# US 11,896,259 B2 · Atherectomy device and method > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 11,896,259 B2 - Document ID: US11896259B2 - Status: Granted - Kind: B2 - Application number: 16/693,822 - Filed: 2019-11-25 - Published: 2020-05-21 - Granted: 2024-02-13 - Earliest claimed: 2017-05-30 - Assignees: Terumo Kabushiki Kaisha - Applicants: Terumo Kabushiki Kaisha - Inventors: Tomonori Hatta; Kousuke Nishio; Taiga Nakano; Junichi Kobayashi - Web page: https://patentgrep.com/patent/US11896259B2 ## CPC - A61B 17/320758: {with a rotating cutting instrument, e.g. motor driven (A61B17/320725, A61B17/32075 and A61B17/320783 take precedence; for removing intra-ocular material A61F9/00763; endoscopic rotatable cutting instruments A61B17/32002)} - A61B 2017/00309: {Cut-outs or slits} - A61B 2017/00314: {Separate linked members} - A61B 2017/00323: {Cables or rods} - A61B 2017/00327: {with actuating members moving in opposite directions} - A61B 2017/00331: {with preformed bends} - A61B 2017/00398: {using powered actuators, e.g. stepper motors, solenoids} - A61B 2017/00734: {battery operated} - A61B 2017/00738: {part of the tool being offset with respect to a main axis, e.g. for better view for the surgeon} - A61B 2017/00867: {shape memory effect} - A61B 2017/320733: {with a flexible cutting or scraping element, e.g. with a whip-like distal filament member} - A61B 2217/005: with suction drainage system - A61B: DIAGNOSIS; SURGERY; IDENTIFICATION (usefulness limited to only animals A61D) ## Abstract A medical device is disclosed, the medical device includes an outer tubular member made from one or more rigid materials having a first bend element including a distal end portion of the outer tubular member and a second bend element proximal to the first bend element in a natural state; and a treatment member on the distal end portion configured to grind a substance inside a body lumen, and wherein an outer diameter of the treatment member is larger than an outer diameter of the outer tubular member, and a difference between the outer diameter of the treatment member and the outer diameter of the outer tubular member is less than a thickness of a blood vessel wall. ## Claims ### Claim 1 A medical device, the medical device comprising: an outer tubular member made from one or more rigid materials having a first bend element and a second bend element, the second bend element being proximal to the first bend element in a natural state; a drive shaft and a rotatable treatment member configured to be accommodated in the outer tubular member, the treatment member on a distal end of the drive shaft, the treatment member configured to rotate and grind a substance inside a body lumen, the treatment member including a distal-most end portion, a proximal end portion, and an intermediate portion positioned axially between the distal-most end portion and the proximal end portion, and wherein the intermediate portion tapers toward the distal-most end portion of the treatment member from a proximal-most end of the intermediate portion to a distal-most end of the intermediate portion, and wherein the distal-most end portion, the proximal end portion, and the intermediate portion are configured to be exposed distally beyond a distal end of the outer tubular member and configured to grind the substance inside the body lumen, and at least a portion of the distal-most end portion and at least a portion of the intermediate portion includes a coating configured to help facilitate the grinding of the substance inside the body lumen; and the treatment member including at least one window that communicates with a lumen of the outer tubular member, and wherein the lumen of the outer tubular member is in communication with an aspiration tube configured to be connected to an aspiration source. ### Claim 2 (depends on 1) The medical device of claim 1, wherein the first bend element and the second bend element are configured to contact a vessel wall at a same time such that the first bend element is configured to redirect a tip of the treatment member in order not to face the tip toward the vessel wall and the second bend element is configured to enhance a contact force against the vessel wall on an opposite side of at least the first bend element. ### Claim 3 (depends on 1) The medical device of claim 1, wherein the first bend element and the treatment member are configured to be substantially coplanar in a state of contact with a blood vessel wall. ### Claim 4 (depends on 1) The medical device of claim 1, wherein in the natural state or a packaged state, and where d is an outer diameter of the outer tubular member, h is an inner diameter of a target blood vessel lumen, θ1 is an angle in degrees of the first bend element, θ2 is an angle in degrees of the second bend element, and l is a length between the first bend element and the second bend element, and wherein θ1 is equal to θ2. ### Claim 5 (depends on 1) The medical device of claim 1, wherein in the natural state or a packaged state, and where d is an outer diameter of the outer tubular member, h is an inner diameter of a target blood vessel lumen, θ1 is an angle in degrees of the first bend element, θ2 is an angle in degrees of the second bend element, and l is a length between the first bend element and the second bend element, in case of θ1=θ2, the medical device is configured to work in a vessel that has the an inner diameter less than h; in case of θ1>θ2, the medical device is configured to work in the vessel that has the inner diameter greater than h; and in case of θ1<θ2, a tip of the treatment member is configured to face toward an inside the vessel. ### Claim 6 (depends on 1) The medical device of claim 1, wherein the outer tubular member is comprised a first tubular member and a second tubular member, the first tubular member being Nitinol and the second tubular member being stainless steel, and a connector between the first tubular member and the second tubular member. ### Claim 7 (depends on 6) The medical device of claim 6, wherein a rigidity of a distal end of the first tubular member is higher than a rigidity of the first bend element. ### Claim 8 (depends on 6) The medical device of claim 6, wherein the first bend element and the second bend element are located in the first tubular member. ### Claim 9 (depends on 6) The medical device of claim 6, wherein the connector is located on a straight part of the outer tubular member. ### Claim 10 (depends on 1) The medical device of claim 1, wherein the first bend element, the second bend element, and the treatment member are configured to helically contact a blood vessel wall. ### Claim 11 (depends on 1) The medical device of claim 1, wherein the outer tubular member is configured to rotate while maintaining a state in which a guide wire does not rotate with the first bend element, the second bend element, and the treatment member are in a state of contact with a vessel wall. ### Claim 12 (depends on 1) The medical device of claim 1, wherein the distal-most end portion of the treatment member includes a distal tapering portion, a proximal tapering portion, and a ring shaped portion between the distal tapering portion and the proximal tapering portion, the distal tapering portion and the proximal tapering portion including the coating configured to help facilitate the grinding of the substance inside the body lumen. ### Claim 13 (depends on 12) The medical device of claim 12, wherein the ring shaped portion has a constant outer diameter, and the coating on the distal tapering portion and the proximal tapering portion configured to help facilitate the grinding of the substance inside the body lumen is a diamond grind coating. ### Claim 14 (depends on 1) The medical device of claim 1, wherein the at least one window comprises a plurality of circumferentially spaced-apart windows. ### Claim 15 (depends on 1) The medical device of claim 1, further comprising: the aspiration source. ### Claim 16 (depends on 1) The medical device of claim 1, wherein the distal-most end portion of the treatment member includes a distal tapering portion and a ring shaped portion between the distal tapering portion and the intermediate portion; and a taper shape of the distal tapering portion is different from a taper shape of the intermediate portion. ### Claim 17 A medical device, the medical device comprising: an outer tubular member made from one or more rigid materials having a first bend element and a second bend element, the second bend element being proximal to the first bend element in a natural state; a drive shaft and a rotatable treatment member configured to be accommodated in the outer tubular member; the treatment member on a distal end of the drive shaft, the treatment member configured to rotate and grind a substance inside a body lumen by rotating about a central axis, the treatment member including a distal-most end portion, a proximal end portion, and an intermediate portion positioned axially between the distal-most end portion and the proximal end portion, the distal-most end portion, the proximal end portion, and the intermediate portion being configured to be exposed from a distal end of the outer tubular member and to grind the substance inside the body lumen, and wherein the distal-most end portion includes a distally tapering portion and a proximally tapering portion, the proximally tapering portion being proximal of the distally tapering portion, and an intermediate portion of the distal-most end portion located between the distally tapering portion and the proximally tapering portion of the distal-most end portion; and wherein a distal end surface of the treatment member is configured to be directed toward a central axis of a vessel. ### Claim 18 (depends on 17) The medical device of claim 17, wherein the first bend element is configured to redirect the distal end surface of the treatment member away from a wall of the vessel. ### Claim 19 (depends on 17) The medical device of claim 17, wherein a taper shape of the distally tapering portion of the distal-most end portion is different from a taper shape of the proximally tapering portion of the distal-most end portion. ### Claim 20 A medical device, the medical device comprising: an outer tubular member made from one or more rigid materials having a first bend element including a distal end portion of the outer tubular member and a second bend element, the second bend element being proximal to the first bend element in a natural state; a drive shaft configured to be accommodated in the outer tubular member; a rotatable treatment member on a distal end of the drive shaft, the treatment member configured to rotate and grind a substance inside a body lumen, the treatment member including a distal-most end portion, a proximal end portion, and an intermediate portion positioned axially between the distal-most end portion and the proximal end portion, and wherein the distal-most end portion includes a distally tapering portion and a proximally tapering portion proximal of the distally tapering portion, the distally tapering portion tapers toward a distal-most end of the treatment member, the proximally tapering portion tapers toward the proximal end portion, and the intermediate portion tapers toward the distal-most end of the treatment member from a proximal-most end of the intermediate portion to a distal-most end of the intermediate portion; and a bearing between the outer tubular member and the drive shaft, the bearing being positioned distal to the first bend element. ### Claim 21 (depends on 20) The medical device of claim 20, wherein the bearing is a plurality of roller bearings configured to facilitate relative rotation between the treatment member and the outer tubular member. ### Claim 22 (depends on 20) The medical device of claim 20, wherein a taper shape of the distally tapering portion of the distal-most end portion is different from a taper shape of the proximally tapering portion of the distal-most end portion.