EP2811945A1

EP2811945A1 - Intersomatic implant and tool for installing such an implant

Info

Publication number: EP2811945A1
Application number: EP13706645.2A
Authority: EP
Inventors: Christan BACCELLI; Régis COUEDIC
Original assignee: Implanet SA
Current assignee: Implanet SA
Priority date: 2012-02-08
Filing date: 2013-02-07
Publication date: 2014-12-17
Also published as: US20150012099A1; FR2986416A1; FR2986416B1; US10034761B2; WO2013117861A1

Abstract

The present invention concerns an intersomatic implant (2) comprising a body (4) suitable for being inserted between two vertebrae (1) to space them a predetermined distance apart, the body (4) being provided on either side, respectively, with a contact surface (5, 5') with the corresponding vertebrae (1). The body (4) is formed from an oblong part of predetermined thickness provided at a first so-called proximal end with a gripping cam (9) mounted movable in rotation relative to the part about an axis perpendicular to the two surfaces (5, 5'), between two predetermined angular positions. The contact surfaces (5, 5') are either parallel or substantially parallel to one another, and each contact surface (5, 5') of the body (4) with a corresponding vertebra (1) comprises a set of curved longitudinal protrusions (7, 7', 7'') which decrease in height towards the distal ends thereof.

Description

INTERSOMATIC IMPLANT AND TOOL FOR INSTALLING SUCH IMPLANT

The present invention relates to an intersomatic implant comprising a body adapted to be inserted between two vertebrae to separate them from a determined distance and to put or not in place a bone graft, the body being provided on either side and respectively of a contact face with, or located on the side of a corresponding vertebra.

It also relates to a tool for installing such an implant.

The invention finds a particularly important, although not exclusive, application in the field of spinal surgery and in particular interbody fusion.

Interbody fusion implants are already known for insertion into the intervertebral space defined between two adjacent vertebrae.

Such devices of generally parallelepipedal shape have the disadvantage of imposing an incision of large dimension, that is to say of dimension sufficiently greater than the dimension of the implant in the direction of insertion to allow the introduction and the setting up by the surgeon when he uses the traditional posterior way (on both sides of the thorny).

Implants comprising a pointed end for their insertion and teeth on the upper and lower faces are also known to offer significant resistance to the expulsion of said implant. once it is installed and in all directions.

However, such devices have the disadvantage of allowing only poor control of the positioning of the implants, these being put in place by the joint action of a longitudinal thrust and the friction of the lateral walls of the implant on the periphery of the epiphysis. These devices are therefore neither flexible in terms of positioning of the implant nor adapted for patients with a damaged or weakened epiphysis.

The present invention aims to provide an implant that responds better than those previously known to the requirements of the practice, in particular in that it allows a simple and automatic positioning of the implant with a small incision.

In doing so, an important part of the trauma related to the intervention is avoided, and this in a particularly fragile region, close to the vertebral foramen (spinal cord and root of the nerves).

To do this, she starts with the idea of implanting the transforaminal implant less aggressive for the roots and dura than the posterior approach.

For this purpose, the invention essentially proposes an intersomatic implant comprising a body adapted to be inserted between two vertebrae to remove them from a determined distance and set up a bone graft, the body being provided on either side and respectively of a face of contact with the corresponding vertebra, the body being formed of an oblong piece of said determined thickness provided at a first end said proximal of a cam gripping device rotatably mounted relative to the part about an axis perpendicular to the two faces, between two determined angular positions,

characterized in that the contact faces are parallel or substantially parallel, and in that each contact face of the body with a corresponding vertebra comprises a set of curved longitudinal reliefs, substantially parallel to the side walls, of decreasing height towards their distal ends.

Advantageously, the contact faces are parallel over their entire surface (no beveled corner).

Also advantageously the contact faces are flat between the longitudinal reliefs, that is to say that they form a smooth surface without additional pinion or protrusion to curved longitudinal reliefs.

Such an arrangement will allow the introduction of the body at a certain angle, limiting its size, then the rotation of the body to adopt a final position spacing of the vertebrae by pressing the latter two on either side, of all its area. It is thus possible to introduce it laterally by limiting the size of the incision.

It is also possible to adapt the position of the implant in the vertebra to the pathology to be treated and / or to the physiological conditions of the patient (for example damaged epiphysis, etc.), especially by choosing the optimal distance between the implant and on the one hand the vertebral foramen and on the other hand the dura mater which is made possible by guiding only the upper and lower walls (especially and otherwise smooth) of the implant.

In advantageous embodiments, one and / or the other of the following provisions is also used:

the reliefs consist of ribs;

- the reliefs consist of furrows;

the reliefs consist of an alternation of at least one rib and at least one groove;

reliefs extend over a distance of between 2/5 ^th and 9/10 ^th of the implant curve length and / or are less than 4/5 ^th of the length;

- The reliefs are separated from each other by flat or smooth surfaces, curved, for example of the same width or substantially the same width at the beginning as the reliefs;

the reliefs are in the form of ribs with a continuous upper edge and / or having a decreasing triangular cross-section; the decreasing triangular section decreases by a determined area, for example from 0.5 mm ² to 0 mm ² ;

the piece has two longitudinal side walls connecting the parallel or substantially parallel contact faces of curved shape;

- The cross section of the part parallel to the faces (5, 5 ') of contact is constant and has a bean form.

- The cam is formed by a substantially cylindrical ring pierced from one side of a bore cooperating with a soft friction with a first pin integral with the part forming the axis perpendicular to the two faces;

- The ring has a lateral threaded hole pierced to the bore, for the passage of an instrument to lock or unlock the cam angularly on the axis perpendicular to the body part;

the piece has at its proximal end two parallel cheeks in the extension of the contact faces, open towards the outside, between which the cam is inserted and cooperates with gentle friction;

- The first pin is provided with a side of a passage head in a first cheek and cooperates on the other side with a second screw pin on the first pin through the opposite cheek;

the cam has two locking flats thereof in each of the angular positions determined on the body; the body and the cam are made of titanium or of polymer material.

The invention also provides an insertion tool for the installation of an implant as described above.

To do this, it proposes a tool for inserting an implant as described above, characterized in that it comprises a rod provided with a retractable tip gripper relative to the end of the rod, the surface of this end being of complementary shape to that of the proximal end of the implant, in that the gripping tip is threaded to be screwed into the threaded hole of the ring of the implant, and in that the tool comprises means for retracting the tip inside the rod between a screwing position on the implant and a release position of the implant.

Advantageously, the means for retracting comprise a cylindrical ring rotatable having a spiral guide slot of a pin fixed to an axis integral with the retractable end.

In an advantageous embodiment, the means for retracting comprise a spring arranged to push the retractable end (in the rest position) outside the rod.

The invention will be better understood on reading the following description of embodiments given below by way of non-limiting examples.

The description refers to the accompanying drawings in which: FIG. 1 is a vertebra in plan view on which an implant has been schematically shown according to a first embodiment of the invention.

- Figure 2 is a perspective view of the implant of Figure 1 with the cam in a first position.

FIG. 2A is a dissociated view of the implant of FIG. 2.

FIG. 3 is a perspective view of the implant of FIG. 2 with the cam in a second position.

FIG. 4 shows a sectional view from above of the implant of FIG. 2.

FIG. 5 is a perspective view of another embodiment of the implant according to the invention with orifice for placement of a graft.

FIGS. 6A and 6B illustrate the placement of the implant in the insertion position (FIG. 6A) and then in rotation for final placement (FIG. 6B).

- Figure 7 is a side view of a tool according to one embodiment of the invention.

FIG. 8 is a partial cross-sectional view along VIII-VIII of FIG. 7.

- Figures 9A and 9B show an enlarged view of a retraction ring according to one embodiment of the tool according to the invention before and after retraction.

- Figure 10 is a partial view of the tip of the tool more particularly described. FIG. 1 shows a vertebra 1 seen from above, on which an implant 2 is placed.

The invention can be used with all types of vertebrae including cervical, thoracic, lumbar or pelvic.

Depending on the state of the intervertebral disc 3 between the two vertebrae 1, the implant 2 is inserted inside or next to the disc 3 according to the arrow F.

FIG. 2 shows the implant 2 which is in the form of a body 4 in the form of a small plate of constant thickness having an aspect of oblong shape, provided on both sides and respectively with a contact face 5, 5 'with a corresponding vertebra, namely an upper face 5 and a lower face 5', parallel to each other.

More precisely, the body 4 has a constant longitudinal section parallel to the faces, for example in the form of a bean, defining curved longitudinal walls 6, 6 ', lateral, perpendicular to the faces 5 and 5', the wall 6 having a smaller radius of curvature as the wall 6 '.

This shape allows the implant 2 to bypass the gelatinous portion (not shown) of the intervertebral disc 3 being anchored in the fibrous portion of the disc 3 and to avoid proximity of the nerves of the spine.

At least one face 5, 5 'of contact comprises a set of longitudinal reliefs forming concave ribs or grooves, for example three curved ribs 7, 7 ', 7'', substantially parallel to each other and to said curved side walls 6, 6'.

The reliefs are for example equal at least to 3/5 ^th of the length of the body, hollow (e.g. grooves or groove) or projections (ribs) with respect to the surface, for example with a shaped profile of the "v ".

In the embodiment more particularly described here, the grooves are projecting and of overall decreasing height towards the end intended to penetrate first between the vertebrae (distal end).

The radii of curvature of the curved grooves 7, 7 ', 7 "are for example increasing as they are further from the center of the concavity.

The configuration of grooves 7, 7 ', 7' 'will allow, by friction of the ribs with the surfaces of the vertebrae 1 and / or the intervertebral disc 3, a natural rotation of the implant 2 promoting its automatic positioning.

According to the embodiment more particularly described, the two contact faces 5, 5 'each comprise a play for example of three grooves, games symmetrical to each other with respect to the median transverse plane of the body 4.

Thus when the implant 2 is installed between two vertebrae, the upper face 5 is in contact with the lower face of the upper vertebra, and the lower face 5 'of the implant is in contact with the upper face of the lower vertebra, said faces defining a plate of thickness e determined corresponding to the desired spacing distance and / or the minimum distance between the two superimposed vertebrae.

The thickness e is for example between 6 mm and 18 mm.

The body 4 comprises, at one (8) of its ends, a gripping cam 9 mounted rotatably relative to the body 4 about an axis 9 'perpendicular to the two faces 5, 5' between two defined angular positions .

FIG. 2A shows the disassembled gripper cam 9 and the end 8 of the body 4 to receive the gripping cam 9.

More specifically, a recess formed by two parallel cheeks 10, 10 'in the form of partially circular disks located in the extension of the contact faces 5, 5' is provided for receiving the cam 9, which is inserted therein to cooperate with the said friction pads. play.

Each cheek 10, 10 'comprises a hole 11, 11' passing through its thickness, substantially positioned at its center, the holes being opposite one another, and intended to receive respectively the pins 12 and 13 with whom they collaborate.

Each peg 12, 13 comprises a cylindrical head 14, 14 'of diameter slightly smaller than that of the corresponding hole 11, 11' so as to be able to fit therein while being free to rotate, and a cylindrical body 15, 15 'integral with the corresponding head 14, 14 '. The body 15 is formed of a rod of shorter length than that of the recess between the two cheeks and is arranged to cooperate with the body 15 'itself formed by a small cylinder hollowed by a bore 16' in which the rod 15 is embedded.

After mounting the cam 9 which will be described more precisely below, the two pins 12, 13 are fixed relative to each other for example by gluing or welding.

The gripping cam 9 is formed by a ring

17 substantially cylindrical diameter similar to that of the cheeks 10, 10 'and height arranged to allow free pivoting with a slight friction in the space defined between the cheeks 10, 10'.

The ring 17 is pierced right through by a bore 18 whose inner surfaces cooperate with gentle friction with the outer wall of the cylindrical body 15 'thus forming an axis of rotation of the ring perpendicular to both faces.

In one embodiment, the gripping cam 9 comprises on at least one of its upper faces 19 and / or lower 19 'an outer bore 20, of larger diameter than that of the bore 18, adapted to form a suitable shoulder to collaborate with the head 14, 14 'pawns 12, 13 corresponding.

The gripping cam 9 also has a threaded lateral hole 21 pierced to the bore 18, for the passage of an instrument adapted to block or to unlock the rotation of the cam 9 angularly on the axis formed by the pins.

FIG. 3 shows the implant of FIG. 2 after rotation (arrow f) of the cam 9.

Figure 4 is a sectional top view of the implant 2 showing the gripping cam 9 in the insertion position.

The axis of the lateral threaded hole 21 is then substantially parallel to the (proximal) proximal / distal axis A of the body 4 of the implant 2.

According to the embodiment of the invention more particularly described, the gripping cam 9 further has a lateral wall 22 provided with two flats 23, 24 for locking forming an angle α between them, and connected to each other. by a rounded surface 25 tangent to said flat.

Preferably the angle a is between 60 ° and 100 °, for example 90 °.

During rotation around the axis 9 'of the pins 12, 13 of the cam 9 gripping, each flat 23, 24, in the direction of rotation, will abut with the flat inner portion 26 of the body 4 of the implant, for example perpendicular or substantially perpendicular to the axis A.

The angle a defines the angular range of rotation of the cam 9 by abutment of one then the other of the flats 23, 24.

Figure 5 shows an implant 2 'similar to that previously described with a central recess 27 for graft. In the rest of the description, the same reference numbers have been used to designate identical or similar elements.

More specifically, the body 4 'of the implant 2' has a central portion having a larger width provided with the recess 27, for example of rectangular section, passing through the body from one side.

Advantageously, the angles 28, 28 ', 28' ', 28' '' of this recess 27 are rounded, the latter being substantially centered on the body 4.

Here again, the surfaces 5, 5 'comprise reliefs 7, 7' which are longitudinal and curved in grooves of increasing depth, from the distal end to the proximal end, the grooves 7, 7 'having a profile in the form of "V" and forming a tip at the distal end.

The grooves 7, 7 'have the same properties as those defined with reference to Figure 2 and run from one end to the other of the implant 2, being interrupted by the orifice 27 for example obtained by removal of material .

The orifice 27 makes it possible to insert a graft, that is to say a piece of implantable bone tissue in the human body.

It is understood that the implant 2 may be of any material, biocompatible and preferably adapted to be implanted in the human body, for example titanium or decomposable polymeric material. We will now describe the introduction of an implant 2 according to an embodiment of the invention and the necessary tool for it.

Figures 6A and 6B first show an implant 2 connected to the head 29 of an insertion tool 30 (see Figure 7) respectively at the beginning and end of operation.

The tool 30 is of generally elongate shape, being similar to a screwdriver. It is composed in its most proximal part of a grip handle

31 continued by a locking / unlocking mechanism

32 of the connection of the gripping cam 9 to the tool 30.

It also comprises a mechanism 33 for releasing the rotation of the gripping cam 9 via a rod cylinder 34 provided in its most distal part of the head 29 for connection to the gripping cam 9.

The rod cylinder 34 of relatively long size, for example between 15 and 25 cm, allows in particular to work at a sufficient distance from the incision, to avoid having to arrange a passage of the tools in the body of the patient and / or a significant displacement of the organs forming obstacles, thus minimizing the operating risks and trauma of said organs. It also allows easier thrust of the implant 2 in the disc 3.

FIG. 8 is a diagrammatic sectional view and in more detail the locking / unlocking mechanism 32. The mechanism 32 for blocking / unblocking the connection of the gripping cam 9 is controlled by a serrated head screw 35, arranged to drive in its rotation a locking nut 37 mounted radially on a pressure rod 38.

The pressure rod 38 has at its proximal end a pre-compressed spring 39 and is connected at its distal end to a circular stop 40 which is free to rotate.

The stop 40 is contained in an internal space having dimensions adapted to allow its translation, corresponding to a distance D between 1 and 3 mm.

The abutment 40 is connected on the other side to a rod 41 included in the internal space defined by the rod 34 and opening at the distal end 29 of the tool 30 via a threaded end 42 (FIG. 10).

The rotation of the serrated knob control screw therefore causes rotation of the locking nut 37 which itself causes the rotation of the pressure rod 38 which echoes its movement to the stop 40 which rotates the rod 41 which thus allows the screwing / unscrewing of the tool 30 on the implant 2.

The movable stop 40 is held in its longitudinal position by the pressure rod 38 on which the pre-compressed spring 39 presses.

A knurled ring 43 mounted on a cylinder 44 of threaded translation makes it possible to adjust the counterpressure provided to the stop 40. The translation of the abutment 40 translates in translation translationally the rod 41 and consequently the retractable end 42.

Figure 10 shows schematically an embodiment of the connection tip 29.

The distal end of the tool 30 terminates in an end of the support rod 34 protruding from the protruding end 42 which ends by the thread 45 which can be screwed into the bore of the ring 17.

The rod 34 further comprises at its end a surface 46 with respect to which the retractable end 42 is projecting.

The surface 46 is concave, that is to say of rounded shape towards the inside of the tool 30, of complementary shape to the proximal end of the implant 2.

In the locking / locking position of the rotation the retractable end thereof is in the retracted position in the cylinder, that is to say that the extension of the end 42 retractable relative to the support cylinder is minimal.

In the unlocking / unlocking position of the rotation of the retractable end 42, the latter is in the maximum projecting position.

When the tool 30 is in the locked position, the retractable end 42 taken in the ring 17 of the implant 2 keeps it in contact with the rounded surface 45 of complementary shape, the rounded complementary shape preventing rotation of the the implant 2. During the transition between the locking and unlocking positions, the implant 2 is found away from the rounded surface 46 of complementary shape which no longer blocks the rotation of the implant 2.

FIGS. 9A and 9B show a view of the control of the mechanism 47 for releasing the rotation of the implant 2 of the insertion tool 30 in the locked position and in the unlocked position respectively.

The control is performed by the knurled ring 43 on which is mounted a cylinder 48 comprising a pin 49 projecting radially.

The pin 49 is guided in a chute 50 which runs on the periphery of the cylinder 48, on less than one turn of the cylinder 48.

Thus the pin 49 has two stop positions. A locking position when the knurled ring 43 is in its most proximal position and an unlocking position when the knurled ring 43 is in its most distal position.

We will now describe the implementation of an implant according to the embodiment of the invention more particularly described.

After making an incision and / or removing material from the intervertebral disc 3, the medical practitioner, for example the surgeon, connects the distal end of an insertion tool to the grip cam 9.

This connection is made by the face of a portion of the end of the tool 30 inside the thread of the lateral hole 21 of the ring 17. The connection is made on a low depth of the ring 17 such as for example corresponding to four turns of the end of the tool 30 in the thread.

The low number of turns of face performed allows easier disconnection of the tool 30 without involving spurious rotation of the implant 2 in the direction of rotation of the screw.

The surgeon then presents the distal portion opposite the gripping cam 9 at the incision.

The insertion is facilitated by the relatively small surface of the inserted profile, that is to say the distal end of the implant 2, and the almost zero height at this end of the curved grooves 7, 7 ', 7' .

The surgeon then practices a rectilinear thrust colinear alignment tool 30 / implant 2 following the arrow F (see Figure 6A and 6B).

During this pushing, the friction between the implant 2 and its medium increases in particular because of the grooves 7, 7 ', 7 "and their increasing height as the advance of the implant 2 in the disk 3.

The grooves 7, 7 ', 7 "thus form in the insertion medium.

The radii of curvature of the grooves 7, 7 ', 7' 'then form a guide rail and tend to rotate the implant 2 creating a rotational force.

When the surgeon estimates the position of the implant 2 adequate, it releases the rotation thereof. The release of the rotation is effected by the release of the rotation of the cam 9 gripping.

The cam 9 being free to rotate in a certain angular range, under the effect of the pressure exerted by the surgeon, the implant 2 then performs a rotation having as a center the axis of the cam 9 gripping.

The conformation of the gripping cam 9 and its flats 23, 24 provides the angular freedom range of the implant 2.

Under the combined effect of the oblong shape of the implant 2, grooves 7, 7 ', 7' 'and the degree of freedom in rotation of the cam 9, the implant 2 thus finds its position in the intervertebral disk 3 .

It should then be noted that because of the automatic positioning of the implant 2 and its profile, the initial incision of insertion of the implant 2 can be reduced, thus involving surgical risks and less trauma for the patient.

The oblong profile reduces the insertion surface and therefore the resistance and optimizes the penetration.

In embodiments comprising an inner lateral surface of radius of curvature greater than that of the outer lateral surface, that is to say having a bean shape, the convex nature of the ends of the implant induces resistance to expulsion side of the implant.

Despite the guidance provided by the reliefs and determining the resistance to said expulsion Laterally, the invention has not only excellent resistance to transverse stresses through reliefs but experience shows that a very low rate of displacement / lateral expulsion appears.

As is obvious and as also follows from the above, the present invention is not limited to the embodiments more particularly described. On the contrary, it embraces all variants.

Claims

1. Implant (2) intersomatic comprising a body (4) adapted to be inserted between two vertebrae (1) to remove them from a determined distance and set up a bone graft, the body (4) being provided with both sides and another and respectively a face (5, 5 ') of contact with the corresponding vertebra (1), the body (4) being formed of an oblong piece of said determined thickness provided at a first end said proximal a gripping cam (9) mounted to rotate relative to the workpiece about an axis perpendicular to the two faces (5, 5 '), between two determined angular positions,

characterized in that the contact faces (5, 5 ') are parallel or substantially parallel, and in that each face (5, 5') of contact of the body (4) with a corresponding vertebra (1) comprises a set of longitudinal protrusions (7, 7 ', 7' ') curves, substantially parallel to the side walls (6, 6'), decreasing in height towards their distal ends.

2. Implant according to claim 1, characterized in that the reliefs are separated from each other by smooth surfaces.

3. Implant according to claim 1 to 2, characterized in that the reliefs consist of ribs.

4. Implant according to claim 3, characterized in that the ribs have a continuous upper edge and a decreasing triangular cross section.

5. Implant according to claim 1 to 2, characterized in that the reliefs consist of grooves.

6. Implant according to claim 1 to 2, characterized in that the reliefs consist of an alternation of at least one rib and at least one groove.

7. Implant according to any one of the preceding claims, characterized in that the piece has two longitudinal side walls (6, 6 ') connecting the faces (5, 5') of contact parallel or substantially parallel, of curved shape.

8. Implant according to any one of the preceding claims, characterized in that the cross section of the workpiece parallel to the faces (5, 5 ') of contact is constant and has a bean form.

9. Implant according to any one of the preceding claims, characterized in that the cam (9) is formed by a substantially cylindrical ring (17) pierced from one side of a bore (18) cooperating with a soft friction with a first pin (12) integral with the piece forming the axis perpendicular to both faces (5, 5 ').

10. Implant according to claim 9, characterized in that the ring (17) has a hole (21) threaded laterally pierced to the bore (18), for the passage of an instrument to lock or unlock the cam angularly on the axis perpendicular to the body part 4.

11. Implant according to any one of the preceding claims, characterized in that the present part at its proximal end two cheeks (10, 10 ') parallel in the extension of the faces (5, 5') of contact, open towards the outside, between which the cam (9) is inserted and cooperates with gentle friction.

12. Implant according to claim 11 dependent on the 7, characterized in that the first pin (12) is provided with a side of a head (14) passage in a first cheek (10) and cooperates with the other side with a second pin (13) screwing on the first pin (12) through the cheek (10 ') opposite.

13. Implant according to any one of the preceding claims, characterized in that the cam (9) has two flats (23, 24) for locking thereof in each of the angular positions determined on the body (4).

14. Implant according to any one of the preceding claims, characterized in that the body (4) and the cam (9) are made of titanium or polymer material.

15. Tool (18) for insertion of an implant (2) according to any one of the preceding claims, characterized in that it comprises a rod (32) support comprising a rod (40) gripper, one end (44). ) is projecting from the surface (45) defined by the end (33) of the support rod (32), said surface (45) is a concave surface directed inwardly of the support rod (32), said concave surface (45) being complementary in shape to the proximal end of the implant (2),

in that the end (44) of the gripper shaft (40) is threaded (41), and in that the tool (27) comprises means (30) for rotating the gripper shaft (40) and means (31) for translating said shaft (40) into the support shaft (32).