The present invention relates to interbody implants to be inserted in the intervertebral space defined between two neighbouring vertebrae after intervertebral disk excision, in order to restore the intervertebral space and to form bone fusion between the said neighbouring vertebrae.
More precisely, the domain of the invention is lumbar type interbody implants to restore the height and the angle of the lordosis of the vertebral segment defined by two neighbouring lumbar vertebrae to be mutually secured.
More precisely, the purpose of the invention is an interbody implant, called a secured implant, in other words provided with the means of anchoring the implant in its insertion site, to prevent it from becoming mobile.
There are several stabilised interbody fusion systems for vertebrae known in the state of the art. For example, there is a known stabilised system comprising an interbody implant to be inserted in the intervertebral space defined between two neighbouring lumbar vertebrae. According to one preferred embodiment, this implant is in the form of a cage comprising two sagittal walls connected to each other through an anterior transverse wall and a posterior transverse wall. The walls delimit a volume between them opening up on each side of the transverse faces of the implant. The open volume of the cage will receive a bone filling product called a bone graft, that will come into contact with the vertebral plates to facilitate bone fusion between the two vertebrae.
This type of stabilised system also comprises a stabilising plate extending from the anterior wall of the implant and on each side of the transverse faces. This stabilising plate is provided with passage holes at each of its ends for screws that will be anchored in the vertebrae to be mutually secured.
A stabilising plate can be placed to reliably prevent migration of the implant. However, the applicant has identified a difficulty in keeping the implant in its ideal position within the intervertebral space to enable it to be anchored on the vertebrae to be mutually assembled through the screws. It must be borne in mind that, in different patients, firstly the anterior edges of the plates of the vertebra bodies have different profiles, and secondly implants are located at different distances from the anterior edges of the plates of the vertebra bodies, that causes displacement of the implant while the stabilising plate is anchored on the vertebrae.
The applicant expressed the need to have a stabilised interbody fusion system designed firstly so that the implant can be placed in the intervertebral space in an appropriate position to restore a physiological spinal curvature and lordosis, and secondly to hold the implant in this ideal correction position during anchorage of the stabilising plate on the vertebrae, regardless of the shape of the anterior edges of the plates of the vertebra bodies and the position of the implant relative to these anterior edges of the plates.
Therefore, the purpose of the invention is to satisfy this need by proposing a stabilised interbody fusion system capable of restoring the height and the angle of the lordosis of the vertebral segment by an implant, the function of which is secured by a stabilising plate fixed on the vertebrae.
In order to achieve this objective, the stabilised interbody fusion system for vertebrae according to the invention is of the type comprising:
The stabilised system comprises spacing means interposed between the stabilising plate and the implant, to enable the stabilising plate to be positioned at a specific distance relative to the implant.
Various other special features will become clear from the description given below with reference to the appended drawings that show example embodiments of the purpose of the invention as non-limitative examples.
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As can be seen particularly in
The cage 1 comprises an interior volume 11 delimited by interior vertical faces of the walls 6 to 9 and will be filled by a bone filling product called a bone graft adapted to interbody fusion. This volume 11 opens up on a first transverse face 12 called the upper face in the example illustrated, and a second transverse face 13 called the lower face. These transverse faces 12, 13 are delimited by edges of the walls 6 to 9, preferably arranged to comprise notches 14 enabling the cage to be bonded to the supedjacent and subjacent vertebrae. The notches 14 extend parallel to each other and from a frontal plane F perpendicular to the sagittal plane S and the transverse plane T.
Preferably, the internal volume 11 of the cage comprises one or several connecting walls 15 with other walls. In the example illustrated, the connecting wall 15 is in the general shape of a “Y” and extends between the connecting walls 8 and 9 and the anterior wall 6.
The stabilised interbody fusion system 1 conform with the invention also comprises a stabilising plate 17 for the implant 4. This stabilising plate 17 is provided with at least one passage hole at each of its ends, and in the example illustrated with two passage holes 18 for the screws 19 that will be anchored on vertebrae 2 and 3 to be mutually secured.
According to one preferred characteristic embodiment, the stabilising plate 17 is provided with anti-expulsion means 20 for the anchoring screws 19. These anti-expulsion means 20 are composed of moving flaps installed on the stabilising plate so that they can be guided in rotation in order to occupy a first position in which the passage cross-section of the holes 18 is left free, and a second position in which this passage cross-section is closed off in order to form a stop for the heads of screws 19.
The stabilising plate 17 and the implant 4 are provided with mutual assembly means 21. The stabilising plate 17 is adapted so that after assembly with the implant 4, it extends from each side of the transverse faces 12, 13 to the other, to anchor the screws 19 on the vertebrae 2, 3.
According to one characteristic embodiment, the assembly means 21 consist of an assembly screw 22 that will cooperate with at least one tapped hole 23 formed in the implant 4. For example, a tapped hole 23 is arranged to pass through the anterior wall from one side to the other along an axis perpendicular to the anterior wall 6 and centred on the sagittal plane S of symmetry of the implant 4. Preferably, the implant 4 comprises a series of threaded holes 23 to enable assembly of the stabilising plate 17 in different positions with respect to the implant 4. Thus, a threaded hole 23 is formed in a connecting wall, for example 9, along an axis perpendicular to the axis of the threaded hole 23 formed in the anterior wall 6. At the positions defined by these two threaded holes 23, the stabilising plate 17 is free to occupy two positions perpendicular to each other. Another threaded hole 23 may also be formed in the other connecting wall, 8, at an angle of 45° from the axis of the threaded hole 23 formed in the anterior wall 6.
The assembly screw 22 passes through the stabilising plate 17 through a passage hole 24, bordered by a stop shoulder 25 formed by a dish 26 arranged to hold the head 221 of the assembly screw 22.
According to one characteristic of the invention, the stabilised device 1 comprises spacing means 30 inserted between the stabilising plate 17 and the implant 4, to enable the stabilising plate 17 to be positioned at a specific distance relative to the implant 4. These spacing means 30 fix the stabilising plate 17 onto the vertebrae leaving the implant 4 in its position, taking account of the shape of the anterior edges B of the plates of vertebrae bodies 2, 3 or the setback position of the implant 4 relative to these anterior edges of the vertebrae.
In the example illustrated in
Preferably, the reception part 33 is made by an entry cone cooperating with a complementary part 34 presented by the bushing 31. Cooperation of the bushing 31 with the entry cone 33 is a means of adjusting the distance between the stabilising plate 17 and the implant 4.
The stabilised system 1 according to the invention is used directly as a function of the description given above.
Before the implant 4 is inserted, the disc is excised by preparation of the vertebral plates. The implant 4 is implanted in the intervertebral space 5 between two adjacent vertebrae 2 and 3 to be mutually secured. The implant 4 is designed to restore the height and the angle of the lordosis of the vertebral segment defined by the two neighbouring vertebrae 2, 3. The stabilising plate 17, fitted with its assembly screw 22 provided with its spacer bushing 31, will be installed on the implant 4.
The screw 22 is then screwed into a threaded hole 23 of the implant. The screw 22 is then screwed in until it is fixed in place by the spacer bushing 31 being stopped between the plate 17 and the implant 4. The screws 19 are then anchored in the vertebrae 2, 3.
Obviously, the length of the spacer bushing 31 is adapted to allow the implant 4 to remain in its implantation site, while allowing the stabilising plate 17 to come into contact with the vertebrae. The stabilising plate 17 and the implant 4 are separated by a fixed measurement determined by the spacer bushing 31. Preferably, a range of spacer bushings 31 is available. Each of these spacer bushings 31 has a determined length, each of which is different, to adjust the distance between the implant 4 and the stabilising plate 17.
Note that the implant 4 is preferably provided with at least one radio-opaque element 35 (
According to one example embodiment illustrated in
According to one preferred variant embodiment, each threaded hole 23 of the implant is surrounded by an assembly groove 40, inclined relative to the sagittal plane and designed to cooperate with a gripping or manipulation instrument 44 for use on the implant 4. As can be seen in
According to one preferred variant embodiment, the manoeuvring tube 46 has a curvature and is provided with a slide 50 on which there is a bar 51, the free end of which is adapted to resist forces for placement of the implant and to ensure that the approach is respected.
In the above description, the stabilised interbody fusion system 1 comprises an implant 4 made in the form of a generally parallelepiped shaped cage. Obviously, the purpose of the invention could be used for an interbody implant in the form of a cylindrical or semi-cylindrical cage.
In the above description, the spacer bushing 31 is put into place during assembly of the stabilising plate 17 on the implant 4, while being carried by the assembly screw 22. Obviously, it will be possible for the spacer means 30 to be fixed onto the stabilising plate 17. Similarly,
The invention is not limited to the examples described and illustrated since many modifications can be made without departing from its scope.
| Number | Date | Country | Kind |
|---|---|---|---|
| 0104489 | Apr 2001 | FR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/FR02/01157 | 4/3/2001 | WO |