This document relates to rotational atherectomy devices and systems for removing or reducing stenotic lesions in blood vessels and/or arteriovenous grafts, for example, by rotating an abrasive element within the vessel to partially or completely remove the stenotic lesion material.
Blood flow through the peripheral arteries (e.g., iliac, femoral, renal etc.), can be affected by the development of atherosclerotic blockages. Peripheral artery disease (PAD) can be serious because without adequate blood flow, the kidneys, legs, arms, and feet may suffer irreversible damage. Left untreated, the tissue can die or harbor infection.
Patients that have kidneys that do not function properly may require hemodialysis to purify the blood of the patient. To gain access to the blood for hemodialysis, an arteriovenous fistula or a graft can be used to connect an artery and a vein. Similar to blood vessels, fistulas and/or grafts can become clogged with plaque.
This document relates to rotational atherectomy devices, systems, and methods for removing or reducing stenotic lesions in an implanted graft (e.g., a synthetic arteriovenous (AV) graft) by rotating one or more abrasive elements to abrade and breakdown the lesion. Vascular access stenosis is a common issue found in hemodialysis patients. In various embodiments, a graft can be implanted into a hemodialysis patient to access blood vessels capable of providing rapid extracorporeal blood flow during hemodialysis. The implanted graft may be prone to vascular access stenosis, which forms fibrous plaque-like lesions within the lumen of the graft and extending into the native artery and vein attached to the graft. Stenotic lesions that typically develop in association with the implanted graft can contain non-calcified neointimal hyperplasia and may lead to thrombosis and graft occlusion.
Some embodiments of the systems and devices provided herein can abrade stenotic lesions in the grafts by rotating the abrasive element(s) according to a stable and predictable orbiting profile. In some embodiments, the abrasive element(s) are attached to a distal portion of an elongate flexible drive shaft that extends from a handle assembly. In particular embodiments, a rotational atherectomy device comprises an elongate flexible drive shaft with multiple eccentric abrasive elements that are attached to the drive shaft, and one or more stability elements are attached to the drive shaft such that at least one stability element is distal of the abrasive element. Optionally, the stability elements have a center of mass that are axially aligned with a central longitudinal axis of the drive shaft while the eccentric abrasive element(s) has(have) a center(s) of mass that is(are) axially offset from central longitudinal axis of the drive shaft.
In some embodiments, multiple abrasive elements are coupled to the drive shaft and are offset from each other around the drive shaft such that the centers of the abrasive elements are disposed at differing radial angles from the drive shaft in relation to each other. For example, in some embodiments a path defined by the centers of mass of the abrasive elements defines a spiral around a length of the central longitudinal axis of the drive shaft. A flexible polymer coating may surround at least a portion of the drive shaft, including the stability element(s) in some embodiments. Also, in some optional embodiments, a distal extension portion of the drive shaft may extend distally beyond the distal-most stability element.
In one aspect, this disclosure is directed to a method for performing rotational atherectomy to remove stenotic lesion material from an arteriovenous graft of a patient. The method includes delivering a rotational atherectomy device into the arteriovenous graft. The rotational atherectomy device includes an elongate flexible drive shaft that includes a torque-transmitting coil and defines a longitudinal axis, the drive shaft being configured to rotate about the longitudinal axis, and a helical array of abrasive elements attached to a distal end portion of the drive shaft, each of the abrasive elements having a center of mass that is offset from the longitudinal axis, the centers of mass of the abrasive elements arranged along a path that spirals around the longitudinal axis. The method further includes rotating the drive shaft about the longitudinal axis such that the abrasive elements orbit around the longitudinal axis.
In another aspect, this disclosure is directed to a method for performing rotational atherectomy to remove stenotic lesion material from an arteriovenous graft of a patient. The method can include delivering a rotational atherectomy device into the arteriovenous graft. The rotational atherectomy device can include an elongate flexible drive shaft that includes a torque-transmitting coil and defines a longitudinal axis, the drive shaft being configured to rotate about the longitudinal axis, and first and second abrasive elements attached to a distal end portion of the drive shaft and each having a center of mass offset from the longitudinal axis, the center of mass of the first abrasive element being offset from the longitudinal axis at a first radial angle, the center of mass of the second abrasive element being offset from the longitudinal axis at a second radial angle that differs from the first radial angle. The method further includes rotating the drive shaft about the longitudinal axis such that the abrasive elements orbit around the longitudinal axis.
One or more of the methods can further include the embodiments described herein. In some embodiments, the method can include translationally moving the drive shaft along the longitudinal axis. The method can include modifying a speed of the drive shaft. Modifying the speed of the drive shaft can include modifying a diameter of rotation. In some embodiments, delivering the rotational atherectomy device can include delivering the rotational atherectomy device with a distal portion of the rotational atherectomy device positioned toward a vein of the patient. Delivering the rotational atherectomy device can include delivering the rotational atherectomy device with a distal portion of the rotational atherectomy device positioned toward an artery of the patient to treat a lesion at an arterial anastomosis. In some embodiments, the method can further include inflating an inflatable member on the rotational atherectomy device. In some embodiments, the rotational atherectomy device can further include a distal stability element affixed to the drive shaft and having a center of mass aligned with the longitudinal axis, the distal stability element distally spaced apart from the plurality of abrasive elements.
In yet another aspect, this disclosure is directed to a device for performing rotational atherectomy to remove stenotic lesion material from an arteriovenous graft of a patient. The device includes means for causing rotation along a longitudinal axis of the device, a first means for removing stenotic lesion material from the arteriovenous graft of the patient, the first means having a first center of mass offset from the longitudinal axis at a first radial angle, a second means for removing stenotic lesion material from the arteriovenous graft of the patient, the second means having a second center of mass offset from the longitudinal axis at a second radial angle that differs from the first radial angle, and means for mounting the means for transmitting, the first means, and the second means.
In some embodiments, the device can further include a third means for removing stenotic lesion material from the arteriovenous graft of the patient, the third means having a third center of mass offset from the longitudinal axis at a third radial angle that differs from the first radial angle and the second radial angle. In some embodiments, the second radial angle differs from the first radial angle by at least 15 degrees, and the third radial angle differs from the first radial angle and the second radial angle by at least 15 degrees. In some embodiments, a proximal-most one of the means for removing stenotic lesion material and a distal-most means for removing stenotic lesion material are each smaller than intermediate ones of the means for removing stenotic lesion material. In some embodiments, the means for stabilizing include means for removing stenotic lesion material. In some embodiments, the device further includes means for receiving a guidewire along the longitudinal axis. In some embodiments, the device also includes means for causing translational movement of the device along the longitudinal axis. In some embodiments, the device includes means for extending a distal portion of the device. In some embodiments, the device further includes means for stabilizing the means for mounting, the means for stabilizing having a center of mass aligned with the longitudinal axis.
Some of the embodiments described herein may provide one or more of the following advantages. First, some embodiments of the rotational atherectomy devices and systems operate with a stable and predictable rotary motion profile for an atherectomy procedure applied to an implanted graft (e.g., synthetic AV graft) for the removal of stenotic plaque-like lesions from within the graft. That is, when the device is being rotated in operation, the eccentric abrasive element(s) follows a predefined, consistent orbital path (offset from an axis of rotation of the device) while the stability element(s) and other portions of the device remain on or near to the axis of rotation for the drive shaft in a stable manner. This predictable orbital motion profile can be attained by the use of design features including, but not limited to, stability element(s) that have centers of mass that are coaxial with the longitudinal axis of the drive shaft, a polymeric coating on at least a portion of the drive shaft, a distal-most drive shaft extension portion, and the like. Some embodiments of the rotational atherectomy devices and systems provided herein may include one or more of such design features.
Second, the rotational atherectomy devices provided herein may include a distal stability element that has an abrasive outer surface that allows a rotational atherectomy device, when being advanced within an implanted graft, to treat plaque-like lesions that occlude or substantially occlude the graft. In such applications, the abrasive outer surface on the distal stability element may help facilitate passage of the distal stability element through plaque-like lesions that occlude or substantially occlude the graft. In some such cases, the drive shaft may be used to rotate the distal stability element to help facilitate boring of the distal stability element through such lesions in a drill-like fashion.
Third, some embodiments of the rotational atherectomy devices and systems provided herein can be used to treat various graft sizes (e.g., large-diameter grafts having an internal diameter that is multiple time greater than the outer diameter of the abrasive element) while, in some embodiments, using a small introducer sheath size for delivery of the devices and systems. In other words, in some embodiments the rotating eccentric abrasive element(s) traces an orbital path that is substantially larger than the outer diameter of the rotational atherectomy device in the non-rotating state. This feature improves the ability of the rotational atherectomy devices provided herein to treat, in some embodiments, very large grafts while still fitting within a small introducer size. In some embodiments, this feature can be at least partially attained by using a helical array of abrasive elements that has a high eccentric mass (e.g., the centers of mass of the abrasive elements are significantly offset from the central longitudinal axis of the drive shaft). Further, in some embodiments this feature can be at least partially attained by using multiple abrasive elements that are radially offset from each other around the drive shaft such that the centers of the abrasive elements are not coaxial with each other.
Fourth, in some embodiments rotational atherectomy systems described herein include user controls that are convenient and straight-forward to operate. In one such example, the user controls can include selectable elements that correspond to the diametric size of the implanted graft(s) to be treated. When the clinician-user selects the particular graft size, the system will determine an appropriate rpm of the drive shaft to obtain the desired orbit of the abrasive element(s) for the particular graft size. Hence, in such a case the clinician-user conveniently does not need to explicitly select or control the rpm of the drive shaft. In another example, the user controls can include selectable elements that correspond to the speed of drive shaft rotations. In some such examples, the user can conveniently select “low,” “medium,” or “high” speeds.
The details of one or more embodiments of the invention are set forth in the accompanying drawings and the description below. Other features, objects, and advantages of the invention will be apparent from the description and drawings, and from the claims.
Like reference symbols in the various drawings indicate like elements.
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In the depicted embodiment, the elongate flexible drive shaft assembly 130 includes a sheath 132 and a flexible drive shaft 136. A proximal end of the sheath 132 is fixed to a distal end of the handle assembly 110. The flexible drive shaft 136 is slidably and rotatably disposed within a lumen of the sheath 132. The flexible drive shaft 136 defines a longitudinal lumen in which the guidewire 134 is slidably disposed. As depicted, the flexible drive shaft 136 includes a torque-transmitting coil that defines the longitudinal lumen along a central longitudinal axis, and the drive shaft 136 is configured to rotate about the longitudinal axis while the sheath 132 remains generally stationary. Hence, as described further below, during a rotational atherectomy procedure the flexible drive shaft 136 is in motion (e.g., rotating and longitudinally translating) while the sheath 132 and the guidewire 134 are generally stationary.
The rotational atherectomy device 170 can include one or more abrasive elements 138 that are eccentrically-fixed to the drive shaft 136 proximal of a distal stability element 140. In some embodiments, the distal stability element 140 is concentrically-fixed to the drive shaft 136 between the one or more abrasive elements 138 and a distal drive shaft extension portion. As such, the center of mass of the distal stability element 140 is aligned with the central axis of the drive shaft 136 while the center of mass of each abrasive element 138 is offset from the central axis of the drive shaft 136.
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In some embodiments, the graft 32 is a self-healing graft, such that punctures in the graft caused by insertion of the rotational atherectomy device 170 will close and heal without additional aid. In some embodiments, the graft 32 can have an outer diameter of from about 4 millimeters (mm) to about 8 mm.
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In the depicted embodiment, the exposed distal end portion of the drive shaft 136 includes one or more abrasive elements 138, a (optional) distal stability element 140, and a distal drive shaft extension portion 142. In the depicted embodiment, the one or more abrasive elements 138 are eccentrically-fixed to the drive shaft 136 proximal of the distal stability element 140. In this embodiment, the distal stability element 140 is concentrically-fixed to the drive shaft 136 between the one or more abrasive elements 138 and the distal drive shaft extension portion 142. As such, the center of mass of the distal stability element 140 is aligned with the central axis of the drive shaft 136 while the center of mass of each abrasive element 138 is offset from the central axis of the drive shaft 136. The distal drive shaft extension portion 142, which includes the torque-transmitting coil, is configured to rotate about the longitudinal axis extends distally from the distal stability element 140 and terminates at a free end of the drive shaft 136.
In some optional embodiments, a proximal stability element (not shown) is included. The proximal stability element can be constructed and configured similarly to the depicted embodiment of the distal stability element 140 (e.g., a metallic cylinder directly coupled to the torque-transmitting coil of the drive shaft 136 and concentric with the longitudinal axis of the drive shaft 136) while being located proximal to the one or more abrasive elements 138.
In the depicted embodiment, the distal stability element 140 has a center of mass that is axially aligned with a central longitudinal axis of the drive shaft 136, while the one or more abrasive elements 138 (collectively and/or individually) have a center of mass that is axially offset from central longitudinal axis of the drive shaft 136. Accordingly, as the drive shaft 136 is rotated about its longitudinal axis, the principle of centrifugal force will cause the one or more abrasive elements 138 (and the portion of the drive shaft 136 to which the one or more abrasive elements 138 are affixed) to follow a transverse generally circular orbit (e.g., somewhat similar to a “jump rope” orbital movement) relative to the central axis of the drive shaft 136 (as described below, for example, in connection with
The rotating distal stability element 140 will remain generally at the longitudinal axis of the drive shaft 136 as the drive shaft 136 is rotated (as described below, for example, in connection with
The flexible drive shaft 136 of rotational atherectomy system 100 is laterally flexible so that the drive shaft 136 can readily conform to the non-linear grafts of the patient, and so that a portion of the drive shaft 136 at and adjacent to the one or more abrasive elements 138 will laterally deflect when acted on by the centrifugal forces resulting from the rotation of the one or more eccentric abrasive elements 138. In this embodiment, the drive shaft 136 comprises one or more helically wound wires (or filars) that provide one or more torque-transmitting coils of the drive shaft 136 (as described below, for example, in connection with
In this embodiment, the drive shaft 136 has a hollow core. That is, the drive shaft 136 defines a central longitudinal lumen running therethrough. The lumen can be used to slidably receive the guidewire 134 therein, as will be described further below. In some embodiments, the lumen can be used to aspirate particulate or to convey fluids that are beneficial for the atherectomy procedure.
In some embodiments, the drive shaft 136 includes an optional coating on one or more portions of the outer diameter of the drive shaft 136. The coating may also be described as a jacket, a sleeve, a covering, a casing, and the like. In some embodiments, the coating adds column strength to the drive shaft 136 to facilitate a greater ability to push the drive shaft 136 through stenotic lesions. In addition, the coating can enhance the rotational stability of the drive shaft 136 during use. In some embodiments, the coating is a flexible polymer coating that surrounds an outer diameter of the coil (but not the abrasive elements 138 or the distal stability element 140) along at least a portion of drive shaft 136 (e.g., the distal portion of the drive shaft 136 exposed outwardly from the sheath 132). In some embodiments, a portion of the drive shaft 136 or all of the drive shaft 136 is uncoated. In particular embodiments, the coating is a fluid impermeable material such that the lumen of the drive shaft 136 provides a fluid impermeable flow path along at least the coated portions of the drive shaft 136.
The coating may be made of materials including, but not limited to, PEBEX, PICOFLEX, PTFE, ePTFE, FEP, PEEK, silicone, PVC, urethane, polyethylene, polypropylene, and the like, and combinations thereof. In some embodiments, the coating covers the distal stability element 140 and the distal extension portion 142, thereby leaving only the one or more abrasive elements 138 exposed (non-coated) along the distal portion of the drive shaft 136. In alternative embodiments, the distal stability element 140 is not covered with the coating, and thus would be exposed like the abrasive elements 138. In some embodiments, two or more layers of the coating can be included on portions of the drive shaft 136. Further, in some embodiments different coating materials (e.g., with different durometers and/or stiffnesses) can be used at different locations on the drive shaft 136.
In the depicted embodiment, the distal stability element 140 is a metallic cylindrical member having an inner diameter that surrounds a portion of the outer diameter of the drive shaft 136. In some embodiments, the distal stability element 140 has a longitudinal length that is greater than a maximum exterior diameter of the distal stability element 140. In the depicted embodiment, the distal stability element 140 is coaxial with the longitudinal axis of the drive shaft 136. Therefore, the center of mass of the distal stability element 140 is axially aligned (non-eccentric) with the longitudinal axis of the drive shaft 136. In alternative rotational atherectomy device embodiments, stability element(s) that have centers of mass that are eccentric in relation to the longitudinal axis may be included in addition to, or as an alternative to, the coaxial stability elements 140. For example, in some alternative embodiments, the stability element(s) can have centers of mass that are eccentric in relation to the longitudinal axis and that are offset 180 degrees (or otherwise oriented) in relation to the center of mass of the one or more abrasive elements 138.
The distal stability element 140 may be made of a suitable biocompatible material, such as a higher-density biocompatible material. For example, in some embodiments the distal stability element 140 may be made of metallic materials such as stainless steel, tungsten, molybdenum, iridium, cobalt, cadmium, and the like, and alloys thereof. The distal stability element 140 has a fixed outer diameter. That is, the distal stability element 140 is not an expandable member in the depicted embodiment. The distal stability element 140 may be mounted to the filars of the drive shaft 136 using a biocompatible adhesive, by welding, by press fitting, and the like, and by combinations thereof. The coating may also be used in some embodiments to attach or to supplement the attachment of the distal stability element 140 to the filars of the drive shaft 136. Alternatively, the distal stability element 140 can be integrally formed as a unitary structure with the filars of the drive shaft 136 (e.g., using filars of a different size or density, using filars that are double-wound to provide multiple filar layers, or the like). The maximum outer diameter of the distal stability element 140 may be smaller than the maximum outer diameters of the one or more abrasive elements 138.
In some embodiments, the distal stability element 140 has an abrasive coating on its exterior surface. For example, in some embodiments a diamond coating (or other suitable type of abrasive coating) is disposed on the outer surface of the distal stability element 140. In some cases, such an abrasive surface on the distal stability element 140 can help facilitate the passage of the distal stability element 140 through vessel restrictions (such as calcified areas of a blood vessel).
In some embodiments, the distal stability element 140 has an exterior cylindrical surface that is smoother and different from an abrasive exterior surface of the one or more abrasive elements 138. That may be the case whether or not the distal stability element 140 have an abrasive coating on its exterior surface. In some embodiments, the abrasive coating on the exterior surface of the distal stability element 140 is rougher than the abrasive surfaces on the one or more abrasive elements 138.
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In the depicted embodiment, the two outermost abrasive elements are smaller in maximum diameter than the three inner abrasive elements. In some embodiments, all of the abrasive elements are the same size. In particular embodiments, three or more different sizes of abrasive elements are included. Any and all such possible arrangements of sizes of abrasive elements are envisioned and within the scope of this disclosure.
Also, in the depicted embodiment, the center of mass of each abrasive element 138 is offset from the longitudinal axis of the drive shaft 136. Therefore, as the eccentric one or more abrasive elements 138 are rotated (along an orbital path), at least a portion of the abrasive surface of the one or more abrasive elements 138 can make contact with surrounding stenotic lesion material. As with the distal stability element 140, the eccentric one or more abrasive elements 138 may be mounted to the filars of the torque-transmitting coil of the drive shaft 136 using a biocompatible adhesive, high temperature solder, welding, press fitting, and the like. In some embodiments, a hypotube is crimped onto the drive shaft and an abrasive element is laser welded to the hypotube. Alternatively, the one or more abrasive elements 138 can be integrally formed as a unitary structure with the filars of the drive shaft 136 (e.g., using filars that are wound in a different pattern to create an axially offset structure, or the like).
In some embodiments, the spacing of the distal stability element 140 relative to the one or more abrasive elements 138 and the length of the distal extension portion 142 can be selected to advantageously provide a stable and predictable rotary motion profile during high-speed rotation of the drive shaft 136. For example, in embodiments that include the distal drive shaft extension portion 142, the ratio of the length of the distal drive shaft extension 142 to the distance between the centers of the one or more abrasive elements 138 and the distal stability element 140 is about 1:0.5, about 1:0.8, about 1:1, about 1.1:1, about 1.2:1, about 1.5:1, about 2:1, about 2.5:1, about 3:1, or higher than 3:1.
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In the depicted embodiment, the carriage assembly includes a valve actuator. In some embodiments, an electric motor for driving rotations of the drive shaft 136 is coupled to the carriage assembly such that the valve actuator is an electrical switch instead. In the depicted embodiment, the valve actuator is a button that can be depressed to actuate a compressed gas control valve (on/off; defaulting to off) mounted to the carriage assembly. While the valve actuator is depressed, a compressed gas (e.g., air, nitrogen, etc.) is supplied through the valve to a turbine member that is rotatably coupled to the carriage assembly and fixedly coupled to the drive shaft 136. Hence, an activation of the valve actuator will result in a rotation of the turbine member and, in turn, the drive shaft 136 (as depicted by arrow 137). In some embodiments, the rotational atherectomy system 100 is configured to rotate the drive shaft 136 at a high speed of rotation (e.g., 20,000-160,000 rpm) such that the eccentric one or more abrasive elements 138 revolve in an orbital path to thereby contact and remove portions of a target lesion (even those portions of the lesion that are spaced farther from the axis of the drive shaft 136 than the maximum radius of the one or more abrasive elements 138).
To operate the handle assembly 110 during a rotational atherectomy procedure, a clinician can grasp the carriage assembly and depress the valve actuator with the same hand. The clinician can move (translate) the carriage assembly distally and proximally by hand (e.g., back and forth in relation to the housing), while maintaining the valve actuator in the depressed state. In that manner, a target lesion(s) can be ablated radially and longitudinally by virtue of the resulting orbital rotation and translation of the one or more abrasive elements 138, respectively.
During an atherectomy treatment, in some cases the guidewire 134 is left in position in relation to the drive shaft 136 generally as shown. For example, in some cases the portion of the guidewire 134 that is extending beyond the distal end of the drive shaft 136 (or extension portion 142) is about 4 inches to about 8 inches (about 10 cm to about 20 cm), about 8 inches to about 12 inches (about 20 cm to about 30 cm), about 4 inches to about 16 inches (about 10 cm to about 40 cm), or about 2 inches to about 20 inches (about 5 cm to about 50 cm). In some cases, the guidewire 134 is pulled back to be within (while not extending distally from) the drive shaft 136 during an atherectomy treatment. The distal end of the guidewire 134 may be positioned anywhere within the drive shaft 136 during an atherectomy treatment. In some cases, the guidewire 134 may be completely removed from within the drive shaft during an atherectomy treatment. The extent to which the guidewire 134 is engaged with the drive shaft 136 during an atherectomy treatment may affect the size of the orbital path of the one or more abrasive elements 138.
In the depicted embodiment, the handle assembly 110 also includes a guidewire detention mechanism 118. The guidewire detention mechanism 118 can be selectively actuated (e.g., rotated) to releasably clamp and maintain the guidewire 134 in a stationary position relative to the handle assembly 110 (and, in turn, stationary in relation to rotations of the drive shaft 136 during an atherectomy treatment). While the drive shaft 136 and handle assembly 110 are being advanced over the guidewire 134 to put the one or more abrasive elements 138 into a targeted position within a patient's graft 32, the guidewire detention mechanism 118 will be unactuated so that the handle assembly 110 is free to slide in relation to the guidewire 134. Then, when the clinician is ready to begin the atherectomy treatment, the guidewire detention mechanism 118 can be actuated to releasably detain/lock the guidewire 134 in relation to the handle assembly 110. That way the guidewire 134 will not rotate while the drive shaft 136 is rotating, and the guidewire 134 will not translate while the carriage assembly is being manually translated.
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In some embodiments, the controller 150 is pole-mounted. The controller 150 can be used to control particular operations of the handle assembly 110 and the drive shaft assembly 130. For example, the controller 150 can be used to compute, display, and adjust the rotational speed of the drive shaft 136.
In some embodiments, the controller 150 can include electronic controls that are in electrical communication with a turbine RPM sensor located on the carriage assembly. The controller 150 can convert the signal(s) from the sensor into a corresponding RPM quantity and display the RPM on the user interface. If a speed adjustment is desired, the clinician can increase or decrease the rotational speed of the drive shaft 136. In result, a flow or pressure of compressed gas supplied from the controller 150 to the handle assembly 110 (via the cable assembly 160) will be modulated. The modulation of the flow or pressure of the compressed gas will result in a corresponding modulation of the RPM of the turbine member and of the drive shaft 136.
In some embodiments, the controller 150 includes one or more interlock features that can enhance the functionality of the rotational atherectomy system 100. In one such example, if the controller 150 does not detect any electrical signal (or a proper signal) from the turbine RPM sensor, the controller 150 can discontinue the supply of compressed gas. In another example, if a pressure of a flush liquid supplied to the sheath 132 is below a threshold pressure value, the controller 150 can discontinue the supply of compressed gas.
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In some embodiments, the user interface is configured such that the user can simply select either “LOW,” “MED,” or “HIGH” speed via the selectable inputs. Based on the user's selection of either “LOW,” “MED,” or “HIGH,” the controller 150 will provide a corresponding output for rotating the drive shaft at a corresponding rotational speed. It should be understood that the user interfaces are merely exemplary and non-limiting. That is, other types of user interface controls can also be suitably used, and are envisioned within the scope of this disclosure.
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Briefly, in some implementations the following activities may occur to achieve the deployed arrangement shown in
Next, portions of the rotational atherectomy system 100 can be inserted over the guidewire 134. For example, an opening to the lumen of the drive shaft 136 at the distal free end of the drive shaft 136 (e.g., at the distal end of the optional distal drive shaft extension portion 142) can be placed onto the guidewire 134, and then the drive shaft assembly 130 and handle assembly 110 can be gradually advanced over the guidewire 134 to the position in relation to the lesion 40. In some cases, the drive shaft 136 is disposed fully within the lumen of the sheath 132 during the advancing. In some cases, a distal end portion of the drive shaft 136 extends from the distal end opening 143 of the sheath 132 during the advancing. Eventually, after enough advancing, the proximal end of the guidewire 134 will extend proximally from the handle assembly 110 (via the access port 120 defined by the handle housing).
In some cases (such as in the depicted example), the lesion 40 may be so large (i.e., so extensively occluding the vessel 10) that it is difficult or impossible to push the distal stability element 140 through the lesion 40. In some such cases, an abrasive outer surface on the distal stability element 140 can be used to help facilitate passage of the distal stability element 140 into or through the lesion 40. In some such cases, the drive shaft 136 can be rotated to further help facilitate the distal stability element 140 to bore into/through the lesion 40.
Next, as depicted by
In some implementations, prior to the ablation of the lesion 40 by the one or more abrasive elements 138, an inflatable member can be used as an angioplasty balloon to treat the lesion 40. That is, an inflatable member (on the sheath 132, for example) can be positioned within the lesion 40 and then inflated to compress the lesion 40 against the inner wall 38 of the graft 32. Thereafter, the rotational atherectomy procedure can be performed. In some implementations, such an inflatable member can be used as an angioplasty balloon after the rotational atherectomy procedure is performed. In some implementations, additionally or alternatively, a stent can be placed at lesion 40 using an inflatable member on the sheath 132 (or another balloon member associated with the drive shaft assembly 130) after the rotational atherectomy procedure is performed.
The guidewire 134 may remain extending from the distal end of the drive shaft 136 during the atherectomy procedure as shown. For example, as depicted by
To perform the atherectomy procedure, the drive shaft 136 is rotated at a high rate of rotation (e.g., 20,000-160,000 rpm) such that the eccentric one or more abrasive elements 138 revolve in an orbital path about an axis of rotation and thereby contacts and removes portions of the lesion 40.
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In some implementations, as the one or more abrasive elements 138 rotates, the clinician operator slowly advances the carriage assembly distally (and, optionally, reciprocates both distally and proximally) in a longitudinal translation direction so that the abrasive surface of the one or more abrasive elements 138 scrapes against additional portions of the occluding lesion 40 to reduce the size of the occlusion, and to thereby improve the blood flow through the graft 32. This combination of rotational and translational motion of the one or more abrasive elements 138 is depicted by the sequence of
In some embodiments, the sheath 132 may define one or more lumens (e.g., the same lumen as, or another lumen than, the lumen in which the drive shaft 136 is located) that can be used for aspiration (e.g., of abraded particles of the lesion 40). In some cases, such lumens can be additionally or alternatively used to deliver perfusion and/or therapeutic substances to the location of the lesion 40, or to prevent backflow of blood from graft 32 into sheath 132.
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In the depicted embodiment, the one or more abrasive elements 138 includes a total of five discrete abrasive elements that are spaced apart from each other. In some embodiments, one, two, three, four, five, six, seven, eight, nine, ten, eleven, twelve, thirteen, fourteen, fifteen, or more than fifteen discrete abrasive elements are included as the one or more abrasive elements 138. Each of the five discrete abrasive elements can include the abrasive media coating.
In the depicted embodiment, the two outermost abrasive elements of the abrasive elements 138 are smaller in maximum diameter than the three inner abrasive elements of the abrasive elements 138. In some embodiments, all of the abrasive elements are the same size. In particular embodiments, three or more different sizes of abrasive elements 138 are included. Any and all such possible arrangements of sizes of abrasive elements 138 are envisioned and within the scope of this disclosure.
The one or more abrasive elements 138 can be made to any suitable size. For clarity, the size of the one or more abrasive elements 138 will refer herein to the maximum outer diameter of individual abrasive elements of the one or more abrasive elements 138. In some embodiments, the one or more abrasive elements 138 are about 2 mm in size (maximum outer diameter). In some embodiments, the size of the one or more abrasive elements 138 is in a range of about 1.5 mm to about 2.5 mm, or about 1.0 mm to about 3.0 mm, or about 0.5 mm to about 4.0 mm, without limitation. Again, in a single embodiment, one or more of the abrasive elements 138 can have a different size in comparison to the other abrasive elements 138. In some embodiments, the two outermost abrasive elements are about 1.5 mm in diameter and the inner abrasive elements are about 2.0 mm in diameter.
In the depicted embodiment, the one or more abrasive elements 138, individually, are oblong in shape. A variety of different shapes can be used for the one or more abrasive elements 138. For example, in some embodiments the one or more abrasive elements 138 are individually shaped as spheres, discs, rods, cylinders, polyhedrons, cubes, prisms, and the like. In some embodiments, such as the depicted embodiment, all of the one or more abrasive elements 138 are the same shape. In particular embodiments, one or more of the abrasive elements 138 has a different shape than one or more of the other abrasive elements 138. That is, two, three, or more differing shapes of individual abrasive elements 138 can be combined on the same drive shaft 136.
In the depicted embodiment, adjacent abrasive elements of the one or more abrasive elements 138 are spaced apart from each other. For example, in the depicted embodiment the two distal-most individual abrasive elements are spaced apart from each other by a distance ‘X’. In some embodiments, the spacing between adjacent abrasive elements is consistent between all of the one or more abrasive elements 138. Alternatively, in some embodiments the spacing between some adjacent pairs of abrasive elements differs from the spacing between other adjacent pairs of abrasive elements.
In some embodiments, the spacing distance X in ratio to the maximum diameter of the abrasive elements 138 is about 1:1. That is, the spacing distance X is about equal to the maximum diameter. The spacing distance X can be selected to provide a desired degree of flexibility of the portion of the drive shaft 136 to which the one or more abrasive elements 138 are attached. In some embodiments, the ratio is about 1.5:1 (i.e., X is about 1.5 times longer than the maximum diameter). In some embodiments, the ratio is in a range of about 0.2:1 to about 0.4:1, or about 0.4:1 to about 0.6:1, or about 0.6:1 to about 0.8:1, or about 0.8:1 to about 1:1, or about 1:1 to about 1.2:1, or about 1.2:1 to about 1.4:1, or about 1.4:1 to about 1.6:1, or about 1.6:1 to about 1.8:1, or about 1.8:1 to about 2.0:1, or about 2.0:1 to about 2.2:1, or about 2.2:1 to about 2.4:1, or about 2.4:1 to about 3.0:1, or about 3.0:1 to about 4.0:1, and anywhere between or beyond those ranges.
In the depicted embodiment, the center of mass of each one of the one or more abrasive elements 138 is offset from the longitudinal axis of the drive shaft 136 along a same radial angle. Said another way, the centers of mass of all of the one or more abrasive elements 138 are coplanar with the longitudinal axis of the drive shaft 136. If the size of each of the one or more abrasive elements 138 is equal, the centers of mass of the one or more abrasive elements 138 would be collinear on a line that is parallel to the longitudinal axis of the drive shaft 136.
Referring to
It should be understood that any of the structural features described in the context of one embodiment of the rotational atherectomy devices provided herein can be combined with any of the structural features described in the context of one or more other embodiments of the rotational atherectomy devices provided herein. For example, the size and/or shape features of the one or more abrasive elements 138 can be incorporated in any desired combination with the spiral arrangement of the one or more abrasive elements 144.
Referring also to
It can be seen in
In the depicted embodiment, the radial angles of the abrasive elements 144a, 144b, 144c, 144d, and 144e differ from each other by a consistent 37.5 degrees (approximately) in comparison to the adjacent abrasive element(s). For example, the center of mass of abrasive element 144b is disposed at a radial angle B that is about 37.5 degrees different than the angle at which the center of mass of abrasive element 144a is disposed, and about 37.5 degrees different than the angle C at which the center of mass of abrasive element 144c is disposed. Similarly, the center of mass of abrasive element 144c is disposed at a radial angle C that is about 37.5 degrees different than the angle B at which the center of mass of abrasive element 144b is disposed, and about 37.5 degrees different than the angle D at which the center of mass of abrasive element 144d is disposed. The same type of relative relationships can be said about abrasive element 144d.
While the depicted embodiment has a relative radial offset of 37.5 degrees (approximately) in comparison to the adjacent abrasive element(s), a variety of other relative radial offsets are envisioned. For example, in some embodiments the relative radial offsets of the adjacent abrasive elements is in a range of about 0 degrees to about 5 degrees, or about 5 degrees to about 10 degrees, or about 10 degrees to about 15 degrees, or about 15 degrees to about 20 degrees, or about 20 degrees to about 25 degrees, or about 25 degrees to about 30 degrees, or about 30 degrees to about 35 degrees, or about 10 degrees to about 30 degrees, or about 20 degrees to about 40 degrees, or about 20 degrees to about 50 degrees.
While in the depicted embodiment, the relative radial offsets of the abrasive elements 144a, 144b, 144c, 144d, and 144e in comparison to the adjacent abrasive element(s) are consistent, in some embodiments some abrasive elements are radially offset to a greater or lesser extent than others. For example, while angles B, C, D, and E are all multiples of 37.5 degrees, in some embodiments one or more of the angles B, C, D, and/or E is not a multiple of the same angle as the others.
The direction of the spiral defined by the centers of mass of the abrasive elements 144a, 144b, 144c, 144d, and 144e can be in either direction around the drive shaft 136, and in either the same direction as the wind of the filars or in the opposing direction as the wind of the filars.
A number of embodiments of the invention have been described. Nevertheless, it will be understood that various modifications may be made without departing from the spirit and scope of the invention. For example, design features of the embodiments described herein can be combined with other design features of other embodiments described herein. Accordingly, other embodiments are within the scope of the following claims.
This application is a continuation of U.S. patent application Ser. No. 16/196,894 filed on Nov. 20, 2018, which is a continuation of U.S. patent application Ser. No. 16/008,136, filed on Jun. 14, 2018, the entire contents of which are hereby incorporated by reference.
Number | Name | Date | Kind |
---|---|---|---|
1431416 | Parsons | Oct 1922 | A |
1916085 | Summers | Jun 1933 | A |
2495316 | Clark | Jan 1950 | A |
3929129 | Archambault | Dec 1975 | A |
4445509 | Auth | May 1984 | A |
4445892 | Hussein et al. | May 1984 | A |
4620320 | Sullivan | Oct 1986 | A |
4646736 | Auth | Mar 1987 | A |
4762130 | Fogarty et al. | Aug 1988 | A |
4772258 | Marangoni et al. | Sep 1988 | A |
4784636 | Rydell | Nov 1988 | A |
4870953 | DonMicheal et al. | Oct 1989 | A |
4887469 | Shoptaw | Dec 1989 | A |
4931635 | Toyama | Jun 1990 | A |
4950238 | Sullivan | Aug 1990 | A |
4990134 | Auth | Feb 1991 | A |
5014681 | Neeman et al. | May 1991 | A |
5100425 | Fischell et al. | May 1992 | A |
5127902 | Fischell et al. | Jul 1992 | A |
5181920 | Mueller et al. | Jan 1993 | A |
5213576 | Abiuso | May 1993 | A |
5213577 | Kratzer | May 1993 | A |
5217474 | Zacca et al. | Jun 1993 | A |
5242460 | Klein et al. | Sep 1993 | A |
5250059 | Andreas et al. | Oct 1993 | A |
5250060 | Carbo et al. | Oct 1993 | A |
5273526 | Dance et al. | Dec 1993 | A |
5308354 | Zacca et al. | May 1994 | A |
5312427 | Shturman | May 1994 | A |
5314407 | Auth | May 1994 | A |
5314438 | Shturman | May 1994 | A |
5342292 | Nita et al. | Aug 1994 | A |
5361285 | Formanek | Oct 1994 | A |
5370653 | Cragg | Dec 1994 | A |
5435009 | Schild | Jul 1995 | A |
5458575 | Wang | Oct 1995 | A |
5490859 | Mische et al. | Feb 1996 | A |
5512044 | Duer | Apr 1996 | A |
5556389 | Liprie | Sep 1996 | A |
5584843 | Wulfman | Dec 1996 | A |
5649941 | Lary | Jul 1997 | A |
5681336 | Clement | Oct 1997 | A |
5730717 | Gelbfish | May 1998 | A |
5766192 | Zacca et al. | Jun 1998 | A |
5771895 | Slager | Jun 1998 | A |
5816923 | Milo | Oct 1998 | A |
5836957 | Schulz | Nov 1998 | A |
5843103 | Wulfman | Dec 1998 | A |
5868708 | Hart | Feb 1999 | A |
5893857 | Shturman | Apr 1999 | A |
6010533 | Pope | Jan 2000 | A |
6015420 | Wulfman | Jan 2000 | A |
6022363 | Walker | Feb 2000 | A |
6024749 | Shturman | Feb 2000 | A |
6030401 | Marino | Feb 2000 | A |
6066152 | Strauss | May 2000 | A |
6077282 | Shturman | Jun 2000 | A |
6096054 | Wyzgala | Aug 2000 | A |
6132444 | Shturman | Oct 2000 | A |
6135982 | Campbell | Oct 2000 | A |
6146395 | Kanz | Nov 2000 | A |
6152911 | Giannoble | Nov 2000 | A |
6156048 | Wulfman | Dec 2000 | A |
6217595 | Shturman | Apr 2001 | B1 |
6241706 | Leschinsky | Jun 2001 | B1 |
6270465 | Keith | Aug 2001 | B1 |
6416526 | Wyzgala | Jul 2002 | B1 |
6482216 | Hiblar et al. | Nov 2002 | B1 |
6485500 | Kokish | Nov 2002 | B1 |
6491660 | Guo | Dec 2002 | B2 |
6494890 | Shturman | Dec 2002 | B1 |
6497711 | Plaia | Dec 2002 | B1 |
6565588 | Clement | May 2003 | B1 |
6626861 | Hart | Sep 2003 | B1 |
6685718 | Wyzgala | Feb 2004 | B1 |
6733513 | Boyle | May 2004 | B2 |
6805485 | Hogan | Oct 2004 | B2 |
6852118 | Shturman | Feb 2005 | B2 |
6955661 | Herweck | Oct 2005 | B1 |
7252674 | Wyzgala | Aug 2007 | B2 |
7666202 | Prudnikov et al. | Feb 2010 | B2 |
7766049 | Miller | Aug 2010 | B2 |
8109954 | Shturman | Feb 2012 | B2 |
8109955 | Shturman | Feb 2012 | B2 |
8137369 | Shturman | Mar 2012 | B2 |
8142458 | Shturman | Mar 2012 | B2 |
8147507 | Shturman | Apr 2012 | B2 |
8157825 | Shturman | Apr 2012 | B2 |
8177801 | Kallok et al. | May 2012 | B2 |
8348965 | Prudnikov | Jan 2013 | B2 |
8353923 | Shturman | Jan 2013 | B2 |
8388636 | Shturman | Mar 2013 | B2 |
8388637 | Shturman | Mar 2013 | B2 |
8454638 | Shturman | Jun 2013 | B2 |
8465510 | Shturman | Jun 2013 | B2 |
8496678 | Shturman | Jul 2013 | B2 |
8500764 | Shturman | Aug 2013 | B2 |
8500765 | Shturman | Aug 2013 | B2 |
8597313 | Thatcher | Dec 2013 | B2 |
8628550 | Narveson | Jan 2014 | B2 |
8663195 | Shturman | Mar 2014 | B2 |
8663260 | Shturman | Mar 2014 | B2 |
8663261 | Shturman | Mar 2014 | B2 |
9089362 | Shturman | Jul 2015 | B2 |
8936589 | Shturman | Oct 2015 | B2 |
9192405 | Shturman | Nov 2015 | B2 |
9211138 | Shturman | Dec 2015 | B2 |
9237903 | Shturman | Jan 2016 | B2 |
9289230 | Cambronne | Mar 2016 | B2 |
9333006 | Shturman | May 2016 | B2 |
9364256 | Shturman | Jun 2016 | B2 |
9387006 | Shturman | Jul 2016 | B2 |
9597109 | Shturman | Mar 2017 | B2 |
9737329 | Shturman | Aug 2017 | B2 |
9757144 | Shturman | Sep 2017 | B2 |
9788853 | Robinson et al. | Oct 2017 | B2 |
9883886 | Shturman | Feb 2018 | B2 |
10327803 | Robinson | Jun 2019 | B2 |
10335187 | Benjamin | Jul 2019 | B2 |
10368901 | Robinson | Aug 2019 | B2 |
10441312 | Benjamin | Oct 2019 | B2 |
10463390 | Robinson | Nov 2019 | B1 |
10470794 | Robinson | Nov 2019 | B2 |
10478215 | Robinson | Nov 2019 | B2 |
10478216 | Robinson | Nov 2019 | B2 |
10478217 | Robinson | Nov 2019 | B2 |
10499946 | Robinson | Dec 2019 | B2 |
10517631 | Cambronne | Dec 2019 | B2 |
10517634 | Benjamin | Dec 2019 | B2 |
10524826 | Benjamin | Jan 2020 | B1 |
10639062 | Piippo Svendsen | May 2020 | B2 |
10639063 | Piippo Svendsen | May 2020 | B2 |
10639064 | Piippo Svendsen | May 2020 | B2 |
11147582 | Kallok | Oct 2021 | B2 |
20020007190 | Wulfman | Jan 2002 | A1 |
20020013600 | Scribner | Jan 2002 | A1 |
20020029056 | Hall | Mar 2002 | A1 |
20020082547 | Deniega | Jun 2002 | A1 |
20020099367 | Guo | Jul 2002 | A1 |
20020138088 | Nash | Sep 2002 | A1 |
20020151918 | Lafontaine | Oct 2002 | A1 |
20020188276 | Evans | Dec 2002 | A1 |
20030078606 | Lafontaine | Apr 2003 | A1 |
20030114869 | Nash | Jun 2003 | A1 |
20030125756 | Shturman | Jul 2003 | A1 |
20030139689 | Shturman | Jul 2003 | A1 |
20030199889 | Kanz | Oct 2003 | A1 |
20040098014 | Flugelman | May 2004 | A1 |
20040158270 | Wyzgala | Aug 2004 | A1 |
20050154416 | Herweck | Jul 2005 | A1 |
20050209615 | Prudnikov | Sep 2005 | A1 |
20050228402 | Hofmann | Oct 2005 | A1 |
20050240146 | Nash | Oct 2005 | A1 |
20050245864 | O'Brien | Nov 2005 | A1 |
20050256461 | DiFiore | Nov 2005 | A1 |
20060189929 | Lary | Aug 2006 | A1 |
20060258976 | Shturman et al. | Nov 2006 | A1 |
20070007190 | Pethke | Jan 2007 | A1 |
20070066888 | Maschke | Mar 2007 | A1 |
20080004643 | Schur | Jan 2008 | A1 |
20080097498 | Shimizu | Apr 2008 | A1 |
20080119946 | Nugent et al. | May 2008 | A1 |
20080161840 | Osiroff | Jul 2008 | A1 |
20080306498 | Thatcher | Dec 2008 | A1 |
20080319415 | Shturman | Dec 2008 | A1 |
20090018564 | Shturman | Jan 2009 | A1 |
20090069829 | Shturman | Mar 2009 | A1 |
20090105736 | Prudnikov | Apr 2009 | A1 |
20090182359 | Shturman | Jul 2009 | A1 |
20090264908 | Kallok | Oct 2009 | A1 |
20090312777 | Shturman | Dec 2009 | A1 |
20090318942 | Shturman | Dec 2009 | A1 |
20090326568 | Shturman | Dec 2009 | A1 |
20100010522 | Shturman | Jan 2010 | A1 |
20100049226 | Shturman | Feb 2010 | A1 |
20100211088 | Narveson | Aug 2010 | A1 |
20110009888 | Shturman | Jan 2011 | A1 |
20110054332 | Shturman | Mar 2011 | A1 |
20110213391 | Rivers et al. | Sep 2011 | A1 |
20120178986 | Campbell et al. | Jan 2012 | A1 |
20120035633 | Shturman | Feb 2012 | A1 |
20120109170 | Shturman | May 2012 | A1 |
20120150207 | Shturman | Jun 2012 | A1 |
20120172903 | Shturman | Jul 2012 | A1 |
20120191113 | Shturman | Jul 2012 | A1 |
20130178881 | Shturman | Jul 2013 | A1 |
20130204280 | Shturman | Aug 2013 | A1 |
20130245654 | Shturman | Sep 2013 | A1 |
20130274773 | Shturman | Oct 2013 | A1 |
20130296904 | Shturman | Nov 2013 | A1 |
20130296905 | Shturman | Nov 2013 | A1 |
20130310589 | Ripley | Nov 2013 | A1 |
20130310859 | Shturman | Nov 2013 | A1 |
20130333365 | Silet | Dec 2013 | A1 |
20140081298 | Cambronne | Mar 2014 | A1 |
20140180317 | Shturman | Jun 2014 | A1 |
20140180318 | Shturman | Jun 2014 | A1 |
20140180319 | Shturman | Jun 2014 | A1 |
20140296888 | Schur | Oct 2014 | A1 |
20150080795 | Mattison | Mar 2015 | A1 |
20150094733 | Shiber | Apr 2015 | A1 |
20150196320 | Robinson | Jul 2015 | A1 |
20160199093 | Cambronne et al. | Jul 2016 | A1 |
20170290603 | Svendsen et al. | Oct 2017 | A1 |
20180064464 | Robinsons et al. | Mar 2018 | A1 |
20180235652 | Benjamin | Aug 2018 | A1 |
20190083126 | Benjamin et al. | Mar 2019 | A1 |
Number | Date | Country |
---|---|---|
104955406 | Sep 2015 | CN |
20305953 | Aug 2003 | DE |
0419154 | Mar 1991 | EP |
0479433 | Apr 1992 | EP |
0820729 | Jan 1998 | EP |
1405797 | Apr 2004 | EP |
1820458 | Aug 2007 | EP |
3105978 | Dec 2016 | EP |
1595757 | Jun 1970 | FR |
854573 | Nov 1960 | GB |
2039208 | Aug 1980 | GB |
2271060 | Apr 1994 | GB |
2357573 | Jun 2001 | GB |
2426458 | Nov 2006 | GB |
WO 199714470 | Apr 1997 | WO |
WO 199850101 | Nov 1998 | WO |
WO 199944513 | Sep 1999 | WO |
WO 200115759 | Mar 2001 | WO |
WO 200209599 | Feb 2002 | WO |
WO 2003061457 | Jul 2003 | WO |
WO 2006126076 | Nov 2006 | WO |
WO 2006126175 | Nov 2006 | WO |
WO 2006126176 | Nov 2006 | WO |
WO 2008006704 | Jan 2008 | WO |
WO 2014042752 | Mar 2014 | WO |
Entry |
---|
Yevzlin, et al., “ASDIN Original Investigations: How I Do It: Directional Atherectomy for In-Stent Restenosis of a PTFE Arteriovenous Graft,” Seminars in Dialysis, 2008, 21(3):266-268. |
“Declaration of Dr. Morten Olgaard Jensen,” IPIPR2018-01658, Exhibit 1002, dated Sep. 4, 2018. |
“Declaration of Dr. Morten Olgaard Jensen,” IPR2018-01549, Exhibit 1002, dated Aug. 15, 2018. |
“Declaration of Kristina Rouw, Ph.D,” IPR2018-01549, Exhibit 2001, dated Nov. 29, 2018. |
“Declaration of Kristina Rouw, Ph.D,” IPR2018-01658, Exhibit 2001, dated Dec. 10, 2018. |
“Patent Owner's Preliminary Response,” IPR2018-01549, Paper 8, dated Nov. 29, 2018. |
“Patent Owner's Preliminary Response,” IPR2018-01658, Paper 6, dated Dec. 11, 2018. |
“Petition For Inter Partes Review of U.S. Pat. No. 9,089,362 Under 35 U.S.C. § 312 and 37 C.F.R. § 42.104,” Cardiovascular Systems, Inc. v. Cardio Flow, Inc., IPR2018-01658, Paper 1, dated Sep. 5, 2018. |
“Petition For Inter Partes Review of U.S. Pat. No. 9,788,853 Under 35 U.S.C. § 312 and 37 C.F.R. § 42.104,” Cardiovascular Systems, Inc. v. Cardio Flow, Inc., IPR2018-01549, Paper 1, dated Aug. 17, 2018. |
Declaration of Aleksey Filippov, Apr. 23, 2007, 1 page. |
Declaration of Dmitri Prudnikov, Apr. 23, 2007, 1 page. |
European Search Report in Application No. 15737946.2, dated Aug. 1, 2017, 8 pages. |
Excerpt from Deposition of Dmitri Prudnikov, Mar. 5, 2008, 7 pages. |
Excerpt from Deposition of Dmitri Prudnikov, Mar. 6, 2008, 54 pages. |
Exhibits Nos. 14, 31 & 32, from Deposition of Dmitri Prudnikov, Mar. 5, 2008, 3 pages. |
Exhibits Nos. 3 3-3 9 from Deposition of Dmitri Prudnikov, Mar. 6, 2008, 47 pages. |
Invitation To Pay Additional Fees And, Where Applicable, Protest Fee in Application No. PCT/US2017/26179, dated Jul. 6, 2017, 2 pages. |
PCT International Preliminary Report on Patentability in International Appln. No. PCT/EP2010/054548, dated Oct. 4, 2011, 8 pages. |
PCT International Preliminary Report on Patentability in International Appln. No. PCT/EP2010/054550, dated Oct. 4, 2011, 7 pages. |
PCT International Preliminary Report on Patentability, in International Application No. PCT/US2015/011212, dated Jul. 19, 2016, 8 pages. |
PCT International Search Report and Written Opinion in International Application No. PCT/US2015/011212, dated May 6, 2015. |
PCT International Search Report and Written Opinion in International Application No. PCT/US2017/26179, dated Oct. 4, 2017, 15 pages. |
PCT International Search Report and Written Opinion in International Application No. PCT/US2018/019238, dated May 8, 2018, 16 pages. |
PCT International Search Report corresponding to International Application No. PCT/EP2007/056516, dated Oct. 17, 2007, 3 pages. |
PCT International Search Report in International Application No. PCT/EP2007/062777, dated Apr. 9, 2008, 2 pages. |
PCT International Search Report in International Appln. No. PCT/EP2007/056499, dated Nov. 5, 2007, 3 pages. |
PCT International Search Report in International Appln. No. PCT/EP2007/056500, dated Dec. 11, 2007, 6 pages. |
PCT International Search Report, in International Appln. No. PCT/EP2008/065986, dated Feb. 26, 2009, 3 pages. |
Number | Date | Country | |
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20200138474 A1 | May 2020 | US |
Number | Date | Country | |
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Parent | 16196894 | Nov 2018 | US |
Child | 16733514 | US | |
Parent | 16008136 | Jun 2018 | US |
Child | 16196894 | US |