided and includes a base adapted to be anchored to tissue, and a housing pivotally mounted on the base and having a septum formed therein and adapted to receive fluid and to provide access to a fluid reservoir formed within the housing. In an exemplary embodiment, the housing can be pivotally mounted to the base using a ball and socket joint. For example, at least one of a distal surface of the housing and a proximal surface of the base is convex, and the other one of the distal surface of the housing and the proximal surface of the base is concave.

Abstract: An implantable restriction system having an antenna capable of being readily and predictably movable to achieve a desired orientation that is effective to communicate with an external device is provided. The antenna can be movably coupled to a housing such that the antenna can float and/or move freely with respect to the housing. The housing can be part of a gimbal element or another component of the system. The antenna can include a weight or a magnetic element to help it achieve the desired orientation. Methods for transcutaneously communicating with an implantable restriction device are also provided.

Abstract: Methods and devices are provided for regulating a hydraulic restriction system. In general, the methods and devices can allow for non-invasive pressure control using a flow control mechanism. The flow control mechanism can be disposed between an implantable restriction device and a fluid source and include an adjustable, variably-sized fluid communication member in fluid communication with the restriction device and the fluid source. The geometry of the fluid communication member can control a rate of fluid flow between the restriction device and the fluid source, thereby also regulating a rate at which a pressure of fluid within the restriction device changes. Alternatively, the fluid flow control mechanism can include a biasing mechanism that can control the rate of fluid flow between the restriction device and the fluid source.

Abstract: Methods and devices are provided for regulating a hydraulic restriction system including a restriction device. In general, the methods and devices can allow for non-invasive, transient pressure control. The methods and devices can also, in some embodiments, mechanically regulate pressure of the restriction device without using any electrical components that may need to be powered to operate over extended periods of time.

Abstract: Methods and devices are provided for regulating a restriction system. In one exemplary embodiment, a restriction system is provided having a restriction device coupled to a port with a fluid disposed therein, such that the restriction device is adapted to form a restriction in a pathway corresponding to an amount of fluid contained therein, and a pressure adjustment unit in communication with the port and effective to maintain a substantially constant equilibrium pressure between the pressure adjustment unit and the restriction device. The pressure adjustment unit is configured to regulate an amount of fluid in the restriction device in response to a fluid pressure acting thereon.

Abstract: Methods and devices are provided for regulating a restriction system. In one exemplary embodiment, a restriction system is provided having a restriction device configured to receive fluid and to form a restriction in a pathway corresponding to an amount of fluid contained therein, at least one fluid reservoir, and a fluid logic system coupled between the restriction device and the at least one fluid reservoir. The fluid logic system is configured to regulate an amount of fluid in the restriction device in response to a fluid pressure acting thereon.

Abstract: A device for loading a surgical knotting element on an applicator tool. One embodiment of the device includes a channel dimensioned to receive an applicator tool comprising a coupling. A surgical knotting element comprises a coupling complementary to the coupling of an applicator tool and a suture path. A carriage receives the surgical knotting element. The carriage is moveable in a transverse direction relative the channel between a first position where the knotting element is misaligned with the channel and a second position where the couplings are engaged with one another.

Abstract: Methods and devices are provided for performing various procedures using interchangeable end effectors. In general, the methods and devices allow a surgeon to remotely and selectively attach various interchangeable surgical end effectors to a shaft located within a patient's body, thus allowing the surgeon to perform various procedures without the need to remove the shaft from the patient's body. In an exemplary embodiment, multiple end effectors can be introduced into a body cavity. The end effectors can be disassociated or separate from one another such that they float within the body cavity. A distal end of a shaft can be positioned within the body cavity and it can be used to selectively engage one of the end effectors. In particular, the device can be configured to allow each end effector to be remotely attached and detached from the distal end of the shaft.

Abstract: A surgical fastener for fastening tissue. The fastener includes a first piece having a needle, a second piece having an opening sized for receiving the needle, and a lock for holding the needle of the first piece in the opening of the second piece. At least a portion of the first piece, the second piece and/or the lock comprises a bio-absorbable material so the fastener becomes unfastened from the tissue over time.

Abstract: Devices and methods for ligating and coagulating tissue are provided. In one embodiment, a device is provided having an end effector that is adapted to access tissue to be treated at a surgical site and has the capability to both ligate and coagulate the targeted tissue. The end effector can include at least one ligation band that is removably disposed in a delivery configuration on a portion of the end effector and is adapted to be configured in a tissue-engaging configuration upon release from the end effector. The end effector can also include a pair of spaced electrodes disposed adjacent to each other on a tissue contacting portion of the end effector.

Abstract: A medical instrument includes a shaft having a channel extending therethrough and an actuating element extending through the channel. The instrument further includes an end effector disposed on the distal end of the shaft and operatively connected to the distal end of the actuating element, wherein the actuating element is adapted to move the end effector between a first configuration and a second configuration. The instrument further includes a control moveable between a first position corresponding to the first configuration, and a second position corresponding to the second configuration, wherein the control is operatively disconnected from the actuating element when the control is in the first position.