Atherectomy catheter drive assemblies

Information

  • Patent Grant
  • 12171407
  • Patent Number
    12,171,407
  • Date Filed
    Wednesday, December 22, 2021
    3 years ago
  • Date Issued
    Tuesday, December 24, 2024
    2 days ago
Abstract
A drive assembly for driving an imaging catheter has a rotatable fiber and a rotatable drive shaft. The drive assembly includes a fiber optic rotating junction and a motor configured to rotate the rotatable portion of the fiber optic rotating junction. In some embodiments, the drive assembly includes a sensor configured to detect a rotational position of the fiber optic rotating junction and a processor configured to obtain the detected rotational position and stop the motor only when the fiber optic rotating junction is in a predetermined rotational position. In some embodiments, the motor includes a hollow shaft through which at least a portion of the fiber optic rotating junction extends.
Description
INCORPORATION BY REFERENCE

All publications and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication or patent application was specifically and individually indicated to be incorporated by reference.


BACKGROUND

A significant body of scientific and clinical evidence supports atherectomy as a viable primary or adjunctive therapy prior to stenting for the treatment of occlusive arterial disease. Atherectomy offers a simple mechanical advantage over alternative therapies. By removing the majority of plaque mass (debulking), a larger initial lumen is created. As a result, stent deployment is greatly enhanced. Moreover, there are advantages to atherectomy related to the arterial healing response. When circumferential radial forces are applied to the vasculature, as in the case of angioplasty or stenting, the plaque mass is displaced, forcing the vessel wall to stretch dramatically. This stretch induces injury which is a known stimulus for the cellular in-growth that leads to restenosis. By removing the disease with minimal force applied to the vessel and reducing the plaque burden prior to stent placement, large gains in lumen size can be created with decreased vessel wall injury and limited elastic recoiling. These effects have been shown to generate better acute results and lower restenosis rates.


Traditional atherectomy devices have been plagued by a number of problems that have severely limited market adoption of these devices. A significant concern in adopting these devices is that they tend to require the use of large, cumbersome, and expensive drive assemblies to control the rotation and/or axial translation of the atherectomy cutter. The drive assemblies described herein may overcome some of these hurdles.


SUMMARY OF THE DISCLOSURE

Described herein are drive assemblies for catheters having a rotatable cutter and on-board imaging.


In general, in one embodiment, a drive assembly for driving an imaging catheter has a rotatable fiber and a rotatable drive shaft. The drive assembly includes a fiber optic rotating junction having a stationary portion with a stationary fiber therein and a rotatable portion with a rotatable fiber therein. The drive assembly includes a first optical connection configured to connect the stationary fiber with a light source. The drive assembly includes a motor configured to rotate the rotatable portion of the fiber optic rotating junction. The drive assembly includes a second optical connection configured to connect the rotatable portion of the fiber optic rotating junction with both the drive shaft and the rotatable fiber of the imaging catheter so as to transmit torque from the motor to the drive shaft and the rotatable fiber of the catheter and so as to transmit light from the light source to the rotatable fiber of the catheter. The drive assembly includes a sensor configured to detect a rotational position of the fiber optic rotating junction. The drive assembly includes a processor configured to obtain the detected rotational position and stop the motor only when the fiber optic rotating junction is in a predetermined rotational position.


This and other embodiments can include one or more of the following features. The sensor can be a slot sensor configured to detect a flat on the rotary optical junction. The drive assembly can further include a locking mechanism configured to lock a handle of the imaging catheter to the drive assembly. The locking mechanism can include mechanical features to physically align the handle with respect to the drive assembly. The locking mechanism can be configured such that physical alignment of the catheter handle with respect to the drive assembly can further align an optical connection of the handle with the predetermined rotational position of the fiber optic rotating junction. The stationary and rotatable fibers can be configured to transmit an optical coherence tomography signal.


In general, in one embodiment, a method of driving an imaging catheter having a rotatable fiber and a rotatable drive shaft includes connecting a stationary fiber of a stationary portion of a fiber optic rotating junction in a drive assembly with a light source; connecting a rotatable fiber of the fiber optic rotating junction with the drive shaft and the rotatable fiber of the imaging catheter; rotating the rotatable portion of a fiber optic rotating junction with a motor in the drive assembly such that both the drive shaft and the rotatable fiber of the imaging catheter rotate and such that light is transmitted from the light source to the rotatable fiber of the imaging catheter; sensing a position of the fiber optic rotating junction; and stopping the motor based upon the sensed position only when the fiber optic rotating junction is in a predetermined rotational position.


This and other embodiments can include one or more of the following features. Sensing the position can include sensing the position with a slot sensor. The method can include locking a handle of the imaging catheter into the drive assembly. The locking mechanism can include mechanical features to physically align the catheter handle with respect to the drive assembly. Locking the handle of the imaging catheter into the drive assembly using the mechanical features can align an optical connection of the handle with the predetermined rotational position of the fiber optic rotating junction. The method can further include transmitting an optical coherence tomography signal through the stationary and rotatable fibers.


In general, in one embodiment, a drive assembly for driving an imaging catheter having a rotatable fiber and a rotatable drive shaft includes a drive assembly housing. The drive assembly further includes a fiber optic rotating junction within the housing having a stationary portion with a stationary fiber therein and a rotatable portion with a rotatable fiber therein. The drive assembly includes a first optical connection through the housing configured to connect the stationary fiber with a light source. The drive assembly includes a motor within the housing configured to rotate the rotatable portion of the fiber optic rotating junction. The drive assembly includes a second optical connection through the housing configured to connect the rotatable portion of the fiber optic rotating junction with both the drive shaft and the rotatable fiber of the imaging catheter so as to transmit torque from the motor to the drive shaft and the rotatable fiber of the catheter and so as to transmit light from the light source to the rotatable fiber of the catheter. The housing is less than 75 cubic inches in volume, and the drive assembly has a total weight of less than 2 pounds.


This and other embodiments can include one or more of the following features. The volume can be less than 40 cubic inches. The volume can be less than 20 cubic inches. The drive assembly can further include a locking mechanism configured to lock a handle of the imaging catheter to the drive assembly. The stationary and rotatable fibers can be configured to transmit an optical coherence tomography signal.


In general, in one embodiment, a drive assembly for driving an imaging catheter having a rotatable fiber and a rotatable drive shaft includes a fiber optic rotating junction having a stationary portion with a stationary fiber therein and a rotatable portion with a rotatable fiber therein. The drive assembly includes a first optical connection configured to connect the stationary fiber with a light source. The drive assembly includes a motor configured to rotate the rotatable portion of the fiber optic rotating junction. The motor has a hollow shaft configured to house a portion of the fiber optic rotating junction such that the motor and the fiber optical rotating junction are coaxial. The drive assembly includes a second optical connection configured to connect the rotatable portion of the fiber optic rotating junction with both the drive shaft and the rotatable fiber of the imaging catheter so as to transmit torque from the motor to the drive shaft and the rotatable fiber of the catheter and so as to transmit light from the light source to the rotatable fiber of the catheter.


This and other embodiments can include one or more of the following features. The rotatable fiber of the fiber optic junction can be housed within the hollow shaft. The drive assembly can further include a locking mechanism that can be configured to lock a handle of the imaging catheter to the drive assembly. The stationary and rotatable fibers can be configured to transmit an optical coherence tomography signal.


In general, in one embodiment, a drive assembly for driving an imaging catheter having a rotatable fiber and a rotatable drive shaft includes a drive assembly housing. The drive assembly further includes a fiber optic rotating junction within the housing having a stationary portion with a stationary fiber therein and a rotatable portion with a rotatable fiber therein. The drive assembly includes a first optical connection through the housing configured to connect the stationary fiber with a light source. The drive assembly includes a motor in the housing configured to rotate the rotatable portion of the fiber optic rotating junction. The drive assembly includes a linear slide in the housing configured to translate the fiber optic rotating junction axially within the housing. The drive assembly includes a second optical connection through the housing configured to connect the rotatable portion of the fiber optic rotating junction with both the drive shaft and the rotatable fiber of the imaging catheter so as to transmit torque from the motor to the drive shaft and the rotatable fiber and so as to transmit light from the light source to the rotatable fiber of the catheter.


This and other embodiments can include one or more of the following features. The stationary fiber of the fiber optic rotating junction can be axially fixed at the first optical connection. The stationary fiber of the fiber optic rotating junction can include slack configured to account for translation of the fiber optic rotating junction. The drive assembly can further include a locking mechanism that can be configured to lock a handle of the imaging catheter to the drive assembly. The stationary and rotatable fibers can be configured to transmit an optical coherence tomography signal.


In general, in one embodiment, a drive assembly for driving an imaging catheter having a rotatable fiber and a rotatable drive shaft, includes a fiber optic rotating junction having a stationary portion with a stationary fiber therein and a rotatable portion with a rotatable fiber therein. The drive assembly includes a first optical connection configured to connect the stationary fiber with a light source. The drive assembly includes a motor configured to rotate the rotatable portion of the fiber optic rotating junction. The drive assembly includes a second optical connection configured to connect the rotatable portion of the fiber optic rotating junction with both the drive shaft and the rotatable fiber of the imaging catheter so as to transmit torque from the motor to the drive shaft and the rotatable fiber of the catheter and so as to transmit light from the light source to the rotatable fiber of the catheter. The drive assembly includes a magnetic locking mechanism configured to automatically align the second optical connection with the drive shaft and the rotatable fiber of the imaging catheter.


Methods of using these drive systems are also described herein.





BRIEF DESCRIPTION OF THE DRAWINGS

The novel features of the invention are set forth with particularity in the claims that follow. A better understanding of the features and advantages of the present invention will be obtained by reference to the following detailed description that sets forth illustrative embodiments, in which the principles of the invention are utilized, and the accompanying drawings of which:



FIG. 1A shows a variation of the drive assembly configured to drive an imaging catheter with a rotary cutter. The drive assembly includes a motor to drive the catheter cutter and a linear slide assembly to translate an optical assembly with a drive shaft. FIG. 1B shows the drive assembly with the outer housing removed to exhibit the interior components.



FIG. 2 A shows a handle lock of the drive assembly of FIGS. 1A and 1B. FIG. 2B shows an exploded view of the drive assembly of FIG. 2A.



FIG. 3A shows the interaction between the handle lock of FIG. 2A and a catheter handle. FIG. 3B shows the handle lock of FIG. 2A in an open position. FIG. 3C shows the handle lock of FIG. 2A in a closed position.



FIGS. 4A and 4B show the rotary optical drive subassembly of the drive assembly of FIGS. 1A and 1B.



FIG. 5A shows activation of the linear slide of the rotary optical drive subassembly of FIGS. 4A and 4B in a tissue packing position. FIG. 5B shows activation of the linear slide of the rotary optical drive subassembly of FIGS. 4A and 4B in a tissue cut position.



FIG. 6 shows the outer housing of another exemplary drive assembly.



FIGS. 7 and 8 show the drive assembly of FIG. 6 with the housing removed to show the inner components and subassemblies.



FIGS. 9A and 9B show a close-up of the distal portion of the drive assembly shown in FIGS. 7 and 8, including the locking mechanism to connect a handle to the drive assembly of FIG. 6.



FIG. 10 is a top view of the locking mechanism of FIGS. 7 and 8.



FIGS. 11A and 11B show front and side view of the locking mechanism of FIGS. 7 and 8.



FIGS. 12 and 13 show the drive assembly of FIGS. 7 and 8, including an exemplary rotary optical drive assembly.



FIGS. 14A and 14B show a close-up of an optical sensor configured to align a drive assembly (such as the drive assembly of FIGS. 7 and 8) with a catheter or catheter handle.



FIG. 15 shows an axial view of a handle lock of the drive assembly of FIGS. 7 and 8 with the optical connector aligned in top-dead-center position.



FIG. 16 shows a magnetic connector for connecting a catheter to a drive assembly.



FIG. 17 shows another exemplary drive assembly.



FIGS. 18A-18C show the drive assembly of FIG. 17 with the housing removed.



FIG. 19 is a cross-sectional diagrammatic view of the rotary optical drive subassembly of FIGS. 18A-18C.





DETAILED DESCRIPTION

Described herein are reusable drive assemblies configured to be attached to an imaging catheter, such as an atherectomy catheter. In general, the drive assemblies can include a motor to rotate both a drive shaft of the catheter and a rotating fiber of the catheter. The drive assemblies herein can further include an optical pass-through to transfer light from a light source to the rotating fiber of the catheter, such as for optical coherence tomography (OCT) imaging. The optical pass-through can include a fiber optic rotating junction having a stationary portion with a stationary fiber therein and a rotatable portion with a rotatable fiber therein. The drive assembles can be configured to attach at the proximal end to a light source and at the distal end to a catheter.


In some embodiments, a drive assembly can be configured to provide rotation of a drive shaft, simultaneous rotation of an optical fiber, translation of the drive shaft, and simultaneous translation of the fiber. Such drive assemblies could be used, for example, with a catheter having an imaging sensor and a cutter that are driven by the same drive shaft where the drive shaft can be translated proximally or distally to pack tissue and/or expose the cutter.


For example, referring to FIGS. 1A-5B, a drive assembly 100 can be configured to provide rotation of a drive shaft, rotation of an optical fiber, translation of the drive shaft, and translation of the fiber of an imaging catheter.


As shown in FIGS. 1A-1B, the drive assembly 100 can include a housing 101 (having an access door 107 therein) and a handle lock 103, to connect the drive assembly 100 to a catheter handle. As shown in FIG. 1B, the drive assembly 100 can further include a rotary optical drive subassembly 102 configured to provide rotation to the drive shaft and optical fiber of a catheter and a linear slide subassembly 104 configured to provide translation of the drive shaft and optical fiber of the catheter used with the drive assembly 100. The drive assembly 100 can be connected at a proximal end to the light source. A power source can connected to the drive assembly 100 to provide the driving power. A power button 109 can be used to turn the power to turn the drive assembly 100 on and off.


The handle lock 103 can provide a mechanical interface to secure the catheter handle to the drive assembly 100 during use. In one embodiment, as shown in FIG. 2B, the handle lock 103 can include a core 220, two retaining arms 224, and a release button 228 (the release button is also shown in FIG. 1A). The handle lock core 220 can include mating features 229 thereon configured such that the core 220 can mate with the proximal end of the catheter handle and enclose the proximal end of the catheter handle and limit radial handle movement. Axial movement of the catheter handle can be limited by the retaining arms 224 once the handle is fully seated in the lock 103.


Referring to FIG. 3A, to engage the retaining arms 224, the handle of the catheter can be inserted into the handle lock 103 such that features of the handle (such as mating wings) fit within the mating keyways 229 of the core 220, thereby allowing for self-alignment of the handle with the drive assembly 100. Once inserted, the handle can push the retaining arms 224 into the open position, as shown in FIG. 3B. After the mating features of the handle, such as wings, pass fully through the retaining arms 224, an extension spring 227 in the handle lock 103 can cause the retaining arms 224 to return to a closed position (see FIG. 3C), preventing the catheter and catheter handle from moving axially and rotationally within the sled. After use, the catheter or catheter handle can be removed from the drive assembly 100 by pushing down on the handle release button 228, which can cause the retaining arms 224 to rotate into the open position, thereby allowing the catheter handle to be removed from the handle lock 103.


Referring to FIG. 4A, the rotary optical drive subassembly 102 of the drive assembly 100 can include a fiber optic rotating junction (FORJ) 442, a motor 444, an optical connector 446, which can be connected to the drive shaft (and optical fiber) of the catheter, and an optical connector 447, which can connected to the light source. The FORJ 442 can advantageously serve to provide an optical link between light from a light source and the optical fiber of the catheter. The FORJ 442 can further advantageously serve to decouple the catheter fiber rotation from light source fiber rotation, i.e., can provide a junction for the catheter's rotating optical fiber and a static optical fiber from the light source. In one embodiment, the motor 444 can be a DC brushless motor with integrated speed controller. In use, the motor 444 can be configured to drive the FORJ through a belt-pulley system. In turn, the FORJ 442 can be configured to drive the rotation of the drive shaft and optical fiber of the catheter through the optical connector 446, which can connect directly to the drive shaft.


Thus, referring to FIG. 4B, the motor 444 and the FORJ 442 can have pulleys 445, 443, respectively, that can be connected by a belt (not shown). As the motor 444 turns (shown by arrow B), the FORJ 442 turns (shown by arrow C). The FORJ 442 can be rigidly connected to the distal optical connector 446 through mechanical couplings. Therefore, as the FORJ 442 turns, the optical connector 446 turns. When the catheter handle is attached, the distal optical connector is mechanically locked to the catheter optical connector, which is connected to the drive shaft and optical fiber of the catheter. Therefore, as the distal optical connector 446 rotates, so does the catheter drive shaft and optical fiber.


Referring to FIGS. 5A and 5B, the linear slide subassembly 104 includes a linear slide 552 having a stationary portion 554 connected to the housing 101 of the drive assembly 100 and a translatable portion 556 movable relative to the housing 101 of the drive assembly. The rotary optical drive subassembly 102 can rest on, and be fixedly attached to, the translatable portion 556 of the linear slide 552. As a result, the rotary optical drive subassembly 102 can slide axially (proximally and distally) relative to the stationary portion 554 of the linear slide 552 (and thus relative to the housing 101), as shown by the arrow A in FIG. 5A. The linear slide assembly can thus translate axially in concert with axial movement of the catheter's drive shaft and optical fiber (such as for exposing the cutter or packing the nosecone). Thus, as shown in FIGS. 5A and B, if the drive shaft and thus the cutter need to be moved distally (FIG. 5A) and/or proximally (FIG. 5B), such as to activate the nosecone or cutter deflection and/or pack tissue into the nosecone, the rotary optical subassembly 102 can move simultaneously, thereby maintaining the optical connection between the catheter and the light source.


The linear slide can include a space for slack in the optical fiber therein. For example, slack in the optical fiber can coil around within the inner perimeter of the housing 101. The slack in the optical fiber can ensure that movement of the rotary optical subassembly 102 distally will not pull the optical fiber out of the optical connection 447 with the light source (as the optical fiber can be axially fixed at the optical connection 447).


In some embodiments, movement of the rotary optical subassembly 102 can be activated through the optical connection 446 via an activation mechanism on the handle or the catheter. Thus, the rotary optical subassembly 102 can be passively moved as the parts of the catheter or handle are actively moved. A release lever 145 can be configured to either allow or restrict the rotary optical subassembly 102 from translating (thereby providing a locking mechanism to hold the rotary optical subassembly 102 in place when desired).


The axial translation of the rotary optical drive assembly 104 and the drive shaft can occur relative to the sled housing 101 and the catheter outer shaft and handle (connected to the housing 101), all of which can remain stationary. Maintaining a stationary outer shaft ensures that the outer shaft can remain axially and rotationally stabilized in the vessel while the cutter deflection and/or tissue packing occur, thereby ensuring that the physician does not lose the desired catheter position relative to the vessel.


The drive assembly 100 can advantageously provide a therapeutic amount of torque to the drive shaft/cutter of a catheter while also providing the required speed of rotation for imaging, such as OCT imaging. For example, the drive assembly 100 can provide 0.5 to 15 ounce inches of torque, such as 0.5 to 10 ounce inches, such as 1 to 5 ounce inches, such as approximately 2 ounce inches of torque.


In some embodiments, a drive assembly can be configured to provide only rotation of a drive shaft and simultaneous rotation of an optical fiber (and not translation of either). Such drive assemblies could be used, for example, with: (1) a catheter having an imaging sensor and a cutter that are driven by the same drive shaft where the drive shaft can be translated proximally or distally to pack tissue and/or expose the cutter (and where the translation mechanism is provided in the handle); or (2) a catheter having a separately rotatable imaging and cutting shaft.


For example, the drive assembly 100 described above can be used without the linear drive subassembly 102 to provide only rotation. Another drive assembly 1400 is shown with respect to FIGS. 6-15 that can be configured to provide rotation of a drive shaft and rotation of an optical fiber of an imaging catheter.


Referring to FIGS. 6-8, the drive assembly 1400 can include a housing 1402 having a rotary optical subassembly 1411, a control board (not shown), and a position sensor 1433 therein. The drive assembly 1400 can further include a connection 1401 to a cable 1403 extending to the light source as well as a handle lock 1405 to connect to a catheter handle. A power button 1407 on the housing 1402 can be used to toggle power to the drive assembly 1400.


Referring to FIGS. 9A-11B, the handle lock 1405 can be a mechanical interface which secures a catheter handle of an imaging catheter to the drive assembly 1400 during use. The handle lock 1405 can include a core 1407 to limit radial handle movement by encircling the proximal end of the catheter handle. The core 1407 can be held in place in the drive assembly 1400 by mating features 1409 at the top and bottom of the housing 1402. The catheter handle can be locked in its axial position by a handle lock bar 1411 that is loaded with a spring 1413. To lock the handle into the drive assembly 100, mating feature (such as a wing) on the handle is aligned with a mating keyway 1417. When inserting the catheter into the drive assembly, the keyway 1415 on the handle initially aligns the spring-loaded handle lock bar boss 1419 with the keyway 1417, thereby allowing g for self-alignment of the handle with the drive assembly 1400. As the handle is inserted further, the handle lock bar boss 1419 eventually slides into a locking channel 1421 on the handle, securing the handle position. To release the handle, the user pushes the handle release button 1423, which can be attached to the handle lock bar 1411. As a result, the handle lock bar 1411 slides back into alignment with the keyway 1417, allowing the handle to be removed. Movement of the handle lock bar 1411 and button 1423 is otherwise restrained by the housing 1402.


Referring to FIGS. 12-13, the rotary optical subassembly 1411 includes a fiber optic rotating junction (FORJ) 1421 and a motor 1432, such as a DC brushless motor with integrated speed control. The rotary optical subassembly 1411 can be designed similar to the rotary optical subassembly 102 described above and can thus serve to both: (1) decouple the catheter fiber rotation from the source of rotation; and (2) drive the catheter's cutting and imaging elements through the optical connector 1427. The motor 1432 drives the FORJ 1421 through pulleys 1431, 1435 which are connected by a belt (not shown). In turn, the FORJ 1421 drives the rotation of the drive shaft and optical fiber of the catheter through the optical connector 1427.


The drive assembly 1400 can further include an automatic alignment feature to align the catheter properly with respect to the drive assembly 1400. Cleaving the optical fiber of the catheter and the optical fiber of the drive assembly at an angle (e.g. 8 degrees) is desirable to reduce back-reflection at the interface between the optical fibers. Immediate physical connection is also desirable to reduce transmission losses. As such, the optical fibers should be aligned at exactly the right orientation (with the angled cleaves lined up) to allow the light to travel from one optical fiber). If an automatic alignment feature is created to properly orient these fibers with respect to one another, then the separate step of manually connecting the optical assemblies of the catheter/handle and the drive assembly can be eliminated.


For example, referring to FIGS. 14A-14B, the drive assembly 1400 can be automatically aligned with the catheter handle through alignment mechanisms on both the drive assembly 1400 and on the catheter handle. Thus, in one embodiment, the drive assembly 1400 can include an orientation sensor 1433 configured to sense the rotational position of the optical connector 1427. For example, as shown in FIGS. 14A-14B, the sensor 1433 can be a slot sensor (or optical fork sensor) configured to detect a flag 1442 on the optical connector 1427. The sensor 1433 (in this case, a slot sensor) can thus detect as the flag 1442 passes therethrough. Because the flag 1442 is in a set position relative to the connection mechanisms of the optical connector 1427, the detection of the flag 1442 can allow for the determination of the rotational position or orientation of the connection mechanisms.


When the user powers the drive assembly 1400 off, a control board in the drive assembly 1400 can use feedback from the optical sensor 1433 to stop the motor 1432 such that the optical connector 1427 is always in the same position, such as the top-dead center position shown in FIG. 15. That is, after the user powers the drive assembly 1400 off, the control board can keep the motor 1432 and FORJ 1421 running at a constant speed until the exact position of the optical connector 1427 is identified based upon readings from the sensor 1433. The control board can then cut power to the motor such that, based upon the sensed position and the known length of time that the FORJ takes to stop after power is cut, the optical connector 1427 will stop in a predetermined position. The predetermine position can be the same every time that the drive assembly 1400 is used.


Advantageously, if the optical connector 1427 always stops in the same position, it can mate with a handle or catheter that is preset in a corresponding mating optical position (such as set by the manufacturer). Such a feature can provide for an automatic optical connection when the drive assembly is physically attached to the catheter or handle in a set orientation, such as with the locking mechanism described above. In some embodiments, the physical relationship between the drive assembly 1400 and the handle or catheter can be set, such as with a mating tooth (e.g. a protruding tooth or rib on the drive assembly and a recessed slot on the catheter handle).


Advantageously, the drive assembly 1400 can be less than 3 lbs, such as less than 2 lbs, such as approximately 1.5 lbs in weight. Further, the drive assembly can be less than 90 cubic inches, such as less than 75 cubic inches, such as less than 65 cubic inches, for example approximately 63 cubic inches in volume. In one embodiment, the drive assembly 1400 can measure 9″ by 3.5″ by 2″.


Another drive assembly 1700 is shown with respect to FIGS. 17-19 that can be configured to provide rotation of a drive shaft and rotation of an optical fiber of an imaging catheter.


Referring to FIG. 17, the drive assembly 1700 can include a housing 1701, an optical connector 1721 configured to connect the drive assembly 1700 to a light source, a power connector 1723 configured to connect the drive assembly 1700 to a power source, and a connection 1755 (such as the handle locks described above) configured to connect the drive assembly 1700 to a handle 900 of an imaging catheter.


As shown in FIG. 18A-19 the drive assembly 1700 can include a rotating optical drive subassembly 1811 including a FORJ 1813, a motor 1815, and an optical connector 1817, such as an MU adaptor, configured to connect the FORJ with the catheter drive shaft and optical fiber. The shaft of the motor 1815 can be hollow so as to allow the FORJ 1813 to extend therethrough (i.e., the motor 1815 and the FORJ 1813 can be coaxial). In one embodiment, as shown in FIG. 19, the FORJ 1813 is entirely on the stationary side of the motor, with only a rotating fiber 1993 passing through the motor 1815. In another embodiment, the FORJ 1813 works through the motor 1815, with a stationary fiber on one side, light passing through the hollow shaft, and a rotating fiber on the far side. In yet another embodiment, the FORJ 1813 is on the rotating side of the motor 1815 and a stationary fiber inside a stationary tube passes through the motor 1815. The motor 1815 can further be configured to provide sufficient torque without gearing. Further, the connector 1817 can be configured to as to minimize the moment of inertia and swept volume to reduce vibration.


Advantageously, by having the motor 1815 and the FORJ 1813 coaxial, the dimensions of the drive assembly 1700 can be reduced. For example, the drive assembly 1700 can have a volume of less than 40 cubic inches, such as less than 20 cubic inches, such as less than 18 cubic inches, such as approximately 14-16 cubic inches. Further, the drive assembly 1700 can have a length of less than or equal to nine inches and a diameter of less than or equal to 2.5 inches, such as approximately 1.25 inches. In exemplary embodiments, the drive assembly 1700 is approximately 9″ long by 1.5″ in diameter, 9″ long by 1.25″ in diameter, or 7″ long by 1.25″ in diameter.


Like the other drive assemblies described herein, when motor 1815 rotates, the FORJ 1813 can rotate, thereby causing the optical connector 1817 (and thus the drive shaft and optical fiber of the imaging catheter) to rotate. Further, similar to the drive assembly 1400, the drive assembly 1700 can include a mechanism for automatically/mechanically aligning the drive assembly 1700 with the handle or catheter, such as a top dead center sensor.


Referring to FIG. 19, it is to be understood that the FORJ 1815 (and any FORJ described herein) can include a rotating portion 1991 with a rotating fiber 1993 and a rotating lens 1995 and a stationary portion 1997 with a stationary fiber 1998 and a stationary lens 1999.


Referring to FIG. 16, in some embodiments, the drive assemblies described herein can include a magnetic handle locking assembly 2000 in place of the locking mechanisms described above. The locking assembly 2000 can be configured to mate with a magnetic assembly 2050 on the catheter handle.


In one embodiment, shown in FIG. 16, the locking assembly 2000 can include a magnetic housing 2002 and a female fiber optic connector 2004, such as an FC-APCC, which can be configured to mate with a catheter magnetic housing 2052 and a male fiber optic connector 2054, such as an FC-APC 2054 (though in other embodiments, the positions of the female/male FC-APCs could be reversed). The housings 2002, 2052 can include slots 2006a,b and 2056a,b configured to hold magnets therein. The magnets in each slot 2006a,b of the drive assembly can be of opposite polarity to one another. Further, the magnets in slots 2006a,b can be of opposite polarity to the magnets in the adjacent catheter locking assembly (e.g., magnets in slot 2006a can be of opposite polarity to magnets in slot 2056a). Thus, if the magnetic assemblies 2000, 2050 are not properly aligned, the opposing polarities of the magnets can cause the assemblies 2000, 2050 to rotate into the proper alignment, thus providing an automatic alignment feature for the drive assemblies described herein with a corresponding imaging catheter handle.


The locking assembly 2000 can further include mechanical teeth and mating slots 2063a,b therein configured to hold the magnetic assemblies 2000, 2050 together as one or the other is rotated, thereby transmitting torque from one assembly 2000 to the other 2050.


Advantageously, the magnetic handle locking assembly 2000 can allow insertion of the catheter into the drive assembly with a single hand without requiring a secondary fiber connection, in contrast to other drive assemblies where the optical connection was manually made after the mechanical connection was made.


The drive assemblies described herein can be reusable, advantageously reducing the cost and complexity associated with imaging catheters.


Further, the drive assemblies described herein can advantageously be introduced into the sterile field through use of a sterile bag. For example, a non-sterile operator, using sterile technique, can open the sterile bag pouch and present the sterile bag to the sterile operator. The sterile operator can remove the bag from the sterile pouch and pass the catheter handle through the sterile bag. The non-sterile operator can then present the drive assembly 100 to the sterile operator. The sterile operator can connect the catheter handle into the handle lock until the catheter is locked into place. The non-sterile operator can connect the optical connector 446 to the catheter and close the access door 107 of housing 101. The non-sterile operator can further grab the outside of the bag and pull the bag back over the drive assembly and attached cables. Finally, the sterile operator can position the bagged drive assembly in the sterile field where desired. The drive assembly can be activated through toggling of the power switch. Similar methodologies can be used with the drive assemblies 1400 and 1700 described herein, though the automatic optical connection between the drive assemblies 1400 and 1700 advantageously eliminates the step of creating a separate optical connection (such as by opening the access door 107 of the drive assembly 100).


It is to be understood that any of the features of the various exemplary drive assemblies described herein could be substituted or added to other drive assemblies while still lying within the scope of this disclosure.


The drive assemblies described herein can be used to transmit light from a source, such as for optical coherence tomography. Exemplary imaging systems that can be used with the drive assemblies are described in copending Patent Applications: U.S. patent application Ser. No. 12/790,703, titled “OPTICAL COHERENCE TOMOGRAPHY FOR BIOLOGICAL IMAGING,” filed May 28, 2010, Publication No. US-2010-0305452-A1; U.S. patent application Ser. No. 12/829,267, titled “CATHETER-BASED OFF-AXIS OPTICAL COHERENCE TOMOGRAPHY IMAGING SYSTEM,” filed Jul. 1, 2010, Publication No. US-2010-0021926-A1; and International Patent Application No. PCT/US2013/031951 titled “OPTICAL COHERENCE TOMOGRAPHY WITH GRADED INDEX FIBER FOR BIOLOGICAL IMAGING,” all of which are incorporated by reference in their entireties.


The drive assemblies described herein can be used with a variety of different catheters, such as atherectomy catheters with imaging. Exemplary catheters and/or handles that can be used with the drive assemblies described herein are set forth in U.S. Patent Applications: U.S. patent application Ser. No. 12/829,277, titled “ATHERECTOMY CATHETER WITH LATERALLY-DISPLACEABLE TIP,” filed Jul. 1, 2010, Publication No. US-2011-0004107-A1; U.S. patent application Ser. No. 13/175,232, titled “ATHERECTOMY CATHETERS WITH LONGITUDINALLY DISPLACEABLE DRIVE SHAFTS,” filed Jul. 1, 2011, Publication No. US-2012-0046679-A1; U.S. patent application Ser. No. 13/654,357, titled “ATHERECTOMY CATHETERS AND NON-CONTACT ACTUATION MECHANISM FOR CATHETERS,” filed Oct. 17, 2012; U.S. patent application Ser. No. 13/675,867, titled “OCCLUSION-CROSSING DEVICES, ATHERECTOMY DEVICES, AND IMAGING,” filed Nov. 13, 2012; International Patent Application No. PCT/US2013/031901 titled “ATHERECTOMY CATHETERS WITH IMAGING,” filed Mar. 15, 2013; and International Patent Application No. PCT/US2013/032494 titled “BALLOON ATHERECTOMY CATHETERS WITH IMAGING,” filed Mar. 15, 2013, all of which are incorporated by reference in their entireties.


Additional details pertinent to the present invention, including materials and manufacturing techniques, may be employed as within the level of those with skill in the relevant art. The same may hold true with respect to method-based aspects of the invention in terms of additional acts commonly or logically employed. Also, it is contemplated that any optional feature of the inventive variations described may be set forth and claimed independently, or in combination with any one or more of the features described herein. Likewise, reference to a singular item, includes the possibility that there are a plurality of the same items present. More specifically, as used herein and in the appended claims, the singular forms “a,” “and,” “said,” and “the” include plural referents unless the context clearly dictates otherwise. It is further noted that the claims may be drafted to exclude any optional element. As such, this statement is intended to serve as antecedent basis for use of such exclusive terminology as “solely,” “only” and the like in connection with the recitation of claim elements, or use of a “negative” limitation. Unless defined otherwise herein, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. The breadth of the present invention is not to be limited by the subject specification, but rather only by the plain meaning of the claim terms employed.


When a feature or element is herein referred to as being “on” another feature or element, it can be directly on the other feature or element or intervening features and/or elements may also be present. In contrast, when a feature or element is referred to as being “directly on” another feature or element, there are no intervening features or elements present. It will also be understood that, when a feature or element is referred to as being “connected”, “attached” or “coupled” to another feature or element, it can be directly connected, attached or coupled to the other feature or element or intervening features or elements may be present. In contrast, when a feature or element is referred to as being “directly connected”, “directly attached” or “directly coupled” to another feature or element, there are no intervening features or elements present. Although described or shown with respect to one embodiment, the features and elements so described or shown can apply to other embodiments. It will also be appreciated by those of skill in the art that references to a structure or feature that is disposed “adjacent” another feature may have portions that overlap or underlie the adjacent feature.


Terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. For example, as used herein, the singular forms “a”, “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms “comprises” and/or “comprising,” when used in this specification, specify the presence of stated features, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, steps, operations, elements, components, and/or groups thereof. As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items and may be abbreviated as “/”.


Spatially relative terms, such as “under”, “below”, “lower”, “over”, “upper” and the like, may be used herein for ease of description to describe one element or feature's relationship to another element(s) or feature(s) as illustrated in the figures. It will be understood that the spatially relative terms are intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the figures. For example, if a device in the figures is inverted, elements described as “under” or “beneath” other elements or features would then be oriented “over” the other elements or features. Thus, the exemplary term “under” can encompass both an orientation of over and under. The device may be otherwise oriented (rotated 90 degrees or at other orientations) and the spatially relative descriptors used herein interpreted accordingly. Similarly, the terms “upwardly”, “downwardly”, “vertical”, “horizontal” and the like are used herein for the purpose of explanation only unless specifically indicated otherwise.


Although the terms “first” and “second” may be used herein to describe various features/elements, these features/elements should not be limited by these terms, unless the context indicates otherwise. These terms may be used to distinguish one feature/element from another feature/element. Thus, a first feature/element discussed below could be termed a second feature/element, and similarly, a second feature/element discussed below could be termed a first feature/element without departing from the teachings of the present invention.


As used herein in the specification and claims, including as used in the examples and unless otherwise expressly specified, all numbers may be read as if prefaced by the word “about” or “approximately,” even if the term does not expressly appear. The phrase “about” or “approximately” may be used when describing magnitude and/or position to indicate that the value and/or position described is within a reasonable expected range of values and/or positions. For example, a numeric value may have a value that is +/−0.1% of the stated value (or range of values), +/−1% of the stated value (or range of values), +/−2% of the stated value (or range of values), +/−5% of the stated value (or range of values), +/−10% of the stated value (or range of values), etc. Any numerical range recited herein is intended to include all sub-ranges subsumed therein.

Claims
  • 1. A drive assembly for driving an imaging catheter having a rotatable fiber and a rotatable drive shaft, the drive assembly comprising: a drive assembly housing;a rotary optical subassembly within the housing and comprising a fiber optic rotating junction having a stationary portion with a stationary fiber therein and a rotatable portion with a rotatable fiber therein; anda linear slide within the housing, wherein the rotary optical subassembly rests on a translatable portion of the linear slide, the linear slide configured to translate the fiber optic rotating junction axially within the housing.
  • 2. The drive assembly of claim 1, wherein the linear slide comprises a stationary portion connected to the housing.
  • 3. The drive assembly of claim 1, wherein the translatable portion is movable relative to the housing.
  • 4. The drive assembly of claim 1, further comprising a locking mechanism on the housing configured to either allow or restrict the rotary optical subassembly from translating.
  • 5. The drive assembly of claim 1, further comprising a handle lock configured to secure a catheter handle of an imaging catheter assembly to the housing.
  • 6. The drive assembly of claim 1, wherein the translatable portion of the linear slide is configured to translate relative to the housing and to a catheter outer shaft, when the handle lock is secured to a catheter handle of the imaging catheter.
  • 7. The drive assembly of claim 1, wherein the stationary fiber of the fiber optic rotating junction includes slack configured to account for translation of the fiber optic rotating junction.
  • 8. The drive assembly of claim 7, wherein the linear slide comprises a space configured to receive the fiber optic rotating junction slack.
  • 9. The drive assembly of claim 1, wherein a volume of the drive assembly housing is less than 40 cubic inches, and wherein the drive assembly has a total weight of less than 2 pounds.
  • 10. A drive assembly for driving an imaging catheter having a rotatable fiber and a rotatable drive shaft, the drive assembly comprising: a drive assembly housing;a fiber optic rotating junction within the housing, the fiber optic rotating junction having a stationary portion with a stationary fiber therein and a rotatable portion with a rotatable fiber therein; anda linear slide in the housing, the linear slide configured to translate the fiber optic rotating junction axially within the housing, wherein the housing is less than 75 cubic inches in volume, and wherein the drive assembly has a total weight of less than 2 pounds.
CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 16/372,112, filed on Apr. 1, 2019, titled “ATHERECTOMY CATHETER DRIVE ASSEMBLIES,” now U.S. Pat. No. 11,206,975, which is a continuation of U.S. patent application Ser. No. 15/162,391, filed on May 23, 2016, titled “ATHERECTOMY CATHETER DRIVE ASSEMBLIES,” now U.S. Pat. No. 10,244,934, which is a continuation of U.S. patent application Ser. No. 14/400,151, filed on Nov. 10, 2014, titled “ATHERECTOMY CATHETER DRIVE ASSEMBLIES,” now U.S. Pat. No. 9,345,398, which is a 371 of International Patent Application No. PCT/US2013/032089, filed on Mar. 15, 2013, titled “ATHERECTOMY CATHETER DRIVE ASSEMBLIES,” now International Publication No. WO 2013/172974, which claims priority to U.S. Provisional Patent Application No. 61/646,843, filed on May 14, 2012, titled “ATHERECTOMY CATHETERS WITH IMAGING,” and U.S. Provisional Patent Application No. 61/697,743, filed on Sep. 6, 2012, titled “BALLOON ATHERECTOMY CATHETERS WITH IMAGING,” each of which is herein incorporated by reference in its entirety.

US Referenced Citations (586)
Number Name Date Kind
3367727 Ward et al. Feb 1968 A
3908637 Doroshow Sep 1975 A
4178935 Gekhaman et al. Dec 1979 A
4487206 Aagard Dec 1984 A
4527553 Upsher Jul 1985 A
4552554 Gould et al. Nov 1985 A
4578061 Lemelson Mar 1986 A
4598710 Kleinberg et al. Jul 1986 A
4611600 Cohen Sep 1986 A
4621353 Hazel et al. Nov 1986 A
4639091 Huignard et al. Jan 1987 A
4651753 Lifton Mar 1987 A
4654024 Crittenden et al. Mar 1987 A
4681106 Kensey et al. Jul 1987 A
4686982 Nash Aug 1987 A
4691708 Kane Sep 1987 A
4729763 Henrie Mar 1988 A
4771774 Simpson et al. Sep 1988 A
4781186 Simpson et al. Nov 1988 A
4808163 Laub Feb 1989 A
4841977 Griffith et al. Jun 1989 A
4842578 Johnson et al. Jun 1989 A
4850354 McGurk-Burleson et al. Jul 1989 A
4857046 Stevens et al. Aug 1989 A
4920961 Grossi et al. May 1990 A
4926858 Gifford, III et al. May 1990 A
5000185 Yock Mar 1991 A
5002560 Machold et al. Mar 1991 A
5018529 Tenerz et al. May 1991 A
5041082 Shiber Aug 1991 A
5047040 Simpson et al. Sep 1991 A
5085662 Willard Feb 1992 A
5099850 Matsui et al. Mar 1992 A
5178153 Einzig Jan 1993 A
5182291 Gubin et al. Jan 1993 A
5190050 Nitzsche Mar 1993 A
5192291 Pannek, Jr. Mar 1993 A
5217479 Shuler Jun 1993 A
5312415 Palermo May 1994 A
5312425 Evans et al. May 1994 A
5321501 Swanson et al. Jun 1994 A
5333142 Scheps Jul 1994 A
5358472 Vance et al. Oct 1994 A
5366464 Belknap Nov 1994 A
5372601 Lary Dec 1994 A
5383460 Jang et al. Jan 1995 A
5383467 Auer et al. Jan 1995 A
5425273 Chevalier Jun 1995 A
5425371 Mischenko Jun 1995 A
5429136 Milo et al. Jul 1995 A
5431673 Summers et al. Jul 1995 A
5437284 Trimble Aug 1995 A
5449372 Schmaltz et al. Sep 1995 A
5459570 Swanson et al. Oct 1995 A
5460168 Masubuchi et al. Oct 1995 A
5465147 Swanson Nov 1995 A
5507725 Savage et al. Apr 1996 A
5507760 Wynne et al. Apr 1996 A
5507795 Chiang et al. Apr 1996 A
5517998 Madison May 1996 A
5529580 Kusunok et al. Jun 1996 A
5556405 Lary Sep 1996 A
5607394 Andersen et al. Mar 1997 A
5613981 Boyle et al. Mar 1997 A
5620426 Braithwaite Apr 1997 A
5632754 Farley et al. May 1997 A
5632755 Nordgren et al. May 1997 A
5667490 Keith et al. Sep 1997 A
5674232 Halliburton Oct 1997 A
5676012 Ceriale Oct 1997 A
5681336 Clement et al. Oct 1997 A
5690634 Muller et al. Nov 1997 A
5722403 McGee et al. Mar 1998 A
5728148 Bostrom et al. Mar 1998 A
5749846 Edwards et al. May 1998 A
5795295 Hellmuth et al. Aug 1998 A
5807339 Bostrom et al. Sep 1998 A
5830145 Tenhoff Nov 1998 A
5836957 Schulz et al. Nov 1998 A
5843050 Jones et al. Dec 1998 A
5843103 Wulfman Dec 1998 A
5851212 Zirps et al. Dec 1998 A
5868778 Gershony et al. Feb 1999 A
5872879 Hamm Feb 1999 A
5904651 Swanson et al. May 1999 A
5907425 Dickensheets et al. May 1999 A
5935075 Casscells et al. Aug 1999 A
5935139 Bates Aug 1999 A
5938602 Lloyd Aug 1999 A
5938671 Katoh et al. Aug 1999 A
5951482 Winston et al. Sep 1999 A
5951581 Saadat et al. Sep 1999 A
5951583 Jensen et al. Sep 1999 A
5956355 Swanson et al. Sep 1999 A
5957952 Gershony et al. Sep 1999 A
5987995 Sawatari et al. Nov 1999 A
5997558 Nash Dec 1999 A
6001112 Taylor Dec 1999 A
6007530 Domhofer et al. Dec 1999 A
6010449 Selmon et al. Jan 2000 A
6013072 Winston et al. Jan 2000 A
6017359 Gershony et al. Jan 2000 A
6027514 Stine et al. Feb 2000 A
6032673 Savage et al. Mar 2000 A
6048349 Winston et al. Apr 2000 A
6080170 Nash et al. Jun 2000 A
6106515 Winston et al. Aug 2000 A
6110164 Vidlund Aug 2000 A
6120515 Rogers et al. Sep 2000 A
6120516 Selmon et al. Sep 2000 A
6134002 Stimson et al. Oct 2000 A
6134003 Tearney et al. Oct 2000 A
6152938 Curry Nov 2000 A
6152951 Hashimoto et al. Nov 2000 A
6160826 Swanson et al. Dec 2000 A
6175669 Colston et al. Jan 2001 B1
6176871 Pathak et al. Jan 2001 B1
6183432 Milo Feb 2001 B1
6193676 Winston et al. Feb 2001 B1
6206898 Honeycutt et al. Mar 2001 B1
6217549 Selmon et al. Apr 2001 B1
6228076 Winston et al. May 2001 B1
6241744 Imran et al. Jun 2001 B1
6283957 Hashimoto et al. Sep 2001 B1
6285903 Rosenthal et al. Sep 2001 B1
6290668 Gregory et al. Sep 2001 B1
6294775 Seibel et al. Sep 2001 B1
6299622 Snow et al. Oct 2001 B1
6307985 Murakami et al. Oct 2001 B1
6375615 Flaherty et al. Apr 2002 B1
6402719 Ponzi et al. Jun 2002 B1
6416527 Berg et al. Jul 2002 B1
6445939 Swanson et al. Sep 2002 B1
6445944 Ostrovsky Sep 2002 B1
6447525 Follmer et al. Sep 2002 B2
6451009 Dasilva et al. Sep 2002 B1
6451036 Heitzmann et al. Sep 2002 B1
6454717 Pantages et al. Sep 2002 B1
6454779 Taylor Sep 2002 B1
6482216 Hiblar et al. Nov 2002 B1
6482217 Pintor et al. Nov 2002 B1
6485413 Boppart et al. Nov 2002 B1
6497649 Parker et al. Dec 2002 B2
6501551 Teamey et al. Dec 2002 B1
6503261 Bruneau et al. Jan 2003 B1
6511458 Milo et al. Jan 2003 B2
6517528 Pantages et al. Feb 2003 B1
6542665 Reed et al. Apr 2003 B2
6544230 Flaherty et al. Apr 2003 B1
6546272 MacKinnon et al. Apr 2003 B1
6551302 Rosinko et al. Apr 2003 B1
6563105 Seibel et al. May 2003 B2
6564087 Pitris et al. May 2003 B1
6565588 Clement et al. May 2003 B1
6572563 Ouchi et al. Jun 2003 B2
6572643 Gharibadeh Jun 2003 B1
6575995 Huter et al. Jun 2003 B1
6579298 Bruneau et al. Jun 2003 B1
6599296 Gillick et al. Jul 2003 B1
6615071 Casscells, III et al. Sep 2003 B1
6629953 Boyd Oct 2003 B1
6638233 Corvi et al. Oct 2003 B2
6645217 MacKinnon et al. Nov 2003 B1
6657727 Izatt et al. Dec 2003 B1
6666874 Heitzmann et al. Dec 2003 B2
6673042 Samson et al. Jan 2004 B1
6687010 Horii Feb 2004 B1
6728571 Barbato Apr 2004 B1
D489973 Root et al. May 2004 S
6730063 Delaney et al. May 2004 B2
6758854 Butler et al. Jul 2004 B1
6760112 Reed et al. Jul 2004 B2
6800085 Selmon et al. Oct 2004 B2
6818001 Wulfman et al. Nov 2004 B2
6824550 Noriega et al. Nov 2004 B1
6830577 Nash et al. Dec 2004 B2
6845190 Smithwick et al. Jan 2005 B1
6852109 Winston et al. Feb 2005 B2
6853457 Bjarklev et al. Feb 2005 B2
6856712 Fauver et al. Feb 2005 B2
6867753 Chinthammit et al. Mar 2005 B2
6879851 McNamara et al. Apr 2005 B2
6947787 Webler Sep 2005 B2
6961123 Wang et al. Nov 2005 B1
6970732 Winston et al. Nov 2005 B2
6975898 Seibel Dec 2005 B2
7068878 Crossman-Bosworth et al. Jun 2006 B2
7074231 Jang Jul 2006 B2
7126693 Everett et al. Oct 2006 B2
7172610 Heitzmann et al. Feb 2007 B2
7242480 Alphonse Jul 2007 B2
7261687 Yang Aug 2007 B2
7288087 Winston et al. Oct 2007 B2
7291146 Steinke et al. Nov 2007 B2
7297131 Nita Nov 2007 B2
7311723 Seibel et al. Dec 2007 B2
7344546 Wulfman et al. Mar 2008 B2
7366376 Shishkov et al. Apr 2008 B2
7382949 Bouma et al. Jun 2008 B2
7426036 Feldchtein et al. Sep 2008 B2
7428001 Schowengerdt et al. Sep 2008 B2
7428053 Feldchtein et al. Sep 2008 B2
7455649 Root et al. Nov 2008 B2
7474407 Gutin Jan 2009 B2
7485127 Nistal Feb 2009 B2
7488340 Kauphusman et al. Feb 2009 B2
7530948 Seibel et al. May 2009 B2
7530976 MacMahon et al. May 2009 B2
7538859 Teamney et al. May 2009 B2
7538886 Feldchtein May 2009 B2
7539362 Teramura May 2009 B2
7542145 Toida et al. Jun 2009 B2
7544162 Ohkubo Jun 2009 B2
7545504 Buckland et al. Jun 2009 B2
7555333 Wang et al. Jun 2009 B2
7577471 Camus et al. Aug 2009 B2
7583872 Seibel et al. Sep 2009 B2
7616986 Seibel et al. Nov 2009 B2
7637885 Maschke Dec 2009 B2
7674253 Fisher et al. Mar 2010 B2
7682319 Martin et al. Mar 2010 B2
7706863 Imanishi et al. Apr 2010 B2
7728985 Feldchtein et al. Jun 2010 B2
7729745 Maschke Jun 2010 B2
7734332 Sher Jun 2010 B2
7738945 Fauver et al. Jun 2010 B2
7753852 Maschke Jul 2010 B2
7771425 Dycus et al. Aug 2010 B2
7776062 Bessellink et al. Aug 2010 B2
7785286 Magnin et al. Aug 2010 B2
7813609 Petersen et al. Oct 2010 B2
7821643 Amazeen et al. Oct 2010 B2
7824089 Charles Nov 2010 B2
7840283 Bush et al. Nov 2010 B1
7944568 Teramura et al. May 2011 B2
7952718 Li et al. May 2011 B2
7972299 Carter et al. Jul 2011 B2
8002763 Berthiaume et al. Aug 2011 B2
8059274 Splinter Nov 2011 B2
8062316 Patel et al. Nov 2011 B2
8068921 Prakash et al. Nov 2011 B2
8313493 Fisher Nov 2012 B2
8361097 Patel et al. Jan 2013 B2
8548571 He et al. Oct 2013 B2
8548603 Swoyer et al. Oct 2013 B2
8632557 Thatcher et al. Jan 2014 B2
8644913 Simpson et al. Feb 2014 B2
8647335 Markus Feb 2014 B2
8696695 Patel et al. Apr 2014 B2
8911459 Simpson et al. Dec 2014 B2
9119662 Moberg Sep 2015 B2
9125562 Spencer et al. Sep 2015 B2
9333007 Escudero et al. May 2016 B2
9345398 Tachibana et al. May 2016 B2
9345406 Spencer et al. May 2016 B2
9345510 Patel et al. May 2016 B2
9345511 Smith et al. May 2016 B2
9351757 Kusleika May 2016 B2
9498247 Patel et al. Nov 2016 B2
9498600 Rosenthal et al. Nov 2016 B2
9557156 Kankaria Jan 2017 B2
9572492 Simpson et al. Feb 2017 B2
9579157 Moberg Feb 2017 B2
9592075 Simpson et al. Mar 2017 B2
9642646 Patel et al. May 2017 B2
9788790 Black et al. Oct 2017 B2
9854979 Smith et al. Jan 2018 B2
9918734 Patel et al. Mar 2018 B2
9949754 Newhauser et al. Apr 2018 B2
10052125 Rosenthal et al. Aug 2018 B2
10130386 Simpson et al. Nov 2018 B2
10244934 Tachibana et al. Apr 2019 B2
10335173 Carver et al. Jul 2019 B2
10342491 Black et al. Jul 2019 B2
10349974 Patel et al. Jul 2019 B2
10357277 Patel et al. Jul 2019 B2
10363062 Spencer et al. Jul 2019 B2
10406316 Garvey et al. Sep 2019 B2
10470795 Patel et al. Nov 2019 B2
10548478 Simpson et al. Feb 2020 B2
10568520 Patel et al. Feb 2020 B2
10568655 Simpson et al. Feb 2020 B2
10722121 Smith et al. Jul 2020 B2
10729326 Spencer et al. Aug 2020 B2
10806484 Simpson et al. Oct 2020 B2
10860484 Simpson et al. Oct 2020 B2
10869685 Patel et al. Dec 2020 B2
10932670 Smith et al. Mar 2021 B2
10952615 Kankaria Mar 2021 B2
10952763 Newhauser et al. Mar 2021 B2
11033190 Patel et al. Jun 2021 B2
11076773 Patel et al. Aug 2021 B2
11096717 Gupta et al. Aug 2021 B2
11134849 Simpson et al. Oct 2021 B2
11135019 Spencer et al. Oct 2021 B2
11147583 Patel et al. Oct 2021 B2
11206975 Tachibana et al. Dec 2021 B2
11224459 Patel et al. Jan 2022 B2
11278248 Christensen Mar 2022 B2
11284839 Black et al. Mar 2022 B2
11284916 Patel et al. Mar 2022 B2
20010005788 McGuckin, Jr. Jun 2001 A1
20010020126 Swanson et al. Sep 2001 A1
20020019644 Hastings et al. Feb 2002 A1
20020072706 Hiblar et al. Jun 2002 A1
20020082585 Carroll et al. Jun 2002 A1
20020082626 Donohoe et al. Jun 2002 A1
20020097400 Jung et al. Jul 2002 A1
20020111548 Swanson et al. Aug 2002 A1
20020115931 Strauss et al. Aug 2002 A1
20020138091 Pflueger Sep 2002 A1
20020147459 Bashiri et al. Oct 2002 A1
20020158547 Wood Oct 2002 A1
20030002038 Mawatari Jan 2003 A1
20030028100 Tearney et al. Feb 2003 A1
20030032880 Moore Feb 2003 A1
20030045835 Anderson et al. Mar 2003 A1
20030095248 Frot May 2003 A1
20030097044 Rovegno May 2003 A1
20030114875 Sjostrom Jun 2003 A1
20030120150 Govari Jun 2003 A1
20030120295 Simpson et al. Jun 2003 A1
20030125756 Shturman et al. Jul 2003 A1
20030125757 Patel et al. Jul 2003 A1
20030125758 Simpson et al. Jul 2003 A1
20030139751 Evans et al. Jul 2003 A1
20030163085 Tanner Aug 2003 A1
20030181855 Simpson et al. Sep 2003 A1
20040002650 Mandrusov et al. Jan 2004 A1
20040039371 Tockman et al. Feb 2004 A1
20040057667 Yamada et al. Mar 2004 A1
20040059257 Gaber Mar 2004 A1
20040082850 Bonner et al. Apr 2004 A1
20040092915 Levatter May 2004 A1
20040093001 Hamada May 2004 A1
20040147934 Kiester Jul 2004 A1
20040167553 Simpson et al. Aug 2004 A1
20040167554 Simpson et al. Aug 2004 A1
20040181249 Torrance et al. Sep 2004 A1
20040186368 Ramzipoor et al. Sep 2004 A1
20040193140 Griffin et al. Sep 2004 A1
20040202418 Ghiron et al. Oct 2004 A1
20040220519 Wulfman et al. Nov 2004 A1
20040230212 Wulfman Nov 2004 A1
20040230213 Wulfman et al. Nov 2004 A1
20040236312 Nistal et al. Nov 2004 A1
20040243162 Wulfman et al. Dec 2004 A1
20040254599 Lipoma et al. Dec 2004 A1
20040260236 Manning et al. Dec 2004 A1
20050020925 Kleen et al. Jan 2005 A1
20050021075 Bonnette et al. Jan 2005 A1
20050027199 Clarke Feb 2005 A1
20050043614 Huizenga et al. Feb 2005 A1
20050054947 Goldenberg Mar 2005 A1
20050075660 Chu et al. Apr 2005 A1
20050085708 Fauver et al. Apr 2005 A1
20050085721 Fauver et al. Apr 2005 A1
20050105097 Fang-Yen et al. May 2005 A1
20050141843 Warden et al. Jun 2005 A1
20050149096 Hilal et al. Jul 2005 A1
20050154407 Simpson Jul 2005 A1
20050159712 Andersen Jul 2005 A1
20050159731 Lee Jul 2005 A1
20050171478 Selmon et al. Aug 2005 A1
20050177068 Simpson Aug 2005 A1
20050182295 Soper et al. Aug 2005 A1
20050187571 Maschke Aug 2005 A1
20050192496 Maschke Sep 2005 A1
20050197623 Leeflang et al. Sep 2005 A1
20050201662 Petersen et al. Sep 2005 A1
20050203553 Maschke Sep 2005 A1
20050222519 Simpson Oct 2005 A1
20050222663 Simpson et al. Oct 2005 A1
20050251116 Steinke et al. Nov 2005 A1
20060011820 Chow-Shing et al. Jan 2006 A1
20060032508 Simpson Feb 2006 A1
20060046235 Alexander Mar 2006 A1
20060049587 Cornwell Mar 2006 A1
20060064009 Webler et al. Mar 2006 A1
20060084911 Belef et al. Apr 2006 A1
20060109478 Tearney et al. May 2006 A1
20060135870 Webler Jun 2006 A1
20060173475 Lafontaine et al. Aug 2006 A1
20060229646 Sparks Oct 2006 A1
20060229659 Gifford et al. Oct 2006 A1
20060235262 Arnal et al. Oct 2006 A1
20060235366 Simpson Oct 2006 A1
20060236019 Soito et al. Oct 2006 A1
20060239982 Simpson Oct 2006 A1
20060241503 Schmitt et al. Oct 2006 A1
20060244973 Yun et al. Nov 2006 A1
20060252993 Freed et al. Nov 2006 A1
20060264741 Prince Nov 2006 A1
20060264743 Kleen et al. Nov 2006 A1
20060264907 Eskridge et al. Nov 2006 A1
20070010840 Rosenthal et al. Jan 2007 A1
20070015969 Feldman et al. Jan 2007 A1
20070015979 Redel Jan 2007 A1
20070035855 Dickensheets Feb 2007 A1
20070038061 Huennekens et al. Feb 2007 A1
20070038125 Kleen et al. Feb 2007 A1
20070038173 Simpson Feb 2007 A1
20070050019 Hyde Mar 2007 A1
20070078469 Soito et al. Apr 2007 A1
20070078500 Ryan et al. Apr 2007 A1
20070081166 Brown et al. Apr 2007 A1
20070088230 Terashi et al. Apr 2007 A1
20070106155 Goodnow et al. May 2007 A1
20070135712 Maschke Jun 2007 A1
20070167710 Unal et al. Jul 2007 A1
20070196926 Soito et al. Aug 2007 A1
20070213618 Li et al. Sep 2007 A1
20070219484 Straub Sep 2007 A1
20070250080 Jones et al. Oct 2007 A1
20070255252 Mehta Nov 2007 A1
20070270647 Nahen et al. Nov 2007 A1
20070276419 Rosenthal Nov 2007 A1
20070288036 Seshadri Dec 2007 A1
20070299309 Seibel et al. Dec 2007 A1
20080004643 To et al. Jan 2008 A1
20080004644 To et al. Jan 2008 A1
20080004645 To et al. Jan 2008 A1
20080004646 To et al. Jan 2008 A1
20080015491 Bel et al. Jan 2008 A1
20080015618 Sonnenschein et al. Jan 2008 A1
20080027334 Langston Jan 2008 A1
20080033396 Danek et al. Feb 2008 A1
20080045986 To et al. Feb 2008 A1
20080049234 Seitz Feb 2008 A1
20080058629 Seibel et al. Mar 2008 A1
20080065124 Olson Mar 2008 A1
20080065125 Olson Mar 2008 A1
20080065205 Nguyen et al. Mar 2008 A1
20080095421 Sun et al. Apr 2008 A1
20080103439 Torrance et al. May 2008 A1
20080103446 Torrance et al. May 2008 A1
20080103516 Wulfman et al. May 2008 A1
20080132929 O'Sullivan et al. Jun 2008 A1
20080139897 Ainsworth et al. Jun 2008 A1
20080146942 Dala-Krishna Jun 2008 A1
20080147000 Seibel et al. Jun 2008 A1
20080154293 Taylor et al. Jun 2008 A1
20080154296 Taylor et al. Jun 2008 A1
20080177138 Courtney et al. Jul 2008 A1
20080186501 Xie Aug 2008 A1
20080207996 Tsai Aug 2008 A1
20080221388 Seibel et al. Sep 2008 A1
20080228033 Tumlinson et al. Sep 2008 A1
20080243030 Seibel et al. Oct 2008 A1
20080243031 Seibel et al. Oct 2008 A1
20080262312 Carroll et al. Oct 2008 A1
20080275485 Bonnette et al. Nov 2008 A1
20080287795 Klingensmith et al. Nov 2008 A1
20090018565 To et al. Jan 2009 A1
20090018566 Escudero et al. Jan 2009 A1
20090018567 Escudero et al. Jan 2009 A1
20090024084 Khosla et al. Jan 2009 A1
20090024085 To et al. Jan 2009 A1
20090024191 Seibel et al. Jan 2009 A1
20090028407 Seibel et al. Jan 2009 A1
20090028507 Jones et al. Jan 2009 A1
20090043191 Castella et al. Feb 2009 A1
20090073444 Wang Mar 2009 A1
20090073455 Onimura Mar 2009 A1
20090076447 Casas et al. Mar 2009 A1
20090093764 Pfeffer et al. Apr 2009 A1
20090099641 Wu et al. Apr 2009 A1
20090125019 Douglass et al. May 2009 A1
20090135280 Johnston et al. May 2009 A1
20090137893 Seibel et al. May 2009 A1
20090152664 Tian et al. Jun 2009 A1
20090185135 Volk Jul 2009 A1
20090196477 Cense Aug 2009 A1
20090196554 Irisawa Aug 2009 A1
20090198125 Nakabayashi et al. Aug 2009 A1
20090208143 Yoon et al. Aug 2009 A1
20090216180 Lee et al. Aug 2009 A1
20090221904 Shealy et al. Sep 2009 A1
20090221920 Boppart et al. Sep 2009 A1
20090234220 Maschke Sep 2009 A1
20090235396 Wang et al. Sep 2009 A1
20090244485 Walsh et al. Oct 2009 A1
20090244547 Ozawa Oct 2009 A1
20090264826 Thompson Oct 2009 A1
20090268159 Xu et al. Oct 2009 A1
20090275966 Mitusina Nov 2009 A1
20090284749 Johnson et al. Nov 2009 A1
20090292199 Bielewicz et al. Nov 2009 A1
20090306520 Schmitt et al. Dec 2009 A1
20090316116 Melville et al. Dec 2009 A1
20090318862 Ali et al. Dec 2009 A1
20100004544 Toida Jan 2010 A1
20100021926 Noordin Jan 2010 A1
20100049225 To et al. Feb 2010 A1
20100080016 Fukui et al. Apr 2010 A1
20100082000 Honeck et al. Apr 2010 A1
20100125253 Olson May 2010 A1
20100130996 Doud et al. May 2010 A1
20100198081 Hanlin et al. Aug 2010 A1
20100217245 Prescott Aug 2010 A1
20100241147 Maschke Sep 2010 A1
20100253949 Adler et al. Oct 2010 A1
20100292539 Lankenau et al. Nov 2010 A1
20100292721 Moberg Nov 2010 A1
20100312263 Moberg et al. Dec 2010 A1
20100317973 Nita Dec 2010 A1
20100324472 Wulfman Dec 2010 A1
20110023617 Yu et al. Feb 2011 A1
20110028977 Rauscher et al. Feb 2011 A1
20110040238 Wulfman et al. Feb 2011 A1
20110058250 Liu et al. Mar 2011 A1
20110060186 Tilson et al. Mar 2011 A1
20110071401 Hastings et al. Mar 2011 A1
20110092955 Purdy et al. Apr 2011 A1
20110106004 Eubanks et al. May 2011 A1
20110118660 Torrance et al. May 2011 A1
20110130777 Zhang et al. Jun 2011 A1
20110137140 Teamney et al. Jun 2011 A1
20110144673 Zhang et al. Jun 2011 A1
20110201924 Tearney et al. Aug 2011 A1
20110208222 Ljahnicky et al. Aug 2011 A1
20110257478 Kleiner et al. Oct 2011 A1
20110264125 Wilson et al. Oct 2011 A1
20110270187 Nelson Nov 2011 A1
20110295148 Destoumieux et al. Dec 2011 A1
20110301625 Mauch et al. Dec 2011 A1
20110319905 Palme et al. Dec 2011 A1
20120002928 Irisawa Jan 2012 A1
20120004506 Tearney et al. Jan 2012 A1
20120123352 Fruland et al. May 2012 A1
20120136350 Goshgarian et al. May 2012 A1
20120203230 Adams Aug 2012 A1
20120238869 Schmitt et al. Sep 2012 A1
20120259337 del Rio et al. Oct 2012 A1
20120277730 Salahieh et al. Nov 2012 A1
20120289971 Segermark et al. Nov 2012 A1
20130023865 Steinke et al. Jan 2013 A1
20130035692 Sorensen et al. Feb 2013 A1
20130072787 Wallace et al. Mar 2013 A1
20130184549 Avitall et al. Jul 2013 A1
20130211221 Sunnarborg et al. Aug 2013 A1
20130223798 Jenner et al. Aug 2013 A1
20130223801 Bhagavatula et al. Aug 2013 A1
20130255069 Higashi et al. Oct 2013 A1
20130266259 Bhagavatula et al. Oct 2013 A1
20130287282 Yokota et al. Oct 2013 A1
20130317519 Romo et al. Nov 2013 A1
20130325003 Kapur et al. Dec 2013 A1
20130331819 Rosenman et al. Dec 2013 A1
20140005534 He et al. Jan 2014 A1
20140046250 Jain et al. Feb 2014 A1
20140128893 Guggenheimer et al. May 2014 A1
20140187949 Zhao et al. Jul 2014 A1
20140222042 Kessler et al. Aug 2014 A1
20140222047 Vreeman Aug 2014 A1
20140275996 Stigall Sep 2014 A1
20140371718 Alvarez et al. Dec 2014 A1
20150025310 Everingham et al. Jan 2015 A1
20150141816 Gupta et al. May 2015 A1
20150320975 Simpson et al. Nov 2015 A1
20160144155 Simpson et al. May 2016 A1
20180207417 Zung et al. Jul 2018 A1
20190029714 Patel et al. Jan 2019 A1
20190110809 Rosenthal et al. Apr 2019 A1
20190313941 Radjabi Oct 2019 A1
20200060718 Patel et al. Feb 2020 A1
20200323553 Fernandez et al. Oct 2020 A1
20210059713 Patel et al. Mar 2021 A1
20210076949 Smith et al. Mar 2021 A1
20210177262 Spencer et al. Jun 2021 A1
20210267621 Simpson et al. Sep 2021 A1
20210330345 Newhauser et al. Oct 2021 A1
20210345903 Patel et al. Nov 2021 A1
20220007941 Kankaria Jan 2022 A1
20220031168 Patel et al. Feb 2022 A1
20220039658 Smith et al. Feb 2022 A1
20220039828 Patel et al. Feb 2022 A1
20220071656 Patel et al. Mar 2022 A1
20220168011 Patel et al. Jun 2022 A1
20220273336 Fernandez et al. Sep 2022 A1
20220273337 Patel et al. Sep 2022 A1
20230225616 Patel et al. Jul 2023 A1
20240057942 Black et al. Feb 2024 A1
20240122479 Smith et al. Apr 2024 A1
20240148253 Simpson et al. May 2024 A1
20240180584 Patel et al. Jun 2024 A1
Foreign Referenced Citations (94)
Number Date Country
1875242 Dec 2006 CN
1947652 Apr 2007 CN
101601581 Dec 2009 CN
103027727 Apr 2013 CN
104968285 Oct 2015 CN
202006018883.5 Feb 2007 DE
0347098 Dec 1989 EP
0808638 Nov 1997 EP
0845692 Nov 2005 EP
1859732 Nov 2007 EP
2090245 Aug 2009 EP
2353526 Sep 2013 EP
S62-275425 Nov 1987 JP
03502060 Feb 1990 JP
H05501065 Mar 1993 JP
05103763 Apr 1993 JP
06027343 Feb 1994 JP
H07184888 Jul 1995 JP
07308393 Nov 1995 JP
2002214127 Jul 2002 JP
2004509695 Apr 2004 JP
2004516073 Jun 2004 JP
2005114473 Apr 2005 JP
2005230550 Sep 2005 JP
2005249704 Sep 2005 JP
2005533533 Nov 2005 JP
2008175698 Jul 2006 JP
2006288775 Oct 2006 JP
2006313158 Nov 2006 JP
2006526790 Nov 2006 JP
2006326157 Dec 2006 JP
200783053 Apr 2007 JP
200783057 Apr 2007 JP
2007225349 Sep 2007 JP
2007533361 Nov 2007 JP
2008023627 Feb 2008 JP
2008128708 Jun 2008 JP
2008145376 Jun 2008 JP
2008183208 Aug 2008 JP
2008253492 Oct 2008 JP
200914751 Jan 2009 JP
2009509690 Mar 2009 JP
200978150 Apr 2009 JP
2009066252 Apr 2009 JP
2009201969 Sep 2009 JP
2010042182 Feb 2010 JP
2010518900 Jun 2010 JP
2011517601 Jun 2011 JP
2011521747 Jul 2011 JP
2012143558 Aug 2012 JP
2012229976 Nov 2012 JP
2012533353 Dec 2012 JP
2013512736 Apr 2013 JP
2013524930 Jun 2013 JP
2015533584 Nov 2015 JP
2016508758 Mar 2016 JP
20070047221 May 2007 KR
218585902 Jul 2002 RU
2218191 Dec 2003 RU
WO9117698 Nov 1991 WO
WO9923958 May 1999 WO
WO0054659 Sep 2000 WO
WO0115609 Mar 2001 WO
WO0176680 Oct 2001 WO
WO2006133030 Dec 2006 WO
WO2008005888 Jan 2008 WO
WO2008029506 Mar 2008 WO
WO2008042987 Apr 2008 WO
WO2008051951 May 2008 WO
WO2008065600 Jun 2008 WO
WO2008086613 Jul 2008 WO
WO2008087613 Jul 2008 WO
WO2008151155 Dec 2008 WO
WO2009005779 Jan 2009 WO
WO2009006335 Jan 2009 WO
WO2009009799 Jan 2009 WO
WO2009009802 Jan 2009 WO
VO2009023635 Feb 2009 WO
WO2009024344 Feb 2009 WO
WO2009094341 Jul 2009 WO
WO2009140617 Nov 2009 WO
WO2009148317 Dec 2009 WO
WO2010039464 Apr 2010 WO
WO2010056771 May 2010 WO
WO2011044387 Apr 2011 WO
WO2011062087 May 2011 WO
WO2012057940 May 2012 WO
WO2012061935 May 2012 WO
WO2012123737 Sep 2012 WO
WO2012166332 Dec 2012 WO
WO2013033490 Mar 2013 WO
WO2013056262 Apr 2013 WO
WO2014077870 May 2014 WO
WO2014093148 Jun 2014 WO
Non-Patent Literature Citations (33)
Entry
Rosenthal et al.; U.S. Appl. No. 18/337,852 entitled “Atherectomy catheter with laterally-displaceable tip,” filed Jun. 20, 2023.
Patel et al.; U.S. Appl. No. 18/550,243 entitled “Occlusion-crossing devices,” filed Sep. 12, 2023.
Patel; U.S. Appl. No. 18/480,452 entitled “Occlusion-crossing devices,” filed Oct. 3, 2023.
Aziz et al.; Chronic total occlusions—a stiff challege requiring a major breakthrough: is there light at the end of the tunnel?; Heart; vol. 91; suppl. III; pp. 42-48; Jun. 2005.
Bayer Material Science: : Snap-Fit Joints for Plastics; 26 pages; retrieved from the Internet: (https://web.archive.org/web/20121119232733if_/http://fab.cba.mit.edu:80/classes/S62.12/people/vernelle.noel/Plastic_ Snap_fit_design.pdf) on Sep. 26, 2018.
Choma et al.; Sensitivity advantage of swept source and fourier domain optical coherence tomography; Optics Express; 11(18); pp. 2183-2189; Sep. 8, 2003.
De Boer et al.; Improved signal-to-noise ratio in spectral-domain compared with time-domain optical coherence tomography; Optics Letters; 28(21); pp. 2067-2069; Nov. 2003.
Emkey et al.; Analysis and evaluation of graded-index fiber-lenses; Journal of Lightwave Technology; vol. LT-5; No. 9; pp. 1156-1164; Sep. 1987.
Gonzalo et al.; Optical coherence tomography patterns of stent restenosis; Am. Heart J.; 158(2); pp. 284-293; Aug. 2009.
Han et al.; In situ Frog Retina Imaging Using Common-Path OCT with a Gold-Coated Bare Fiber Probe; CFM6; San Jose, California; CLEO, May 4, 2008; 2 pages.
Leitgeb et al.; Performance of fourier domain vs time domain optical coherence tomography; Optics Express; 11(8); pp. 889-894; Apr. 21, 2003.
Linares et al.; Arbitrary single-mode coupling by tapered and nontapered grin fiber lenses; Applied Optics; vol. 29; No. 28; pp. 4003-4007; Oct. 1, 1990.
Merriam Webster; Proximal (Definition); 10 pages; retrieved from the internet (https://www.merriam-webster.com/dictionary/proximal) on Jun. 9, 2021.
Muller et al.; Time-gated infrared fourier-domain optical coherence tomography; CFM5; San Jose, California; CLEO May 4, 2008; 2 pages.
Rollins et al.; Optimal interferometer designs for optical coherence tomography; Optics Letters; 24(21); pp. 1484-1486; Nov. 1999.
Schmitt et al.; A new rotational thrombectomy catheter: System design and first clinical experiences; Cardiovascular and Interventional Radiology; Springer-Verlag; 22(6); pp. 504-509; Nov. 1, 1999.
Sharma et al.; Common-path optical coherence tomography with side-viewing bare fiber probe for endoscopic optical coherence tomography; Rev. Sci. Instrum.; vol. 78; 113102; 5 pages: Nov. 6, 2007.
Sharma et al.; Optical coherence tomography based on an all-fiber autocorrelator using probe-end reflection as reference; CWJ13; San Francisco, California; CLEO May 16, 2004; 4 pages.
Shinkle et al.; Evaluation of stent placement and outcomes with optical coherence tomography; Interv. Cardiol.; 2(4); pp. 535-543; (manuscript version, 12 pages); Aug. 2010.
Stamper et al.; Plaque characterization with optical coherence tomography. Journal of the American College of Cardiology. 47(8); pp. 69-79; Apr. 18, 2006.
Suparno et al.; Light scattering with single-mode fiber collimators; Applied Optics; vol. 33; No. 30; pp. 7200-7205; Oct. 20, 1994.
Tanaka et al.; Challenges on the frontier of intracoronary imaging: atherosclerotic plaque macrophage measurement by optical coherence tomography; Journal of Biomedical Optics; 15(1); pp.(011104-1)-(011104-8); Jan.-Feb. 2010.
Wang et al.; Common-path endoscopic Fourier domain OCT with a reference Michelson interferometer; Proceedings of the SPIE; vol. 7566; pp. 75660L-75660L-7; Jan. 2010.
Wikipedia; Hinge; 4 pages; retrieved from the internet (https://en.wikipedia.org/w/index.php?title=Hinge&oldid=479569345) on Jun. 9, 2021.
Gupta et al.; U.S. Appl. No. 17/445,648 entitled “Tissue collection device for catheter,” filed Aug. 23, 2021.
Simpson et al.; U.S. Appl. No. 17/449,867 entitled “Occlusion-crossing devices, imaging, and atherectomy devices,” filed Oct. 4, 2021.
Spencer et al.; U.S. Appl. No. 17/449,895 entitled “Occlusion-crossing devices, atherectomy devices, and imaging,” filed Oct. 4, 2021.
Patel et al.; U.S. Appl. No. 17/816,673 entitled “Atherectomy catheter with serrated cutter,” filed Aug. 1, 2022.
Black et al.; U.S. Appl. No. 17/652,073 entitled “Optical coherence tomography for biological imaging,” filed Feb. 22, 2022.
Patel et al.; U.S. Appl. No. 17/762,815 entitled “Atherectomy catheter with shapeable distal tip,” filed Mar. 23, 2022.
Patel et al.; U.S. Appl. No. 17/763,810 entitled “Occlusion-crossing devices,” filed Mar. 25, 2022.
Simpson et al.; U.S. Appl. No. 18/582,526 entitled “Identification of elastic lamina to guide interventional therapy,” filed Feb. 20, 2024.
Patel.; U.S. Appl. No. 18/716,831 entitled “Atherectomy catheter with shapeable distal tip,” filed Jun. 5, 2024.
Related Publications (1)
Number Date Country
20220183545 A1 Jun 2022 US
Provisional Applications (2)
Number Date Country
61697743 Sep 2012 US
61646843 May 2012 US
Continuations (3)
Number Date Country
Parent 16372112 Apr 2019 US
Child 17645722 US
Parent 15162391 May 2016 US
Child 16372112 US
Parent 14400151 US
Child 15162391 US