This invention relates to an intervertebral endoprosthetic device and a method of assembling same and, more particularly, to such a device and method in which a locking mechanism is provided to lock two components of the device.
Spinal discs in the human body may rupture or degenerate to such a degree that the disc has to be surgically removed. In these cases, intervertebral prosthetic devices are available that are designed to be implanted between the adjacent vertebrae to prevent the collapse of the intervertebral space between adjacent vertebrae while maintaining a certain degree of stability and range of pivotal and rotational motion therebetween. Such devices typically include two or more articular elements that are attached to the respective adjacent vertebrae and are adapted to move relative to each other.
Many of these devices, especially those that are inserted in the cervical spine, are either made out of a single component, or are made from multiple components which are permanently fixed together. Therefore, these devices do not offer modularity or revisability without removing the entire assembly.
Although modular systems do exist for use in the lumbar spine, these systems use hinges on the components, or modules, to connect the components. However this type of connection is not robust and/or tends to malfunction, causing disassociation that often results in significant complications.
All patents listed in Table 1 are hereby incorporated by reference herein in their respective entireties. As those of ordinary skill in the art will appreciate readily upon reading the Summary of the Invention, Detailed Description of the Preferred Embodiments and Claims set forth below, many of the devices and methods disclosed in the patents of Table 1 may be modified advantageously by using the teachings of the present invention.
According to an embodiment of the invention, an intervertebral prosthesis is provided that includes an insert that is encapsulated in a base member of the prosthesis in a manner to provide minimal opportunity for disassociation.
Various embodiments of the invention discussed below may possess one or more of the above features and advantages, or provide one or more solutions to the above problems existing in the prior art.
Referring first to
Referring to
The prosthesis 20 is shown in detail in
The lower end plate 26 is also generally rectangular in shape with a curved anterior end surface, and its upper surface includes a generally rectangular recessed area 26a bounded on its two sides and its end by a groove 26b. An access notch 26c is formed in the anterior end portion of the end plate 26 that extends from the outer surface of the end plate to the recessed area 26a, and a ramp 26d is formed at the base of the notch. A tab 26e extends downwardly from the anterior end of the end plate 26. The lower surface of the end plate 26 is flat as shown, but could be contoured to match the corresponding surface of the vertebrae 16 (
It is understood that the end plates 24 and 26 are fastened to the vertebrae 14 and 16, respectively, in any conventional manner which would include locating the tabs 24b and 26e over the corresponding outer anterior surface of the vertebrae 14 and 16, respectively, as shown in
The insert 22 has a domed upper portion 30 formed integrally with, and extending upwardly from, a substantially rectangular lower portion 32. The domed upper portion 30 fits within the recess 24a of the end plate 24 with minimal clearance to form an articulating joint, permitting rotational movement between the insert 22 and the end plate 24.
Two parallel, longitudinally extending, notches 32a and 32b are provided in the rectangular portion 32 and are spaced slightly inwardly from the respective side walls of the rectangular portion. Thus, each portion of the rectangular portion 32 extending between a notch and its corresponding side wall is relatively flexible. A peripheral dovetail projection 32c extends from the side walls and the posterior wall of the rectangular portion 32, and is sized to extend in the corresponding portions of the groove 26b of the end plate 26.
A tab 32d extends outwardly from the anterior end of the insert 22, and has a flat upper surface that is designed to be engaged by a suitable tool. This enables the surgeon to apply a force to the tab 32d in a direction towards the end plate 26 to aid in locking the insert 22 to the lower end plate 26 in a manner to be described.
The insert 22 is attachable to the lower end plate 26 by initially positioning it over the plate at a slight angle to the plane of the latter end plate as shown in
As a result, the insert 22 is locked to the end plate 26 and is substantially encapsulated between the end plates 24 and 26 to considerably reduce the chances for disassociation. Thus, the prosthesis 10 is completed implanted between the vertebrae 14 and 16 as shown in
The insert 22 is modular, and as such, can be revised, or replaced, by another insert of a different size, design, or the like. To this end, the insert 22 can be unlocked from the lower end plate 26 by inserting a proper tool (not shown) through the notch 26c and, using the ramp 26d as a guide, wedging the tool between the lower surface of the rectangular portion 32 of the insert 22 and the upper surface of the end plate 26. The tool can then be pivoted about the ramp 26d to force the insert in a direction away from the end plate 26 to effect the separation. The insert 22 can then be completely disconnected from the end plate 26 by sliding the insert anteriorly relative to the end place 26. This permits the insert 22 to be replaced while maintaining the end plates 24 and 26 in their original positions, secured to the vertebrae 14 and 16.
The embodiment of
The embodiments of
The embodiment of
In all of the above embodiments, the end plates 24 and 26 and may be formed of any suitable biocompatible material including, titanium alloys, cobalt-chrome alloys, stainless steel, alumina, zirconia, polycrystalline diamond, pyrolytic carbon, and the insert 22 can be formed of ultra-high molecular weight polyethylene (UHMWPE), polyetheretherketone (PEEK cross-linked UHMWPE), or other suitable materials. The surfaces of the end plates 24 and 26 and/or the insert 22 may include features or coatings which enhance the purchase or ingrowth qualities of the prosthesis 10. For example, a plazma or biocompatible and osteoconductive material, such as hydroxyapatite (HA), may coat all or a portion of one or more of the above surfaces. Other suitable coatings or treatments may include a porous bead coating, a porous mesh coating, osteogenic peptide coating, growth factor coating, rh-BMP coating, and/or grit blasting. The respective surfaces of the domed portion 30 of the insert 22 and the recessed portion 24a of the upper end plate 24 may be selected or treated to be sufficiently durable to provide acceptable wear characteristics as a result of their articulating movement.
Variations
It is understood that variations may be made in the foregoing without departing from the invention and examples of some variations are as follows:
(1) The prosthesis 10 can be implanted between body portions other than vertebrae.
(2) The prosthesis 10 can be inserted between two vertebrae following a corpectomy in which at least one vertebrae has been removed.
(3) The insert 22 may vary somewhat in shape, size, composition, and physical properties, depending upon the particular area in which the prosthesis is implanted, and more particularly, the space between the end plates 24 and 26 after they have been connected to the vertebrae 14, and 16, respectively.
(4) The upper domed portion of the insert 22 can be replaced by a protrusion of a different shape.
(5) The dome could be formed on the lower surface of the end plate 24 and the corresponding recess formed in the upper surface of the insert 22.
(6) The prosthesis 10 can be implanted between the vertebrae 14 and 16 in a position that is inverted from the position shown in
(7) In the embodiment of
(8) A lug (24c or 26h) can be provided on one of the end plates 24 and 26 and not on the other.
(9) The opening 32d in the embodiment of
(10) The spatial references made above, such as “under”, “over”, “between”, “upper”, “lower”, etc. are for the purpose of illustration only and do not limit the specific orientation or location of the structure described above.
The preceding specific embodiments are illustrative of the practice of the invention. It is to be understood, therefore, that other expedients known to those skilled in the art or disclosed herein, may be employed without departing from the invention or the scope of the appended claims, as detailed above. In the claims, means-plus-function clauses are intended to cover the structures described herein as performing the recited function and not only structural equivalents but also equivalent structures. Thus, although a nail and a screw may not be structural equivalents in that a nail employs a cylindrical surface to secure wooden parts together, whereas a screw employs a helical surface, in the environment of fastening wooden parts a nail and a screw are equivalent structures.