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    DUAL CAPTURE DEVICE FOR STENT GRAFT DELIVERY SYSTEM AND METHOD FOR CAPTURING A STENT GRAFT
    42.
    发明申请
    DUAL CAPTURE DEVICE FOR STENT GRAFT DELIVERY SYSTEM AND METHOD FOR CAPTURING A STENT GRAFT 有权
    用于椎间盘递送系统的双重捕获装置和用于捕获固定骨架的方法

    公开(公告)号：US20140316510A1

    公开(公告)日：2014-10-23

    申请号：US14300647

    申请日：2014-06-10

    Applicant: Bolton Medical, Inc.

    Inventor： Humberto Berra

    IPC: A61F2/966

    CPC classification number: A61F2/966 ,  A61F2/07 ,  A61F2/86 ,  A61F2/89 ,  A61F2/90 ,  A61F2/915 ,  A61F2/95 ,  A61F2002/075 ,  A61F2002/828 ,  A61F2002/9505 ,  A61F2002/9517 ,  A61F2002/9528 ,  A61F2230/0054

    Abstract: A delivery system for delivering and deploying stents with proximal and distal apices includes a guidewire catheter, a nose cone assembly, a proximal capture portion and a stent graft with proximal and distal stents. The nose cone assembly is at the distal end of the guidewire catheter and includes a nose cone and a distal capture portion. The proximal capture portion is proximal to the distal capture portion of the nose cone assembly. The proximal stent is releasably secured to the distal capture portion and the distal stent is releasably secured to the proximal capture portion. The stent graft can be deployed by releasing the proximal stent and the distal stent from proximal and distal capture portions of the delivery system.

    Abstract translation: 用于递送和展开具有近端和远端顶点的支架的递送系统包括导丝导管，鼻锥组件，近端捕获部分和具有近端和远端支架的支架移植物。 鼻锥组件位于导丝导管的远端，并包括鼻锥体和远端捕获部分。 近端捕获部分靠近鼻锥组件的远端捕获部分。 近端支架可释放地固定到远端捕获部分，并且远侧支架可释放地固定到近侧捕获部分。 可以通过从输送系统的近端和远端捕获部分释放近端支架和远端支架来展开支架移植物。

    TREATMENT METHODS
    43.
    发明申请
    TREATMENT METHODS 审中-公开
    治疗方法

    公开(公告)号：US20140277352A1

    公开(公告)日：2014-09-18

    申请号：US14212693

    申请日：2014-03-14

    Applicant: Colin Gerald Caro ,  Martin G. Burke ,  Paul Gilson ,  Kevin B. Heraty ,  Nicholas Yeo

    Inventor： Colin Gerald Caro ,  Martin G. Burke ,  Paul Gilson ,  Kevin B. Heraty ,  Nicholas Yeo

    IPC: A61F2/82 ,  A61F2/958

    CPC classification number: A61F2/852 ,  A61F2/82 ,  A61F2/915 ,  A61F2/958 ,  A61F2002/068 ,  A61F2002/828 ,  A61F2210/0014 ,  A61F2230/0091

    Abstract: There is disclosed a method of treating hypoxia in tissue of a blood vessel, the method comprising placing a stent in the vessel, the stent having a centre line which curves in three dimensions to promote the supply of oxygen from the blood flowing in the lumen of the stented vessel to the vessel wall. There is disclosed a method of treating a subject with diabetic atherosclerosis, the method comprising placing a stent in a blood vessel of the subject, the stent having a centre line which curves in three dimensions to promote the supply of oxygen from the blood flowing in the lumen of the stented vessel to the vessel wall.

    Abstract translation: 公开了一种治疗血管组织中的缺氧的方法，所述方法包括将支架放置在血管内，所述支架具有三维曲线的中心线，以促进从在内腔中流动的血液中供氧 将支架血管置于血管壁。 公开了一种用糖尿病动脉粥样硬化治疗受试者的方法，所述方法包括将支架置于受试者的血管中，所述支架具有三维曲线的中心线，以促进从在血液中流动的血液中供氧 支架血管的内腔到血管壁。

    Stent System, Deployment Apparatus and Method for Bifurcated Lesion
    44.
    发明申请
    Stent System, Deployment Apparatus and Method for Bifurcated Lesion 审中-公开
    支架系统，分叉病变部位装置及方法

    公开(公告)号：US20140214147A1

    公开(公告)日：2014-07-31

    申请号：US14239611

    申请日：2012-08-20

    Applicant: Khalid Al-Saadon

    Inventor： Khalid Al-Saadon

    IPC: A61F2/954 ,  A61F2/856

    CPC classification number: A61F2/954 ,  A61F2/856 ,  A61F2/958 ,  A61F2002/821 ,  A61F2002/828 ,  A61F2002/91558 ,  A61F2230/006 ,  A61F2230/0069 ,  A61F2250/0007

    Abstract: A deployment apparatus and method for deploying one or more stents to a bifurcated vessel is provided. The invention is particularly suited for T-type bifurcated vessels where a side branch extends from a main branch. The deployment apparatus has a primary inflatable portion for engagement within the main branch and a secondary inflatable portion for engagement within the side branch. A main stent is arranged on the primary inflatable portion and radially expanded within the main branch while the secondary inflatable portion maintains registration with the side branch. A side branch stent is then arranged on the secondary inflatable portion and expanded within the side branch while the primary inflatable portion maintains registration with the expanded main stent. A bifurcated stent system suitable for bifurcated lesions is also provided comprising a side branch stent with a shaped end designed to engage a similarly shaped side opening in a main stent.

    Abstract translation: 提供了用于将一个或多个支架部署到分叉血管的部署装置和方法。 本发明特别适用于侧分支从主分支延伸的T型分叉血管。 展开装置具有用于接合在主分支内的主要可充气部分和用于在侧分支内接合的次充气部分。 主支架布置在主充气部分上并且在主分支内径向扩张，而次充气部分保持与侧分支对准。 然后将侧分支支架设置在次充气部分上并在侧分支内扩张，而主充气部分保持与扩张的主支架对准。 还提供了一种适用于分叉病变的分支支架系统，其包括具有成形端的侧支支架，设计成接合主支架中类似形状的侧开口。

    Intraluminal stent
    45.
    发明授权
    Intraluminal stent 有权
    管腔内支架

    公开(公告)号：US08764815B2

    公开(公告)日：2014-07-01

    申请号：US13780833

    申请日：2013-02-28

    Applicant: Boston Scientific Scimed, Inc.

    Inventor： David Tseng ,  Ellen Golds ,  Bruce A. Parsons

    IPC: A61F2/06

    CPC classification number: A61F2/88 ,  A61F2/90 ,  A61F2002/30322 ,  A61F2002/828 ,  A61F2250/0026 ,  A61F2250/006

    Abstract: An intraluminal stent made of a zig-zag or sinusoidal member defining a successive series of struts connected by apex sections and formed into a series of axially displaced hoop members wherein at least one of the hoop members has at least 5 one strut connected to a strut of an adjacent hoop. The connected struts may be connected by spot welding, continuous welding, or suturing, for example, or by a bridging member connected to each strut, and may be spaced along the length of the stent in a pattern to form a connective spine. The number of zigs of the zig-zag member in each hoop member may be varied, as can the zig length. A plurality of 10 connective spines may also be included.

    Abstract translation: 由锯齿形或正弦构件制成的管腔内支架，其限定由顶端部分连接的连续的一系列支柱，并形成一系列轴向移位的环形构件，其中至少一个环箍构件具有至少5个支柱连接到支柱 的相邻箍。 连接的支柱可以例如通过点焊，连续焊接或缝合连接，或者通过连接到每个支柱的桥接构件连接，并且可以沿着支架的长度以图案间隔开以形成连接脊柱。 每个环形构件中的之字形构件的编弧的数量可以如同Zig长度一样变化。 也可以包括多个10个连接棘。

    STENT FIXATION WITH REDUCED PLASTIC DEFORMATION
    46.
    发明申请
    STENT FIXATION WITH REDUCED PLASTIC DEFORMATION 有权
    具有减少塑性变形的STENT固定

    公开(公告)号：US20140172072A1

    公开(公告)日：2014-06-19

    申请号：US14130213

    申请日：2012-07-02

    Applicant: Alon Shalev

    Inventor： Alon Shalev

    IPC: A61F2/945

    CPC classification number: A61F2/945 ,  A61B2017/00867 ,  A61B2017/1107 ,  A61B2017/1135 ,  A61F2/064 ,  A61F2/852 ,  A61F2002/061 ,  A61F2002/072 ,  A61F2002/828 ,  A61F2250/0039 ,  A61F2250/0063

    Abstract: An endovascular stent system (10) includes first and second generally tubular stents members (20, 22), which are shaped so as to define first and second interface sections (40, 42), respectively, which are securely coupleable to each other. The first interface section (40) is shaped so as to define an opening (44). The second interface section (42) is shaped so as to define a neck portion (50). When the first and second stent members (20, 22) are coupled together, the neck portion (50) is at least in part defined by: (a) first ones (72) of structural elements (70), positioned at respective first circumferential locations, which are configured to apply, to the opening (44), distally- and radially-outwardly-directed forces, without applying any proximally-directed forces, and (b) separate from the first structural elements (72), second ones (74) of the structural elements (70), positioned at respective second circumferential locations different from the first circumferential locations, which are configured to apply, to the opening (44), a proximally- and radially-outwardly-directed forces, without applying any distally-directed forces.

    Abstract translation: 血管内支架系统（10）包括第一和第二大体管状支架构件（20,22），其形状分别限定彼此牢固地连接的第一和第二界面部分（40,42）。 第一界面部分（40）成形为限定开口（44）。 第二接口部分（42）成形为限定颈部（50）。 当第一和第二支架构件（20,22）联接在一起时，颈部（50）至少部分地由以下部分限定：（a）结构元件（70）的第一（72），其位于相应的第一周向 位置，其构造成施加到开口（44），远端和径向向外的力，而不施加任何向近侧方向的力，以及（b）与第一结构元件（72），第二结构元件 所述结构元件（70）的位于不同于所述第一周向位置的相应的第二周向位置处的所述结构元件（70）被配置成向所述开口（44）施加向近侧和径向向外的力，而不施加任何 远程指导力量。

    Mitral Valve Replacement System
    48.
    发明申请
    Mitral Valve Replacement System 审中-公开
    二尖瓣置换系统

    公开(公告)号：US20140142691A1

    公开(公告)日：2014-05-22

    申请号：US14084320

    申请日：2013-11-19

    Applicant: Nakostech SARL

    Inventor： Philippe Pouletty

    IPC: A61F2/24

    CPC classification number: A61F2/2409 ,  A61F2/24 ,  A61F2/2418 ,  A61F2/2427 ,  A61F2/95 ,  A61F2002/828 ,  A61F2220/0008 ,  A61F2220/0025 ,  A61F2230/0054 ,  A61F2250/006

    Abstract: The invention concerns a minimally invasive valve repair system (2), in particular a mitral valve repair system (2) or a tricuspid valve repair system. The system comprises a valve component (3), in particular a mitral valve component (3) or a tricuspid valve component, holding or adapted to hold a valve (4), in particular a mitral valve (4) or a tricuspid valve, respectively. The system (2) comprises a linker-component (6) by means of witch the valve component (3) is linked or linkable to an anchor support (5), in particular an in particular an aortic valve or aortic anchor support (5) or a pulmonic valve or pulmonary artery anchor support, respectively.

    Abstract translation: 本发明涉及微创瓣膜修复系统（2），特别是二尖瓣修复系统（2）或三尖瓣修复系统。 该系统包括分别保持或适于保持阀（4），特别是二尖瓣（4）或三尖瓣的阀组件（3），特别是二尖瓣构件（3）或三尖瓣构件 。 系统（2）包括通过阀部件（3）连接或可连接到锚固支撑件（5），特别是主动脉瓣或主动脉锚固支撑件（5）的接头部件（6） 或肺动脉锚栓支架。

    METHODS OF IMPLANTING A PROSTHESIS
    49.
    发明申请
    METHODS OF IMPLANTING A PROSTHESIS 有权
    植入假体的方法

    公开(公告)号：US20140135896A1

    公开(公告)日：2014-05-15

    申请号：US14105751

    申请日：2013-12-13

    Applicant: Bolton Medical, Inc.

    Inventor： Samuel Arbefeuille ,  Humberto Berra ,  Carol Barbre ,  Michael Moore

    IPC: A61F2/966

    CPC classification number: A61F2/966 ,  A61F2/07 ,  A61F2/89 ,  A61F2/95 ,  A61F2/962 ,  A61F2002/075 ,  A61F2002/828 ,  A61F2002/9505 ,  A61F2002/9511 ,  A61F2002/9517 ,  A61F2002/9528 ,  A61F2002/9665 ,  A61F2210/0014 ,  A61F2230/0091 ,  A61F2250/0098 ,  A61M25/0105 ,  A61M25/0108 ,  Y10T29/49799 ,  Y10T74/18392

    Abstract: A method of implanting a prosthesis in a patient at a treatment site within a blood vessel includes advancing an outer catheter of a prosthesis delivery system in the patient distal to the treatment site, the outer catheter defining an inside diameter and advancing an inner sheath, having greater flexibility than the outer catheter and an outside diameter that is greater than the inside diameter of the outer catheter, and a guidewire lumen of the delivery system from the outer catheter to the treatment site along a guidewire while the outer catheter remains stationary relative to the patient, whereby advancing the inner sheath delivers the prosthesis to the treatment site. The inner sheath is retracted to deploy the prosthesis from within the inner sheath and at the treatment site after which the delivery system from the patient.

    Abstract translation: 将假体植入在血管内的治疗部位的患者体内的方法包括将远端处于治疗部位的患者中的假体输送系统的外导管前进，外导管限定内径并推进内护套，其具有 比外导管更大的灵活性和大于外导管的内径的外径，以及输送系统的导丝管腔，其沿着导丝从外导管到治疗部位，而外导管相对于外导管保持静止 患者，由此前进内鞘将假体递送至治疗部位。 内护套被缩回以从内护套内部和处理部位部署假体，之后从患者输送系统。

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