FR2877833A1 - Prosthesis for correction of lordosis to improve the mobility of the spinal column, comprises titanium rigid plates, incompressible brace, biocompatible silicone intermediate and rigid emergences - Google Patents
Prosthesis for correction of lordosis to improve the mobility of the spinal column, comprises titanium rigid plates, incompressible brace, biocompatible silicone intermediate and rigid emergences Download PDFInfo
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- FR2877833A1 FR2877833A1 FR0412049A FR0412049A FR2877833A1 FR 2877833 A1 FR2877833 A1 FR 2877833A1 FR 0412049 A FR0412049 A FR 0412049A FR 0412049 A FR0412049 A FR 0412049A FR 2877833 A1 FR2877833 A1 FR 2877833A1
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- rigid
- plates
- plate
- emergences
- correction
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- Granted
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- 229920001296 polysiloxane Polymers 0.000 title claims description 12
- 208000007623 Lordosis Diseases 0.000 title claims description 10
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 title claims description 8
- 239000010936 titanium Substances 0.000 title claims description 8
- 229910052719 titanium Inorganic materials 0.000 title claims description 8
- 238000000465 moulding Methods 0.000 claims abstract description 4
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 238000005452 bending Methods 0.000 claims 1
- 239000000463 material Substances 0.000 description 6
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 230000002093 peripheral effect Effects 0.000 description 4
- 229910052786 argon Inorganic materials 0.000 description 2
- 238000003754 machining Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 241001272720 Medialuna californiensis Species 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 201000008482 osteoarthritis Diseases 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/44—Joints for the spine, e.g. vertebrae, spinal discs
- A61F2/442—Intervertebral or spinal discs, e.g. resilient
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2002/30001—Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
- A61F2002/30003—Material related properties of the prosthesis or of a coating on the prosthesis
- A61F2002/30004—Material related properties of the prosthesis or of a coating on the prosthesis the prosthesis being made from materials having different values of a given property at different locations within the same prosthesis
- A61F2002/30014—Material related properties of the prosthesis or of a coating on the prosthesis the prosthesis being made from materials having different values of a given property at different locations within the same prosthesis differing in elasticity, stiffness or compressibility
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2002/30001—Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
- A61F2002/30108—Shapes
- A61F2002/3011—Cross-sections or two-dimensional shapes
- A61F2002/30112—Rounded shapes, e.g. with rounded corners
- A61F2002/30133—Rounded shapes, e.g. with rounded corners kidney-shaped or bean-shaped
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2002/30001—Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
- A61F2002/30316—The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
- A61F2002/30329—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
- A61F2002/30451—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements soldered or brazed or welded
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2002/30001—Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
- A61F2002/30316—The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
- A61F2002/30535—Special structural features of bone or joint prostheses not otherwise provided for
- A61F2002/30563—Special structural features of bone or joint prostheses not otherwise provided for having elastic means or damping means, different from springs, e.g. including an elastomeric core or shock absorbers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/30767—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
- A61F2/30771—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
- A61F2002/30841—Sharp anchoring protrusions for impaction into the bone, e.g. sharp pins, spikes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2220/00—Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2220/0025—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
- A61F2220/0058—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements soldered or brazed or welded
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2230/00—Geometry of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2230/0002—Two-dimensional shapes, e.g. cross-sections
- A61F2230/0004—Rounded shapes, e.g. with rounded corners
- A61F2230/0015—Kidney-shaped, e.g. bean-shaped
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2250/00—Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2250/0014—Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof having different values of a given property or geometrical feature, e.g. mechanical property or material property, at different locations within the same prosthesis
- A61F2250/0018—Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof having different values of a given property or geometrical feature, e.g. mechanical property or material property, at different locations within the same prosthesis differing in elasticity, stiffness or compressibility
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2310/00—Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
- A61F2310/00005—The prosthesis being constructed from a particular material
- A61F2310/00011—Metals or alloys
- A61F2310/00023—Titanium or titanium-based alloys, e.g. Ti-Ni alloys
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Cardiology (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Transplantation (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Prostheses (AREA)
Abstract
Description
La présente invention concerne un dispositif permettant de corrigerThe present invention relates to a device for correcting
intégralement des lordoses sévères. completely severe lordosis.
A ce jour il n'existe aucun moyen efficace pour rectifier intégralement des lordoses sévères. Les fusions ne résolvent pas le problème.On ne peut apporter qu'une amélioration très limitée en soulageant modérément la douleur. Avec l'appui permanent sur l'arrière des vertèbres la lordose s'accentue irrémédiablement, et les articulaires et les épineuses des deux vertèbres adjacentes se rapprochent au point de se toucher. Avec l'arthrose et les rhumatismes les deux vertèbres finissent par se souder. To date, there is no effective way to completely correct severe lordosis. Mergers do not solve the problem. Only a very limited improvement can be achieved by moderately relieving pain. With permanent support on the back of the vertebrae, the lordosis is accentuated irreparably, and the articular and spinal joints of the two adjacent vertebrae approach each other to the point of touching each other. With osteoarthritis and rheumatism the two vertebrae eventually become welded.
Le dispositif de l'invention permet d'éviter tous ces inconvénients. Il est conçu pour rectifier sans risque technique et sans séquelle une lordose sévère. Il permet donc une intervention sur plusieurs vertèbres dans un même temps. Dans bien des cas, il faut intervenir sur les trois dernières. Il réhausse l'arrière des vertèbres très inclinées, compense l'inclinaison de ces vertèbres et redonne au rachis une courbe normale. Il résiste définitivement à l'écrasement tout en laissant une parfaite mobilité à ces vertèbres. L'intervention peut se pratiquer par voie antérieure mais aussi par voie postérieure. Dans les deux cas, de par sa taille et sa forme, la mise en place du dispositif se fera par le côté des vertèbres. On ne touche pas la face antérieure des vertèbres à traiter de manière à éliminer les risques de séquelles. On exclue la récidive d'une lordose traitée par la mise en place du dispositif de l'invention sur une, ou même, sur plusieurs vertèbres. The device of the invention makes it possible to avoid all these drawbacks. It is designed to rectify a severe lordosis without technical risk and without sequelae. It allows an intervention on several vertebrae at the same time. In many cases, we have to intervene on the last three. It raises the back of the very inclined vertebrae, compensates the inclination of these vertebrae and restores the spine a normal curve. It definitely resists crushing while leaving a perfect mobility to these vertebrae. The procedure can be performed anteriorly but also posteriorly. In both cases, because of its size and shape, the device will be placed on the side of the vertebrae. Do not touch the anterior surface of the vertebrae to be treated so as to eliminate the risk of sequelae. The recurrence of a lordosis treated by placing the device of the invention on one or even several vertebrae is excluded.
Le dispositif de l'invention vise essentiellement à rectifier les lordoses en interposant entre deux vertèbres une prothèse destinée à redresser l'arrière très incliné de la vertèbre supérieure dans le but d'empêcher les articulaires et les épineuses des deux vertèbres adjacentes de se rejoindre et d'en supprimer les séquelles qui en découlent. The device of the invention aims essentially to correct the lordosis by interposing between two vertebrae a prosthesis for straightening the very inclined rear of the upper vertebra in order to prevent the articular and thorny of the two adjacent vertebrae to meet and to remove the consequences that follow.
L'invention consiste donc en une prothèse en ce qu'elle comporte une plaque (1) rigide supérieure, une plaque (2) rigide inférieure, une cale (3) dure, un intermédiaire (4) souple, des émergences (5) rigides. The invention therefore consists of a prosthesis in that it comprises an upper rigid plate (1), a lower rigid plate (2), a hard shim (3), a flexible intermediate (4) and rigid emergences (5). .
Les plaques (1 2) rigides: elles ressemblent ii une demi-lune avec une partie périphérique convexe mais avec toutefois la partie périphérique opposée légèrement concave. Elles peuvent être d'épaisseur variable mais de préférence environ 5/lOèmes de millimètre, elles doivent se rapprocher au mieux d'un vrai disque intervertébral tant par la forme de leur contour que par leur dimension. Elles sont en métal de préférence en titane pur, mais peuvent être aussi en d'autres matières rigides compatibles et assemblables au silicone. Elles servent à la fois de gabarit, de guide, de maintien à l'ensemble de la prothèse entre deux vertèbres. Elles peuvent être obtenues au départ d'une tôle ou par usinage dans la masse. Rigid plates (1 2): they look like a half-moon with a convex peripheral part but with the slightly concave opposite peripheral part. They may be of variable thickness but preferably about 5 / 10ths of a millimeter, they must be as close as possible to a true intervertebral disc both in the shape of their contour and in their size. They are preferably of pure titanium metal, but can also be other rigid materials compatible and assembled with silicone. They serve as a template, a guide, to maintain the entire prosthesis between two vertebrae. They can be obtained from a sheet or by machining in the mass.
La cale (3) dure: elle est incompréssible, elle peut êtrede dimensions variables et de formes différentes. Sa hauteur varie et détermine l'espace souhaité sur l'arrière de la prothèse en fonction de l'angle d'inclinaison de la lordose à corriger. Elle maintient l'arrière de la vertèbre relevé. Elle est en métal de préférence en titane pur, mais peut être en d'autres matières dures compatibles et assemblables à la plaque (1) ou aux deux plaques (1-2) selon le cas. Elle est positionnée à l'arrière de la plaque (1) supérieure juxtaposée sur sa face interne et perpendiculaire à sa surface. Elle est située au centre de la partie concave de cette plaque, parallèle et dans le prolongement de sa surface périphérique, elle en est solidaire et descend au contact de la plaque (2) pour s'y appuyer dessus. Elle a pour fonction d'empêcher l'écrasement de la prothèse sur l'arrière et maintenir l'espace désiré entre les deux plaques (1-2). Elle peut être un parallélépipède usiné avec la plaque (1) en une masse et matière ou un parallélépipède rapporté pour être soudé à sa base supérieure contre la face interne de la plaque (1) au moyen d'une soudure au laser ou d'une soudure à l'argon. Les trois arrêtes intérieures de la base inférieure prenant appui sur la plaque inférieure sont arrondies pour permettre aux mouvements une courbe harmonieuse. Elle peut avoir approximativement à titre non limitatif des dimensions de l'ordre de 5 mm d'épaisseur 10 mm en largeur et 8 mm en hauteur. Elle peut être aussi une portion d'ovale horizontal avec deux faces aplanies et parallèles d'où ne subsiste que la moitié inférieure usinée avec la plaque (1) en une masse et matière ou une portion d'ovale rapportée pour être soudée à sa base supérieure droite contre la face interne de la plaque (1) au moyen d'une soudure au laser ou d'une soudure à l'argon. La partie inférieure ovale vient s'appuyer sur la plaque (2) inférieure. L'ovale permet aux mouvements une courbe harmonieuse. Le diamètre de l'ovale représente environ 30 % de la partie concave de la prothèse. Elle peut être aussi réalisée à partir d'un développé de la plaque (1). Ce développé de longueur correspondante à la hauteur nécessaire est cambré et plié vers l'intérieur de ladite plaque perpendiculairement à sa surface mis en forme avec la base inférieure recourbée et légèrement arrondie. On plie sur une largeur d'environ 10 mm une hauteur d'environ 8 mm, le retour arrondi de la base d'environ 2 mm. Ces dimensions sont non limital:ives. Avec une autre technologie, on peut l'obtenir avec un noyau dur en silicone bio-compatible de forme semi-circulaire avec la partie arrière légèrement concave de manière à suivre la courbe des plaques (1-2) entre lesquelles il est inséré. Le diamètre du noyau dur représente environ 30 % de la périphérie concave de la prothèse. N'ayant pas une couleur spécifique, il ne se distigue pas du reste de l'intermédiaire. L'assemblage du titane et du silicone consiste dans le cas présent en ce qu'on appelle un flash, ce qui implique la nécessité de mouler toute la partie intermédaire en même temps dans un ordre chronologique. On monte les plaques (1-2) en titane à une température de 1000 , on moule le noyau dur entre les deux plaques en compressant à 75 shores le silicone 4770 chauffé à près de 400 . A la suite immédiate, on moule la totalité restante en compressant à 60 shores le silicone 4755 chauffé à près de 400 lui aussi. La dilatation du titane provoquée par la haute température, permet au silicone fluidifié également par sa haute température de s'imprégner superficiellement dans le titane. Il se produit un phénomène d'interpénétration superficielle qui exclue tous risques de séparation des deux matériaux. On refroidit rapidement car l'opération ne peut durer plus de deux minutes. Une fois refroidi, le silicone 4770 compressé à 75 shores devient très dur et presque incompréssible. The wedge (3) lasts: it is incomprehensible, it can be of variable dimensions and of different forms. Its height varies and determines the desired space on the back of the prosthesis according to the angle of inclination of the lordosis to be corrected. It keeps the back of the vertebra raised. It is made of metal preferably of pure titanium, but may be other hard materials compatible and assembled to the plate (1) or to the two plates (1-2) as appropriate. It is positioned at the rear of the upper plate (1) juxtaposed on its inner face and perpendicular to its surface. It is located in the center of the concave part of this plate, parallel and in the extension of its peripheral surface, it is integral and descends in contact with the plate (2) to rely on it. Its function is to prevent crushing of the prosthesis on the back and maintain the desired space between the two plates (1-2). It can be a parallelepiped machined with the plate (1) in a mass and material or a parallelepiped reported to be welded to its upper base against the inner face of the plate (1) by means of a laser weld or a argon welding. The three inner edges of the lower base bearing on the lower plate are rounded to allow the movements a harmonious curve. It may have approximately non-limiting dimensions of the order of 5 mm thick 10 mm wide and 8 mm in height. It may also be a portion of horizontal oval with two flattened and parallel faces from which only the lower half machined with the plate (1) remains in a mass and material or an oval portion added to be welded to its base upper right against the inner face of the plate (1) by means of a laser weld or an argon weld. The oval lower part is supported on the lower plate (2). The oval allows the movements a harmonious curve. The diameter of the oval represents about 30% of the concave portion of the prosthesis. It can also be made from a developed plate (1). This developed length corresponding to the necessary height is arched and folded inward of said plate perpendicular to its shaped surface with the curved lower base and slightly rounded. A height of approximately 8 mm is folded over a width of approximately 10 mm, the rounded return of the base approximately 2 mm. These dimensions are nonlimital: ives. With another technology, it can be obtained with a biocompatible silicone hard core of semi-circular shape with the slightly concave rear part so as to follow the curve of the plates (1-2) between which it is inserted. The diameter of the hard core is about 30% of the concave periphery of the prosthesis. Not having a specific color, he does not disagree with the rest of the intermediary. The assembly of titanium and silicone consists in this case in what is called a flash, which implies the need to mold the entire intermediate part at the same time in a chronological order. Titanium plates (1-2) are mounted at a temperature of 1000, the hard core is molded between the two plates by compressing the 4770 silicone heated to about 400 at 75 bar. Immediately afterwards, the remaining total is molded by compressing to 60 shores the 4755 silicone heated to nearly 400 also. The expansion of titanium caused by the high temperature, allows the fluidized silicone also by its high temperature to impregnate superficially in the titanium. A phenomenon of superficial interpenetration occurs which excludes all risks of separation of the two materials. It cools quickly because the operation can not last more than two minutes. Once cooled, the 4770 silicone compressed to 75 shores becomes very hard and almost incomprehensible.
L'intermédiaire (4) souple est compressible et élastique pour permettre la mobilité des vertèbres traitées. Il est disposé entre les deux plaques (1-2), il occupe entièrement le volume intérieur restant déterminé par la surface des dites plaques et la hauteur de la cale. La surface de sa périphérie est le prolongement de la surface périphérique des dites plaques. L'ensemble plaques et intermédiaire n'est pas obligatoirement parallèle. L'arrière peut être plus épais que le devant en fonction de l'angle d'inclinaison de la lordose à rattraper et déterminé par la hauteur de la cale. Il est obtenu par le moulage du silicone 4755 qui reste compressible et élastique après refroidissement. The flexible intermediate (4) is compressible and elastic to allow the mobility of the treated vertebrae. It is arranged between the two plates (1-2), it occupies entirely the remaining internal volume determined by the surface of said plates and the height of the shim. The surface of its periphery is an extension of the peripheral surface of said plates. The plate and intermediate assembly is not necessarily parallel. The back may be thicker than the front depending on the angle of inclination of the lordosis to catch up and determined by the height of the hold. It is obtained by molding silicone 4755 which remains compressible and elastic after cooling.
Les silicones cités sont fabriqués par les laboratoires NUSIL et référencés: type A. MED 4770 et type A. MED 4755. Ils sont biocompatibles implantables à long terme. The silicones mentioned are manufactured by the laboratories NUSIL and referenced: type A. MED 4770 and type A. MED 4755. They are biocompatible implantable long-term.
Les émergences (5) apparaissent sur la surface de la face extérieure de chaque plaque perpendiculaires à sa surface. Elles peuvent être de forme conique ou pyramidale, d'autres formes sont possibles. Ces émergences sont prévues pour servir d'encrage entre les deux vertèbres à l'ensemble de la prothèse. Elles sont obtenues par emboutissage des plaques (1-2) ou par usinage dans la masse. Elles offrent un double intérêt en étant convexes sur la face externe de ces plaques pour servir d'encrage contre l'os et concaves sur la face interne de ces mêmes plaques pour permettre au silicone de s'imprégner dans les cavités, ajoutant ainsi une sécurité supplémentaire à l'efficacité et à la fiabilité de la tehcnique d'assemblage des deux matériaux. The emergences (5) appear on the surface of the outer face of each plate perpendicular to its surface. They can be conical or pyramidal, other forms are possible. These emergences are intended to serve as inking between the two vertebrae to the entire prosthesis. They are obtained by stamping the plates (1-2) or by machining in the mass. They offer a double interest by being convex on the outer face of these plates to serve as inking against the bone and concave on the inner face of these plates to allow the silicone to soak in the cavities, thus adding security additional to the efficiency and reliability of the assembly technique of the two materials.
Il est entendu que des modifications de l'invention décrite ci-dessus sont couvertes par les revendications annexées. 20 It is understood that modifications of the invention described above are covered by the appended claims. 20
Les dessins annexés illustrent les différents modes de réalisations décrits ci-desus. The accompanying drawings illustrate the various embodiments described above.
La figure (1) est une vue en perspective de la prothèse munie de la cale parallèlépipédique. Figure (1) is a perspective view of the prosthesis provided with the parallelepipedal wedge.
La figure (2) est une vue de coupe de la prothèse munie de la cale parallélépipédique mise en place entre deux vertèbres. Figure (2) is a sectional view of the prosthesis provided with the parallelepiped wedge placed between two vertebrae.
La figure (3) est une vue en perspective de la prothèse munie de la cale ovale. Figure (3) is a perspective view of the prosthesis provided with the oval wedge.
La figure (4) est une vue de coupe de la prothèse munie de la cale ovale mise en place entre deux vertèbres. Figure (4) is a sectional view of the prosthesis provided with the oval wedge placed between two vertebrae.
La figure (5) est une vue de la plaque (1) avant pliage. Figure (5) is a view of the plate (1) before folding.
La figure (6) est une vue de coupe de la prothèse munie de la cale pliée mise en place entre deux vertèbres. Figure (6) is a sectional view of the prosthesis provided with the folded wedge placed between two vertebrae.
La figure (7) représente le noyau dur par transparence. Figure (7) shows the hard core by transparency.
Claims (6)
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FR0412049A FR2877833B1 (en) | 2004-11-15 | 2004-11-15 | CORRECTEUR OF LORDOSES |
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FR0412049A FR2877833B1 (en) | 2004-11-15 | 2004-11-15 | CORRECTEUR OF LORDOSES |
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WO2009071044A1 (en) * | 2007-12-04 | 2009-06-11 | Global Medical Consulting Gmbh | Intervertebral disk prosthesis |
EP2120799A1 (en) * | 2007-03-14 | 2009-11-25 | Synthes GmbH | Intervertebral implant component with three points of contact |
US9717511B2 (en) | 2006-07-31 | 2017-08-01 | DePuy Synthes Products, Inc. | Drilling/milling guide and keel cut preparation system |
US10182831B2 (en) | 2003-04-28 | 2019-01-22 | Centinel Spine Llc | Instruments and method for preparing an intervertebral space for receiving an artificial disc implant |
Families Citing this family (1)
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US8172902B2 (en) | 2008-07-17 | 2012-05-08 | Spinemedica, Llc | Spinal interbody spacers |
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WO1994004100A1 (en) * | 1992-08-24 | 1994-03-03 | Societe De Fabrication De Materiel Orthopedique - Sofamor | Intervertebral disk prosthesis |
WO2001062190A1 (en) * | 2000-02-24 | 2001-08-30 | Stryker Spine Sa | Intervertebral implant with rigid body and support surfaces |
WO2003094806A1 (en) * | 2002-05-10 | 2003-11-20 | Ferree Bret A | Prosthetic components with cushioning elements |
WO2004087021A1 (en) * | 2003-04-03 | 2004-10-14 | Enztec Limited | Load bearing intervertebral disk |
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WO1994004100A1 (en) * | 1992-08-24 | 1994-03-03 | Societe De Fabrication De Materiel Orthopedique - Sofamor | Intervertebral disk prosthesis |
WO2001062190A1 (en) * | 2000-02-24 | 2001-08-30 | Stryker Spine Sa | Intervertebral implant with rigid body and support surfaces |
WO2003094806A1 (en) * | 2002-05-10 | 2003-11-20 | Ferree Bret A | Prosthetic components with cushioning elements |
WO2004087021A1 (en) * | 2003-04-03 | 2004-10-14 | Enztec Limited | Load bearing intervertebral disk |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10182831B2 (en) | 2003-04-28 | 2019-01-22 | Centinel Spine Llc | Instruments and method for preparing an intervertebral space for receiving an artificial disc implant |
US9717511B2 (en) | 2006-07-31 | 2017-08-01 | DePuy Synthes Products, Inc. | Drilling/milling guide and keel cut preparation system |
US9949746B2 (en) | 2006-07-31 | 2018-04-24 | Centinel Spine Llc | Drilling/milling guide and keel cut preparation system |
EP2120799A1 (en) * | 2007-03-14 | 2009-11-25 | Synthes GmbH | Intervertebral implant component with three points of contact |
EP2120799A4 (en) * | 2007-03-14 | 2012-12-19 | Synthes Gmbh | Intervertebral implant component with three points of contact |
WO2009071044A1 (en) * | 2007-12-04 | 2009-06-11 | Global Medical Consulting Gmbh | Intervertebral disk prosthesis |
US8764834B2 (en) | 2007-12-04 | 2014-07-01 | Global Medical Consulting Gmbh | Intervertebral disk prosthesis |
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