US20140188120A1 - Device For Injecting Bone Cement - Google Patents
Device For Injecting Bone Cement Download PDFInfo
- Publication number
- US20140188120A1 US20140188120A1 US14/202,488 US201414202488A US2014188120A1 US 20140188120 A1 US20140188120 A1 US 20140188120A1 US 201414202488 A US201414202488 A US 201414202488A US 2014188120 A1 US2014188120 A1 US 2014188120A1
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- US
- United States
- Prior art keywords
- cannula
- bone cement
- guide wire
- orifice
- radial aperture
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/56—Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
- A61B17/58—Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
- A61B17/88—Osteosynthesis instruments; Methods or means for implanting or extracting internal or external fixation devices
- A61B17/8802—Equipment for handling bone cement or other fluid fillers
- A61B17/8805—Equipment for handling bone cement or other fluid fillers for introducing fluid filler into bone or extracting it
- A61B17/8819—Equipment for handling bone cement or other fluid fillers for introducing fluid filler into bone or extracting it characterised by the introducer proximal part, e.g. cannula handle, or by parts which are inserted inside each other, e.g. stylet and cannula
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/56—Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
- A61B17/58—Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
- A61B17/88—Osteosynthesis instruments; Methods or means for implanting or extracting internal or external fixation devices
- A61B17/8802—Equipment for handling bone cement or other fluid fillers
- A61B17/8805—Equipment for handling bone cement or other fluid fillers for introducing fluid filler into bone or extracting it
- A61B17/8811—Equipment for handling bone cement or other fluid fillers for introducing fluid filler into bone or extracting it characterised by the introducer tip, i.e. the part inserted into or onto the bone
-
- 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
- A61F2/46—Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor
- A61F2/4603—Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor for insertion or extraction of endoprosthetic joints or of accessories thereof
-
- 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
- A61F2/46—Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor
- A61F2002/4677—Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor using a guide wire
Definitions
- the invention relates to a device for injecting bone cement, containing a guide wire and a cannula fitting snugly on the guide wire at least with the inner diameter of its front axial orifice.
- Augmenting osteoporotic bones with injected bone cement for fracture prophylaxis is already known. With the injection cannulae used so far with axial exit aperture, the filling cannot be placed with the desired precision in many cases.
- this object is achieved in that there are closing off means with which the front, axial orifice of the cannula is closable after removal of the guide wire and in that the cannula has a radial aperture, for exit of the bone cement, near the front, axial orifice.
- the closing off means is an inner cannula, closed on its front end, which inner cannula is insertable in the cannula in such a way that its front end closes the orifice of the cannula tightly and has a radial aperture near its front, closed end.
- the diameter of the front, axial orifice of the cannula is smaller than the inner diameter of the cannula and the closing off means is a stopper, the largest diameter of which is larger than the diameter of the front, axial orifice of the cannula.
- the orifice is closed off by the stopper, the entire inner cross-section of the cannula is available for the passage of the bone cement so that in this embodiment the flow resistance for the bone cement is considerably less than with the previously mentioned embodiment.
- this object is achieved in that an inner cannula is provided, closed at its front end, which has near the front, closed end a radial aperture for exit of the bone cement and which fits snugly in the front axial orifice of the cannula at least in a region close to the edge, remote from its front end, of the radial aperture, whereby, after removal of the guide wire, the inner cannula is insertable so far into the cannula that its radial aperture extends beyond the cannula.
- FIGS. 1 a to 1 d show a first embodiment example of a device according to the invention with a cannula with radial aperture and an inner cannula, which likewise has a radial aperture,
- FIGS. 2 a to 2 f show a second embodiment example of a device according to the invention in which the cannula has a radial aperture and is closed in the front by a body, and
- FIGS. 3 a to 3 d show a third embodiment example of a device according to the invention in which the cannula is surpassed in the front by an inner cannula with radial aperture.
- FIGS. 1 a, 2 a and 3 a each show a guide wire 1 which is pointed at its front end 2 .
- This front end 2 of the guide wire is driven forward, under X ray control, into the bone up to some millimeters beyond the place at which the bone cement is supposed to be injected.
- the guide wire typically has a diameter of 2.5 mm and a length of 180 mm; the invention should not be limited, however, to these dimensions.
- a cannula 3 is pushed over the guide wire.
- This cannula 3 has at its front end an orifice 4 with a sharply ground circumferential edge whose inner diameter fits snugly over the guide wire.
- an orifice 4 Disposed on the rear (in the drawing left) end of the cannula is a handle 6 .
- the orifice 4 of the cannula can be slightly reduced and the remaining inner diameter of the cannula can be 3.1 mm, for example.
- the outer diameter of the cannula 3 can be 4 mm, for instance, and its length up to the handle 130 mm.
- a radial aperture 5 Disposed in the cannula near the orifice 4 is a radial aperture 5 , the width of which is somewhat smaller than the inner diameter of the cannula.
- the length of this radial aperture 5 is at least the same as that of the aperture of the inner cannula 9 described further below.
- the handle is of asymmetrical shape, for instance with a pointer-like form the tip of which is aligned with the radial aperture 5 , so that the surgeon knows the angular position of the radial opening 5 at all times.
- the handle 6 has moreover a recess 7 and a coupling 8 , the function of which will be explained further below.
- FIG. 1 c shows the cannula after the guide wire 1 has been pulled out.
- An inner cannula 9 is inserted in the cannula 3 in FIG. 1 d.
- the outer diameter of this inner cannula is 3.0 mm, for instance, so that it can be pushed with play in the cannula 3 .
- the inner diameter of the inner cannula can be 2.5 mm, for example.
- the front end 10 of the inner cannula is closed, and the length of the inner cannula 9 as well as the outer diameter of the end 10 are dimensioned such that, with completely inserted inner cannula 9 , the orifice 4 of the cannula 3 is tightly sealed off.
- a handle 12 Located on the rear end of the inner cannula 9 is a handle 12 , which is also of asymmetrical design, like the handle 6 of the cannula 3 .
- the handle 12 has a protrusion 13 , which forms together with the recess 7 provided on the handle 6 a snap in locking device.
- the inner cannula 9 has a radial aperture 11 in the vicinity of the end 10 , which radial aperture coincides with the aperture 5 of the cannula, with the snap in locking device 7 , 13 in snapped-in state.
- the width of the radial aperture 11 of the inner cannula is somewhat less than its inner diameter, and the length of the aperture 11 is dimensioned in such a way that the exit cross-section of the aperture is at least just as large as the inner cross-section of the inner cannula 9 .
- a coupling 14 provided on the handle 12 serves for attachment of a bone cement source, for instance a needle.
- a bone cement injection with this first embodiment of the device according to the invention runs as follows. First, the guide wire 1 is driven in, as mentioned above. Then the cannula 3 is pushed over the guide wire 1 and pressed in until its radial aperture 5 sits at the place where the injection is supposed to take place. Now the guide wire 1 is pulled out and the inner cannula 9 is inserted in the cannula 3 . After the two handles 6 and 12 are locked together by means of the snap in locking device and a needle with bone cement is connected with the coupling 14 , the injection can begin.
- the physician is able to control the discharge direction of the bone cement into an area-even during the injection by turning the two handles 6 and 12 , locked together, and thus also the two radial apertures 5 and 11 , aligned with one another.
- FIGS. 2 a to 2 f show a second embodiment of the device according to the invention, a guide wire 1 with a tip 2 being shown once again n FIG. 2 a .
- the cannula 3 has in principle the same construction as that in the first embodiment example described above, which is why the same reference numerals have been used here.
- the handle 17 is shaped differently from the handle 7 according to FIGS. 1 b to 1 d, and in particular has no recess 7 because in this second embodiment example there is no inner cannula 9 .
- the orifice 4 of the cannula 3 is closed off with a ball 15 in this embodiment, which ball is pushed into its place with a plunger 16 , as is shown in FIG. 2 d , after pulling back of the guide wire 1 .
- the plunger 16 has a support 18 and is so long that the ball 15 sits at the right place when the support 18 abuts the handle 17 of the cannula 3 .
- the diameter of the ball 15 is slightly smaller than the inner diameter of the cannula 3 , but somewhat larger than the inner diameter of the orifice 4 and also larger than the width of the radial aperture 5 .
- small indentations 19 are provided in the walling of the cannula 3 , as is to be seen in FIG. 2 f .
- the indentations are dimensioned in such a way that during pushing in of the ball 15 a certain resistance must be overcome.
- This second embodiment type of the device according to the invention has the big advantage over the other embodiment types that no inner cannula is necessary and thus the entire inner cross-section of the cannula 3 is available for the flow of the bone cement. This results in a considerably lower pressure loss during injecting.
- FIGS. 3 a to 3 d a guide wire is likewise provided, as can be seen from FIG. 3 a .
- the cannula here has the reference numeral 20 , and differs from the previously described cannulae in that it has no radial aperture.
- the handle 21 of the cannula 20 is also not asymmetrical.
- FIG. 3 c shows an obturator 22 with which the physician makes space outside the orifice 24 of the cannula 20 after the insertion of the cannula 20 in order to then be able to insert the inner cannula 25 , as is shown in FIG. 3 d .
- the obturator 22 has a head 23 and its length is dimensioned such that when the head 23 abuts the handle 21 of the cannula, its front end projects so far out of the orifice 24 as the inner cannula 25 does later.
- the inner cannula 25 has a radial aperture 28 , near its closed end 27 , for exit of the bone cement.
- the inner cannula 25 has a handle 26 which is designed asymmetrically such that the situation of the radial aperture 28 can be seen from its position.
- a bone cement injection runs at the beginning the same way as with both other embodiments in that first the guide wire 1 is driven in and then the cannula 20 is pushed over the guide wire 1 . After removal of the guide wire 1 , the bone tissue is pushed back and compressed with the obturator 22 in the region of the orifice 24 so far that then the inner cannula 25 can be inserted without too much resistance. After insertion of the inner cannula 20 ⁇ sic. 25 >, its radial aperture is aligned as desired through turning of the handle 26 , and the bone cement is injected with a needle connected by means of the coupling 14 .
- All three embodiments described of the device according to the invention thus allow an exact placement of the bone cement filling in that the discharge direction of the bone cement can be determined by turning the respective cannula and can even be changed during the injection.
- both the cannula 3 according to the first embodiment example and the cannula 20 according to the third embodiment example can also be used for axial injection of bone cement, their handles 6 and 21 have a coupling 8 for direct attachment of a needle. The range of cannulae is thereby kept small.
Abstract
Description
- This is a continuation application of U.S. patent application Ser. No. 11/293,289 filed Dec. 1, 2005, which is a divisional of U.S. patent application Ser. No. 10/311,978 filed Dec. 23, 2002, now U.S. Pat. No. 6,997,930 issued Feb. 14, 2006, which is a national phase under 35 U.S.C. §371 of PCT Application No. PCT/CH2000/000355 filed Jun. 30, 2000, the entire contents of each application is incorporated herein by reference.
- The invention relates to a device for injecting bone cement, containing a guide wire and a cannula fitting snugly on the guide wire at least with the inner diameter of its front axial orifice.
- Augmenting osteoporotic bones with injected bone cement for fracture prophylaxis is already known. With the injection cannulae used so far with axial exit aperture, the filling cannot be placed with the desired precision in many cases.
- It is therefore an object of the invention to propose a device for injecting bone cement in which the discharge direction of the bone cement after insertion of the cannula is able to be guided into a particular area.
- According to a first variant of the invention, this object is achieved in that there are closing off means with which the front, axial orifice of the cannula is closable after removal of the guide wire and in that the cannula has a radial aperture, for exit of the bone cement, near the front, axial orifice.
- According to a special embodiment of this variant, the closing off means is an inner cannula, closed on its front end, which inner cannula is insertable in the cannula in such a way that its front end closes the orifice of the cannula tightly and has a radial aperture near its front, closed end.
- According to another, especially preferred embodiment of the first variant, the diameter of the front, axial orifice of the cannula is smaller than the inner diameter of the cannula and the closing off means is a stopper, the largest diameter of which is larger than the diameter of the front, axial orifice of the cannula. When the orifice is closed off by the stopper, the entire inner cross-section of the cannula is available for the passage of the bone cement so that in this embodiment the flow resistance for the bone cement is considerably less than with the previously mentioned embodiment.
- According to a second variant of the invention, this object is achieved in that an inner cannula is provided, closed at its front end, which has near the front, closed end a radial aperture for exit of the bone cement and which fits snugly in the front axial orifice of the cannula at least in a region close to the edge, remote from its front end, of the radial aperture, whereby, after removal of the guide wire, the inner cannula is insertable so far into the cannula that its radial aperture extends beyond the cannula.
- Special embodiments of the invention will be explained in the following, by way of example, with reference to the attached drawings.
-
FIGS. 1 a to 1 d show a first embodiment example of a device according to the invention with a cannula with radial aperture and an inner cannula, which likewise has a radial aperture, -
FIGS. 2 a to 2 f show a second embodiment example of a device according to the invention in which the cannula has a radial aperture and is closed in the front by a body, and -
FIGS. 3 a to 3 d show a third embodiment example of a device according to the invention in which the cannula is surpassed in the front by an inner cannula with radial aperture. -
FIGS. 1 a, 2 a and 3 a each show a guide wire 1 which is pointed at itsfront end 2. Thisfront end 2 of the guide wire is driven forward, under X ray control, into the bone up to some millimeters beyond the place at which the bone cement is supposed to be injected. The guide wire typically has a diameter of 2.5 mm and a length of 180 mm; the invention should not be limited, however, to these dimensions. - According to the embodiment example according to FIGS. la to ld, a cannula 3 is pushed over the guide wire. This cannula 3 has at its front end an
orifice 4 with a sharply ground circumferential edge whose inner diameter fits snugly over the guide wire. By means of this design, bone tissue is prevented from getting into the interior of the cannula 3 during forwards pushing of the cannula 3. Disposed on the rear (in the drawing left) end of the cannula is ahandle 6. Theorifice 4 of the cannula can be slightly reduced and the remaining inner diameter of the cannula can be 3.1 mm, for example. The outer diameter of the cannula 3 can be 4 mm, for instance, and its length up to the handle 130 mm. Disposed in the cannula near theorifice 4 is a radial aperture 5, the width of which is somewhat smaller than the inner diameter of the cannula. The length of this radial aperture 5 is at least the same as that of the aperture of the inner cannula 9 described further below. The handle is of asymmetrical shape, for instance with a pointer-like form the tip of which is aligned with the radial aperture 5, so that the surgeon knows the angular position of the radial opening 5 at all times. Thehandle 6 has moreover arecess 7 and acoupling 8, the function of which will be explained further below.FIG. 1 c shows the cannula after the guide wire 1 has been pulled out. - An inner cannula 9 is inserted in the cannula 3 in
FIG. 1 d. The outer diameter of this inner cannula is 3.0 mm, for instance, so that it can be pushed with play in the cannula 3. The inner diameter of the inner cannula can be 2.5 mm, for example. Thefront end 10 of the inner cannula is closed, and the length of the inner cannula 9 as well as the outer diameter of theend 10 are dimensioned such that, with completely inserted inner cannula 9, theorifice 4 of the cannula 3 is tightly sealed off. Located on the rear end of the inner cannula 9 is ahandle 12, which is also of asymmetrical design, like thehandle 6 of the cannula 3. Thehandle 12 has aprotrusion 13, which forms together with therecess 7 provided on the handle 6 a snap in locking device. Furthermore the inner cannula 9 has a radial aperture 11 in the vicinity of theend 10, which radial aperture coincides with the aperture 5 of the cannula, with the snap inlocking device coupling 14 provided on thehandle 12 serves for attachment of a bone cement source, for instance a needle. - A bone cement injection with this first embodiment of the device according to the invention runs as follows. First, the guide wire 1 is driven in, as mentioned above. Then the cannula 3 is pushed over the guide wire 1 and pressed in until its radial aperture 5 sits at the place where the injection is supposed to take place. Now the guide wire 1 is pulled out and the inner cannula 9 is inserted in the cannula 3. After the two
handles coupling 14, the injection can begin. Thanks to the inventive design of the device, the physician is able to control the discharge direction of the bone cement into an area-even during the injection by turning the twohandles -
FIGS. 2 a to 2 f show a second embodiment of the device according to the invention, a guide wire 1 with atip 2 being shown once again nFIG. 2 a. The cannula 3 has in principle the same construction as that in the first embodiment example described above, which is why the same reference numerals have been used here. One difference is that with the cannula according toFIGS. 2 b to 2 e, thehandle 17 is shaped differently from thehandle 7 according toFIGS. 1 b to 1 d, and in particular has norecess 7 because in this second embodiment example there is no inner cannula 9. Theorifice 4 of the cannula 3 is closed off with aball 15 in this embodiment, which ball is pushed into its place with aplunger 16, as is shown inFIG. 2 d, after pulling back of the guide wire 1. Theplunger 16 has asupport 18 and is so long that theball 15 sits at the right place when thesupport 18 abuts thehandle 17 of the cannula 3. In this embodiment example it is necessary for theorifice 4 of the cannula to be slightly reduced. The diameter of theball 15 is slightly smaller than the inner diameter of the cannula 3, but somewhat larger than the inner diameter of theorifice 4 and also larger than the width of the radial aperture 5. In this way it is ensured that theball 15 can be easily inserted into the cannula 3, but cannot escape through the radial aperture 5 or theorifice 4. So that theball 15 does not roll back in an undesired way after it has been pushed in its place by theplunger 16,small indentations 19 are provided in the walling of the cannula 3, as is to be seen inFIG. 2 f. The indentations are dimensioned in such a way that during pushing in of the ball 15 a certain resistance must be overcome. - This second embodiment type of the device according to the invention has the big advantage over the other embodiment types that no inner cannula is necessary and thus the entire inner cross-section of the cannula 3 is available for the flow of the bone cement. This results in a considerably lower pressure loss during injecting.
- In the third embodiment example illustrated in
FIGS. 3 a to 3 d a guide wire is likewise provided, as can be seen fromFIG. 3 a. The cannula here has thereference numeral 20, and differs from the previously described cannulae in that it has no radial aperture. Thus thehandle 21 of thecannula 20 is also not asymmetrical.FIG. 3 c shows anobturator 22 with which the physician makes space outside theorifice 24 of thecannula 20 after the insertion of thecannula 20 in order to then be able to insert theinner cannula 25, as is shown inFIG. 3 d. Theobturator 22 has ahead 23 and its length is dimensioned such that when thehead 23 abuts thehandle 21 of the cannula, its front end projects so far out of theorifice 24 as theinner cannula 25 does later. Theinner cannula 25 has aradial aperture 28, near itsclosed end 27, for exit of the bone cement. At the other end theinner cannula 25 has ahandle 26 which is designed asymmetrically such that the situation of theradial aperture 28 can be seen from its position. - With this third embodiment of the invention a bone cement injection runs at the beginning the same way as with both other embodiments in that first the guide wire 1 is driven in and then the
cannula 20 is pushed over the guide wire 1. After removal of the guide wire 1, the bone tissue is pushed back and compressed with theobturator 22 in the region of theorifice 24 so far that then theinner cannula 25 can be inserted without too much resistance. After insertion of theinner cannula 20<sic. 25>, its radial aperture is aligned as desired through turning of thehandle 26, and the bone cement is injected with a needle connected by means of thecoupling 14. - All three embodiments described of the device according to the invention thus allow an exact placement of the bone cement filling in that the discharge direction of the bone cement can be determined by turning the respective cannula and can even be changed during the injection.
- So that both the cannula 3 according to the first embodiment example and the
cannula 20 according to the third embodiment example can also be used for axial injection of bone cement, theirhandles coupling 8 for direct attachment of a needle. The range of cannulae is thereby kept small.
Claims (5)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US14/202,488 US20140188120A1 (en) | 2000-06-30 | 2014-03-10 | Device For Injecting Bone Cement |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/CH2000/000355 WO2002002033A1 (en) | 2000-06-30 | 2000-06-30 | Device for injecting bone cement |
US10/311,978 US6997930B1 (en) | 2000-06-30 | 2000-06-30 | Device for injecting bone cement |
US11/293,289 US8702741B2 (en) | 2000-06-30 | 2005-12-01 | Device for injecting bone cement |
US14/202,488 US20140188120A1 (en) | 2000-06-30 | 2014-03-10 | Device For Injecting Bone Cement |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/293,289 Continuation US8702741B2 (en) | 2000-06-30 | 2005-12-01 | Device for injecting bone cement |
Publications (1)
Publication Number | Publication Date |
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US20140188120A1 true US20140188120A1 (en) | 2014-07-03 |
Family
ID=4358098
Family Applications (3)
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US10/311,978 Expired - Lifetime US6997930B1 (en) | 2000-06-30 | 2000-06-30 | Device for injecting bone cement |
US11/293,289 Expired - Lifetime US8702741B2 (en) | 2000-06-30 | 2005-12-01 | Device for injecting bone cement |
US14/202,488 Abandoned US20140188120A1 (en) | 2000-06-30 | 2014-03-10 | Device For Injecting Bone Cement |
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Application Number | Title | Priority Date | Filing Date |
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US10/311,978 Expired - Lifetime US6997930B1 (en) | 2000-06-30 | 2000-06-30 | Device for injecting bone cement |
US11/293,289 Expired - Lifetime US8702741B2 (en) | 2000-06-30 | 2005-12-01 | Device for injecting bone cement |
Country Status (10)
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US (3) | US6997930B1 (en) |
EP (1) | EP1294322B1 (en) |
JP (1) | JP4611607B2 (en) |
AT (1) | ATE288725T1 (en) |
AU (2) | AU2000253847B2 (en) |
BR (1) | BR0017279B1 (en) |
CA (1) | CA2414351C (en) |
DE (1) | DE50009519D1 (en) |
MX (1) | MXPA03000060A (en) |
WO (1) | WO2002002033A1 (en) |
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US20130072941A1 (en) * | 2011-09-16 | 2013-03-21 | Francisca Tan-Malecki | Cement Injector and Cement Injector Connectors, and Bone Cement Injector Assembly |
KR20210011635A (en) * | 2019-07-23 | 2021-02-02 | 오인수 | Bone cement infusion device for percutaneous vertebroplasty |
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- 2000-06-30 CA CA002414351A patent/CA2414351C/en not_active Expired - Lifetime
- 2000-06-30 DE DE50009519T patent/DE50009519D1/en not_active Expired - Lifetime
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- 2000-06-30 AT AT00938436T patent/ATE288725T1/en active
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US20130072941A1 (en) * | 2011-09-16 | 2013-03-21 | Francisca Tan-Malecki | Cement Injector and Cement Injector Connectors, and Bone Cement Injector Assembly |
KR20210011635A (en) * | 2019-07-23 | 2021-02-02 | 오인수 | Bone cement infusion device for percutaneous vertebroplasty |
KR102254320B1 (en) | 2019-07-23 | 2021-06-22 | 오인수 | Bone cement infusion device for percutaneous vertebroplasty |
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CA2414351A1 (en) | 2002-12-24 |
AU2000253847A1 (en) | 2002-04-11 |
BR0017279A (en) | 2003-05-06 |
US20060085008A1 (en) | 2006-04-20 |
AU5384700A (en) | 2002-01-14 |
CA2414351C (en) | 2008-12-09 |
BR0017279B1 (en) | 2013-11-19 |
US8702741B2 (en) | 2014-04-22 |
ATE288725T1 (en) | 2005-02-15 |
DE50009519D1 (en) | 2005-03-17 |
WO2002002033A1 (en) | 2002-01-10 |
EP1294322A1 (en) | 2003-03-26 |
EP1294322B1 (en) | 2005-02-09 |
US6997930B1 (en) | 2006-02-14 |
AU2000253847B2 (en) | 2004-12-16 |
MXPA03000060A (en) | 2004-09-13 |
JP2004501716A (en) | 2004-01-22 |
JP4611607B2 (en) | 2011-01-12 |
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Owner name: DEPUY SYNTHES PRODUCTS, LLC, MASSACHUSETTS Free format text: CHANGE OF NAME;ASSIGNOR:HAND INNOVATIONS LLC;REEL/FRAME:033244/0911 Effective date: 20121231 Owner name: SYNTHES USA, LLC, PENNSYLVANIA Free format text: CHANGE OF NAME;ASSIGNOR:SYNTHES (U.S.A.);REEL/FRAME:033184/0237 Effective date: 20081231 Owner name: HAND INNOVATIONS LLC, FLORIDA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:DEPUY SPINE, LLC;REEL/FRAME:033184/0311 Effective date: 20121230 Owner name: DEPUY SPINE, LLC, MASSACHUSETTS Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:SYNTHES USA, LLC;REEL/FRAME:033184/0272 Effective date: 20121230 Owner name: AUGMENTATION-TECHNOLOGY GMBH, SWITZERLAND Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:JAGGI, KURT;HEINI, PAUL;REEL/FRAME:033184/0165 Effective date: 20021205 Owner name: SYNTHES (U.S.A.), PENNSYLVANIA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:AUGMENTATION-TECHNOLOGY GMBH;REEL/FRAME:033184/0201 Effective date: 20041110 |
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