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    • 93. 发明申请
    • Surgical repair kit and its method of use
    • 手术修复包及其使用方法
    • US20020193811A1
    • 2002-12-19
    • US10119389
    • 2002-04-09
    • Kwan-Ho Chan
    • A61B017/04
    • A61B17/3403A61B17/0469A61B17/0482A61B17/0483A61B17/062A61B17/3401A61B17/3421A61B2017/00433A61B2017/00526A61B2017/00946A61B2017/06076A61F2/3872
    • A suture passer comprises a longitudinally extending hollow cannula having a central passage slidingly receivable of a surgical suture; a manually graspable handle connected to the hollow cannula for manipulation thereof, the handle having an upper surface; first guide means, connected to the upper surface of the handle, proximate a proximal end of the handle for releasably, guidingly, holding the surgical suture; second guide means, connected to the upper surface of the handle, distal to the first guide means, for releasably, guidingly, holding the surgical suture. The suture passer can be provided in a kit, for use in the suturing of internal tissue, along with a cannula bender, various hollow surgical needles and surgical suture material. The suture passer finds particular use in the suturing of internal tissues which are at least partially accessible through a body cavity, e.g., arthroscopic surgery.
    • 缝合路人器包括纵向延伸的中空套管,其具有滑动地可接收外科缝合线的中心通道; 连接到中空套管的手动抓握手柄用于操纵它,手柄具有上表面; 第一引导装置,连接到手柄的上表面,靠近手柄的近端,用于可释放地,引导地保持手术缝合线; 第二引导装置,其连接到手柄的上表面,远离第一引导装置,用于可释放地,引导地保持手术缝合线。 缝合路人可以设置在套件中,用于缝合内部组织,以及套管弯曲机,各种中空手术针和外科缝合材料。 缝合通道器在缝合内部组织中具有特别的用途,所述内部组织至少部分通过体腔可接近,例如关节镜手术。
    • 95. 发明申请
    • Method and system for mammalian joint resurfacing
    • 哺乳动物关节表面置换的方法和系统
    • US20020173852A1
    • 2002-11-21
    • US10167963
    • 2002-06-12
    • Jeffrey C. FeltMark A. RydellPaul J. BuscemiAlexander ArsenyevChristopher H. Porter
    • A61F002/38
    • A61B17/562A61F2/30721A61F2/34A61F2/38A61F2/3872A61F2/3877A61F2/389A61F2002/30535A61F2250/0058A61L27/18A61L2430/24C08G18/10C08G18/4854C08G18/61C08G18/69C08L75/04C08G18/32
    • A method and system for the creation or modification of the wear surface of orthopedic joints, involving the preparation and use of one or more partially or fully preformed and procured components, adapted for insertion and placement into the body and at the joint site. In a preferred embodiment, component(s) can be partially cured and generally formed ex vivo and further and further formed in vivo at the joint site to enhance conformance and improve long term performance. In another embodiment, a preformed balloon or composite material can be inserted into the joint site and filled with a flowable biomaterial in situ to conform to the joint site. In yet another embodiment, the preformed component(s) can be fully cured and formed ex vivo and optionally further fitted and secured at the joint site. Preformed components can be sufficiently pliant to permit insertion through a minimally invasive portal, yet resilient enough to substantially assume, or tend towards, the desired form in vivo with additional forming there as needed.
    • 一种用于创建或修改整形外科关节磨损表面的方法和系统,涉及准备和使用一种或多种部分或完全预成型和采购的部件,适于插入和放置在身体和关节部位。 在一个优选的实施方案中,组分可以部分固化,并且通常在体外形式离体进一步形成并且在接合部位进一步形成,以增强一致性并改善长期性能。 在另一个实施方案中,预先形成的球囊或复合材料可以插入到关节部位中并且在原位填充可流动的生物材料以符合关节部位。 在另一个实施方案中,预成型组分可以完全固化并离体形成,并任选地进一步装配并固定在接头部位。 预成型组件可以足够柔顺以允许通过微创入口插入,但足够弹性足以基本上假设或倾向于体内所需的形式,并根据需要进一步形成。
    • 98. 发明授权
    • Aldehyde and glycosidase-treated soft and bone tissue xenografts
    • 醛和糖苷酶处理的软骨和骨组织异种移植物
    • US06231608B1
    • 2001-05-15
    • US09248476
    • 1999-02-11
    • Kevin R. Stone
    • Kevin R. Stone
    • A61F228
    • A61L2/10A61F2/08A61F2/28A61F2/30756A61F2/3094A61F2/38A61F2/3872A61F2002/2817A61F2002/2835A61F2002/30677A61L2/0035A61L27/3604A61L27/3608A61L27/3625A61L27/3645A61L27/365A61L27/3687A61L27/3691A61L2430/40
    • The invention provides articles of manufacture comprising substantially non-immunogenic soft and bone tissue xenografts for implantation into humans. The invention further provides methods for preparing soft and bone tissue xenografts by removing at least a portion of a soft or bone tissue from a non-human animal to provide a xenograft; washing the xenograft in saline and alcohol; subjecting the xenograft to cellular disruption treatment; exposing the xenograft to an aldehyde in an amount ranging from about 0.01% to about 0.10%; and digesting the xenograft with a glycosidase and optionally following with a capping treatment. The invention also provides an article of manufacture produced by the above-identified method of the invention. The invention further provides a soft or bone tissue xenograft for implantation into a human including a portion of a soft or bone tissue from a non-human animal, wherein the portion has extracellular components and substantially only dead cells. The extracellular components have substantially no surface carbohydrate moieties which are susceptible to glycosidase digestion. The extracellular components also have an aldehyde in an amount ranging from about 0.01% to about 0.10% crosslinking the proteins of the extracellular components. Each of the xenografts of the invention are substantially non-immunogenic and have substantially the same mechanical properties as a corresponding native soft or bone tissue.
    • 本发明提供包含用于植入人体的基本上非免疫原性的软骨和骨组织异种移植物的制品。 本发明还提供了通过从非人动物中去除至少一部分软组织或骨组织以提供异种移植来制备软骨组织异种移植物的方法; 用盐水和酒精清洗异种移植物; 使异种移植物进行细胞破坏处理; 将异种移植物暴露于约0.01%至约0.10%范围内的醛; 并用糖苷酶消化异种移植物,并任选地进行封端处理。 本发明还提供了通过本发明的上述方法制造的制品。 本发明进一步提供用于植入人的软组织或骨组织异种移植物,其包括来自非人动物的软组织或骨组织的一部分,其中所述部分具有细胞外组分并且基本上仅死细胞。 细胞外组分基本上没有对糖苷酶消化敏感的表面碳水化合物部分。 细胞外组分还具有约0.01%至约0.10%量的醛交联细胞外组分的蛋白质。 本发明的每种异种移植物基本上是非免疫原性的并且具有与相应的天然软骨或骨组织基本相同的机械性质。