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公开(公告)号:WO2016149792A8
公开(公告)日:2016-11-24
申请号:PCT/CA2016000079
申请日:2016-03-23
Applicant: JOHNSTON DAVID GERALD
Inventor: JOHNSTON DAVID GERALD
IPC: A61F2/40
CPC classification number: A61F2/40 , A61F2002/30387 , A61F2002/30433 , A61F2002/305 , A61F2002/30578 , A61F2002/4088 , A61F2002/4096
Abstract: A shoulder implant for reestablishing a coracoacromial arch in a subject, the shoulder implant comprising: a dorsal surface substantially shaped as a coracoacromial arch of a shoulder, the dorsal surface for engaging at least a posterior portion of the acromium of the subject when implanted in the subject; and an inferior surface substantially shaped as an acromiohumeral arch of a shoulder, the dorsal surface being opposite the inferior surface. The implant may have a spacer having a convex shape to simulate the anatomic contour of a acromiohumeral arch and the spacer coupled to a baseplate. In certain embodiments, the baseplate and the spacer have a convex surface that may extend the length of the inferior surface of the acromium and anteriorly to the coracoid process.
Abstract translation: 一种肩部植入物,用于在受试者中重新建立冠状凹凸弧,所述肩部植入物包括:背面,其基本上形状为肩部的冠状凸起的拱形,所述背面用于在被植入所述受试者中时与所述受试者的所述肩峰的至少后部接合 学科; 以及基本上形成为肩部的肩峰的下表面,背表面与下表面相对。 植入物可以具有凸起形状的间隔物,以模拟肩胛骨的解剖轮廓和连接到基板的间隔件。 在某些实施例中,底板和间隔件具有凸表面,该凸表面可以延伸母体的下表面的长度并且向前延伸到喙突过程。
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公开(公告)号:WO2016165030A1
公开(公告)日:2016-10-20
申请号:PCT/CH2015/000058
申请日:2015-04-15
Applicant: STARTECH ENGINEERING AG
Inventor: OVERES, Tom , FRIGG, Robert
IPC: A61F2/40
CPC classification number: A61F2/3854 , A61F2/30767 , A61F2/32 , A61F2/40 , A61F2/4014 , A61F2/4081 , A61F2/42 , A61F2002/30028 , A61F2002/30225 , A61F2002/30332 , A61F2002/30364 , A61F2002/30367 , A61F2002/30616 , A61F2002/30635 , A61F2002/30662 , A61F2002/30663 , A61F2002/30932 , A61F2002/30937 , A61F2002/3617 , A61F2002/4018 , A61F2002/4022 , A61F2002/4029 , A61F2002/4085 , A61F2002/4088 , A61F2002/4096
Abstract: An artificial joint implant (1) comprising a first element (2) with a socket (4) and a second element (3) with a ball head (5), wherein said ball head (5) is insertable in said socket (4) such as to form a ball-and- socket connection between said first element (2) and said second element (3), and the movement of said ball head (5) in said socket (4) is restricted by means of a protrusion (6.1; 6.2) engaged in a groove (7), whereby said protrusion (6.1; 6.2) has a central axis A2 and is protruding from the surface of said socket (4) and said groove (7) is provided on the surface of said ball head (5) or vice versa; - said groove (7) is positioned along a great circle of said ball head (5) or of said socket (4), - -said protrusion (6.1; 6.2) has a shape allowing rotation of the protrusion around its central axis A2 when received in the groove (7); and - the surface roughness of the protrusion (6.1; 6.2) and/or of the groove (7) is at most 25 micrometers.
Abstract translation: 一种人造关节植入物(1),包括具有插座(4)的第一元件(2)和具有球头(5)的第二元件(3),其中所述球头(5)可插入所述插座(4) 例如在所述第一元件(2)和所述第二元件(3)之间形成球窝连接,并且所述球头(5)在所述插座(4)中的移动通过突起( 6.1; 6.2),其中所述突起(6.1; 6.2)具有中心轴线A2并且从所述插座(4)的表面突出,并且所述凹槽(7)设置在所述凹槽(7)的表面上, 球头(5),反之亦然; - 所述槽(7)沿着所述球头(5)或所述插座(4)的大圆定位, - 突出部(6.1; 6.2)具有允许所述突起围绕其中心轴线A2旋转的形状, 接收在凹槽(7)中; 和 - 突起(6.1; 6.2)和/或凹槽(7)的表面粗糙度最大为25微米。
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公开(公告)号:WO2016149792A1
公开(公告)日:2016-09-29
申请号:PCT/CA2016/000079
申请日:2016-03-23
Applicant: JOHNSTON, David Gerald
Inventor: JOHNSTON, David Gerald
IPC: A61F2/40
CPC classification number: A61F2/40 , A61F2002/30387 , A61F2002/30433 , A61F2002/305 , A61F2002/30578 , A61F2002/4088 , A61F2002/4096
Abstract: A shoulder implant for reestablishing a coracoacromial arch in a subject, the shoulder implant comprising: a dorsal surface substantially shaped as a coracoacromial arch of a shoulder, the dorsal surface for engaging at least a posterior portion of the acromium of the subject when implanted in the subject; and an inferior surface substantially shaped as an acromiohumeral arch of a shoulder, the dorsal surface being opposite the inferior surface. The implant may have a spacer having a convex shape to simulate the anatomic contour of a acromiohumeral arch arid the spacer coupled to a baseplate. In certain embodiments, the baseplate and the spacer have a convex surface that may extend the length of the inferior surface of the acromium and anteriorly to the coracoid process.
Abstract translation: 一种肩部植入物,用于在受试者中重新建立一个冠状凹凸弧,所述肩部植入物包括:背面,其基本上形成为肩部的冠状凸起的拱形,所述背面用于在被植入所述受试者中时与所述受试者的至少一个后部接合 学科; 以及基本上形成为肩部的肩峰的下表面,背表面与下表面相对。 植入物可以具有凸起形状的间隔物,以模拟肩胛骨的解剖轮廓和连接到基板的间隔件。 在某些实施例中,底板和间隔件具有凸表面,该凸表面可以延伸到肩胛骨的下表面的长度并且在喙突的前方延伸。
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公开(公告)号:WO2015051476A1
公开(公告)日:2015-04-16
申请号:PCT/CH2014/000149
申请日:2014-10-13
Applicant: STARTECH ENGINEERING AG
Inventor: OVERES, Tom , FRIGG, Robert
CPC classification number: A61F2/4014 , A61F2/32 , A61F2/34 , A61F2/36 , A61F2/40 , A61F2/4081 , A61F2002/30028 , A61F2002/30225 , A61F2002/30332 , A61F2002/30364 , A61F2002/30367 , A61F2002/30616 , A61F2002/30635 , A61F2002/30662 , A61F2002/30663 , A61F2002/30932 , A61F2002/30937 , A61F2002/3617 , A61F2002/4018 , A61F2002/4022 , A61F2002/4029 , A61F2002/4085 , A61F2002/4088 , A61F2002/4096 , A61F2230/0093 , A61F2230/0095
Abstract: The present application concerns a shoulder prosthesis assembly (100; 110; 140). The shoulder prosthesis assembly comprises a humeral stem (10) including a first articulating coupling means (14; 43; 81; 130; 160), a base portion (13; 89; 120; 150) of a substantially disc shaped geometry including a second articulating coupling means (17; 46; 86; 127; 153). Said first articulating coupling means (14; 43; 81; 130; 160) and said second articulating coupling means (17; 46; 86; 127; 153) connect the stem (10) to the base portion (13; 89; 120; 150). The ratio between the circumference of the disc shaped base portion (13; 89; 120; 150) and the peripheral thickness of the disc shaped base portion (13; 89; 120; 150) is at least 18:1.
Abstract translation: 本申请涉及一种肩假体组件(100; 110; 140)。 肩假体组件包括肱骨柄(10),其包括第一铰接联接装置(14; 43; 81; 130; 160),基本上圆盘形几何形状的基部(13; 89; 120; 150),包括第二 铰接联接装置(17; 46; 86; 127; 153)。 所述第一铰接联接装置(14; 43; 81; 130; 160)和所述第二铰接联接装置(17; 46; 86; 127; 153)将所述杆(10)连接到所述基部(13; 89; 150)。 圆盘形基部(13; 89; 120; 150)的周长与圆盘形基部(13; 89; 120; 150)的圆周厚度之比至少为18:1。
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公开(公告)号:WO2015051471A1
公开(公告)日:2015-04-16
申请号:PCT/CH2014/000114
申请日:2014-07-24
Applicant: STARTECH ENGINEERING AG
Inventor: OVERES, Tom , FRIGG, Robert
CPC classification number: A61F2/4014 , A61F2/32 , A61F2/34 , A61F2/36 , A61F2/40 , A61F2/4081 , A61F2002/30028 , A61F2002/30225 , A61F2002/30332 , A61F2002/30364 , A61F2002/30367 , A61F2002/30616 , A61F2002/30635 , A61F2002/30662 , A61F2002/30663 , A61F2002/30932 , A61F2002/30937 , A61F2002/3617 , A61F2002/4018 , A61F2002/4022 , A61F2002/4029 , A61F2002/4085 , A61F2002/4088 , A61F2002/4096 , A61F2230/0093 , A61F2230/0095
Abstract: The present application relates to an artificial joint implant (1) comprising a first element (2) with a socket (4) and a second element (3) with a ball head (5). The socket (4) is at least hemispherical and said ball head (5) is inserted in said socket (4) such as to form a ball-and-socket connection between said first element (2) and said second element (3). Movement of said ball head (5) in said socket (4) is restricted in at least one degree of freedom by means of a at least one protrusion (6.1, 6.2) engaged in a at least one groove (7), wherein said at least one protrusion (6.1, 6.2) is provided on said socket (4) and said at least one groove (7) is provided on said ball head (5) or vice versa.
Abstract translation: 本申请涉及一种人造关节植入物(1),其包括具有插座(4)的第一元件(2)和具有球头(5)的第二元件(3)。 插座(4)至少是半球形的,并且所述球头(5)插入所述插座(4)中,以便在所述第一元件(2)和所述第二元件(3)之间形成球窝连接。 所述球头(5)在所述插座(4)中的运动通过至少一个接合在至少一个凹槽(7)中的突起(6.1,6.2)而被限制在至少一个自由度,其中所述 在所述插座(4)上设置有至少一个突起(6.1,6.2),并且所述至少一个凹槽(7)设置在所述球头(5)上,反之亦然。
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公开(公告)号:WO2012037698A1
公开(公告)日:2012-03-29
申请号:PCT/CH2011/000221
申请日:2011-09-20
Applicant: SpineWelding AG , MAYER, Jörg , AESCHLIMANN, Marcel , LEHMANN, Mario , WENGER, Andreas , GOEBEL-MEHL, Stephanie
Inventor: MAYER, Jörg , AESCHLIMANN, Marcel , LEHMANN, Mario , WENGER, Andreas , GOEBEL-MEHL, Stephanie
CPC classification number: A61F2/30 , A61B17/70 , A61F2/30771 , A61F2/30988 , A61F2/4225 , A61F2/4241 , A61F2/4405 , A61F2/442 , A61F2/4425 , A61F2/4611 , A61F2002/30062 , A61F2002/30065 , A61F2002/30067 , A61F2002/30131 , A61F2002/30367 , A61F2002/30469 , A61F2002/30472 , A61F2002/30476 , A61F2002/30563 , A61F2002/30581 , A61F2002/30584 , A61F2002/30604 , A61F2002/30607 , A61F2002/30624 , A61F2002/307 , A61F2002/3082 , A61F2002/30934 , A61F2002/30996 , A61F2002/4092 , A61F2002/4096 , A61F2002/4629 , A61F2002/465 , A61F2002/4681 , A61F2002/4683 , A61F2310/00023
Abstract: A human or animal joint is treated by introduction of a device between the suitably prepared articulating surfaces of the joint, wherein the device is anchored in both these articular surfaces with the aid of a material having thermoplastic properties and with the aid of vibratory energy. For allowing at least limited articulation of the joint after implantation, the device comprises two articulating portions (1 and 2), wherein one of the articulating portions is anchored in each one of the articulating surfaces of the joint. On implantation a proximal face of the device is contacted with a vibrating tool (5) and the vibration is transmitted through parts of the device to locations in which the material having thermoplastic properties is near the bone tissue of the articulating surfaces of the joint and in which liquefaction is desired. The liquefied material penetrates the bone tissue and, on re-solidification forms a positive fit connection between the device and the bone tissue. For achieving targeted and efficient liquefaction and as little energy loss as possible and still allowing articulation of the articulating portions (1 and 2) of the device relative to each other after the implantation, the device is equipped at least for the implantation with a temporal connector portion (4) which connects the two articulating portions (1 and 2) to constitute together with the connector portion (4) and possibly an interface portion (3) a rigid item. The connector portion (4) is removed from the joint immediately after anchoring the articulating portions (1 and 2) or in a second surgical operation after a healing phase in which the joint is immobilized by the connector portion or the connector portion (4) consists of a bio-resorbable or bio-degradable material and is removed gradually by bio-resorption or bio-degradation.
Abstract translation: 通过在适当准备的关节表面之间引入装置来处理人或动物关节,其中借助于具有热塑性的材料并借助于振动能量将装置锚固在这两个关节表面中。 为了允许在植入之后关节至少有限地铰接,该装置包括两个铰接部分(1和2),其中一个铰接部分锚固在接头的每个铰接表面中。 在植入时,装置的近端面与振动工具(5)接触,并且振动通过该装置的部分传递到具有热塑性质的材料靠近关节的关节表面的骨组织的位置 这是需要液化的。 液化物质穿透骨组织,并且在再凝固时,在装置和骨组织之间形成正配合的连接。 为了实现目标和有效的液化和尽可能少的能量损失,并且仍然允许在植入之后相对于彼此铰接部分(1和2)的铰接部分,该装置至少配备有用于植入时间连接器 连接两个铰接部分(1和2)的部分(4)与连接器部分(4)和可能的接合部分(3)一起构成刚性物品。 连接器部分(4)在固定关节部分(1和2)之后立即从关节处移除,或者在通过连接器部分固定关节的愈合阶段之后或第二外科手术中,连接器部分(4)由 的生物可再吸收或生物可降解材料,并通过生物吸收或生物降解逐渐除去。
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