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    ENDOPROSTHESIS
    1.
    发明授权
    ENDOPROSTHESIS 失效
    内置假体

    公开(公告)号：EP0782418B1

    公开(公告)日：1999-12-22

    申请号：EP95930745.5

    申请日：1995-09-14

    申请人： Rogala, Piotr

    发明人： Rogala, Piotr

    IPC分类号： A61F2/32 ,  A61F2/34 ,  A61F2/36

    CPC分类号： A61F2/3603 ,  A61F2/32 ,  A61F2/34 ,  A61F2/38 ,  A61F2/3804 ,  A61F2/40 ,  A61F2/4202 ,  A61F2/4225 ,  A61F2/4241 ,  A61F2/442 ,  A61F2002/30006 ,  A61F2002/30841 ,  A61F2002/30843 ,  A61F2002/30892 ,  A61F2002/3412 ,  A61F2250/0015

    摘要： The implantation method consists in the successive introduction of multilateral needle salients into the spongy bone whilst the needle salients are symmetrically placed on the terminal surfaces of the endoprosthesis, up to the resistance with its edge and the resistance surface, whilst the remaining free area between the needle salients is filled up to the terminal surfaces in the 'biological silence' by osteoblasts. The endoprosthesis distinguishes itself by the fact that it is composed by the glenoid cavity (1) and the head (2) which have round terminal surfaces (3 and 11) with multilateral needle salients (4) which are placed on them (1, 2) with a different length and mutually parallel axes which are perpendicular to the planes in which lies the round resistance edge (6) of the glenoid cavity as well as the resistance plane (10) of the head.

    摘要翻译： 植入方法包括将多边针状突起连续引入海绵状骨中，而针状突起对称地放置在内置假体的末端表面上，直至其边缘和阻力表面抵抗，而其间的自由区域 针状凸起填充到由成骨细胞在“生物沉默”中的终端表面。 内假体的区别在于它由关节盂（1）和头部（2）构成，它们具有圆形终端表面（3和11）以及放置在其上的多边针状凸起（4）（1,2 ）具有不同的长度和相互平行的轴线，所述轴线垂直于关节盂腔的圆形阻力边缘（6）所在的平面以及头部的阻力平面（10）。