Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B17/00—Surgical instruments, devices or methods
  • 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 or setting implements
  • 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
  • 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 or setting implements
  • 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
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B17/00—Surgical instruments, devices or methods
  • 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 or setting implements
  • 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
  • A61B17/8816—Equipment for handling bone cement or other fluid fillers for introducing fluid filler into bone or extracting it characterised by the conduit, e.g. tube, along which fluid flows into the body or by conduit connections

Definitions

• the carrier also includes an inner tube having a first end and a second end, wherein the connector connects the second end of the supply tube with the first end of the inner tube via a chamber such that the supply tube, chamber and inner tube form a lumen having a substantially smooth transition from the supply tube to the inner tube.
• the inner tube is located within the lumen of the elongated portion of the cannula.
• Figure 2 is a cross-section view of the curable material delivery device according to a preferred embodiment of the present invention after insertion of the inner section into the cannula;
• Figure 5 is a cross-section of the connection between the supply tube and the cannula according to a another preferred embodiment of the present invention.
• Figure 8 is a perspective view of the tip portion of the curable material delivery device according to another preferred embodiment of the present invention.
• Figure 9 is a perspective view of the tip portion of the curable material delivery device according to another preferred embodiment of the present invention.
• the distal end 330 of the cannula 30 extends beyond the terminal end 144 of the inner section 140 such that the terminal end 144 of the inner section 140 is at a length from the distal end 330 of the cannula 30 that is less than 50% of the length of the cannula 30.
• the terminal end 144 of the inner section 140 is substantially even with the distal end 330 of the cannula 30.
• an inner section 140 that extends beyond the distal end 330 of the cannula 30 may also be used as long as the inner section 140 fits within the injection site and dispenses curable material effectively.
• the supply section 120 and the inner section 140 are conveniently detachable from each other such that different inner sections 140 may be attached and detached from the supply section 120.
• the inner section 140 comprises an inner section connector 480.
• the inner section connector 480 connects with the cannula connector 130 via the Luer-lock connection 200 that was used to connect to the cannula handle 310 in the previous embodiment.
• the inner section connector 480 also comprises another Luer-lock connection 475 for connection to the cannula handle 310.
• the inner section connector 480 further comprises a second flangeless adapter 420 to provide a precise and smooth transition from the cannula connector 130 to the inner section 140.
• curable material is preloaded to the terminal end 144 of the inner section 140 and the inner section 140 is then inserted into the cannula 30, thus making curable material immediately available to be delivered to the patient.
• curable material need not be preloaded into the carrier assembly to realize other advantages on the present invention.
• the physician may fill two different vertebral bodies in one procedure.
• the technique allows the physician to work between cannulas at various times while keeping the cannulas clean.
• the physician drives cannulas into two or more vertebra.
• the carrier assembly 20 is preloaded with curable material as described above.
• the carrier assembly 20 is connected with the first cannula 30 for the first procedure and curable material is immediately delivered to the vertebra.
• the carrier assembly 20 is removed from the first cannula 30.
• the inner section 140 is still filled with curable material and is thus "preloaded” with respect to the second procedure.
• the carrier assembly 20 is connected to the second cannula 30 and curable material is ready to be immediately delivered to the vertebra.
• the terminal end 144 of the inner section extends beyond the distal end 330 of the cannula 30.
• the tip portion 550 of the terminal end 144 can contain different configurations to deliver curable material to an injection site.
• the tip portion 550 contains a closed, blunt end 518 such that the terminal end 144 is axially closed to the lumen 100 (i.e., material cannot be axially expelled from the terminal end 144 relative to an axis of the lumen 100). That is to say, material in the lumen 100 cannot be forced distally therefrom in an axial fashion.
• the terminal end 100 defines or includes a blunt end 518.
• the blunt end 518 defines a hemispherical surface, although other blunt (i.e., curved or curvilinear) shapes or contours are also acceptable.
• the blunt end 518 is adapted to provide a non-traumatic surface suitable for accessing, contacting and probing bone or tissue while minimizing the risk of puncture and/or coring of the tissue or damage to the bone.

Landscapes

• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Orthopedic Medicine & Surgery (AREA)
• Surgery (AREA)
• Medical Informatics (AREA)
• General Health & Medical Sciences (AREA)
• Biomedical Technology (AREA)
• Heart & Thoracic Surgery (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Molecular Biology (AREA)
• Animal Behavior & Ethology (AREA)
• Engineering & Computer Science (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Physics & Mathematics (AREA)
• Fluid Mechanics (AREA)
• Prostheses (AREA)
• Surgical Instruments (AREA)
• Infusion, Injection, And Reservoir Apparatuses (AREA)

Priority Applications (6)

Applications Claiming Priority (2)

Publications (2)

Family

ID=38429279

Family Applications (1)

Country Status (8)

Families Citing this family (31)

Family Cites Families (18)

• 2006
  • 2006-02-22 US US11/359,184 patent/US7922690B2/en active Active
• 2007
  • 2007-02-22 NZ NZ570585A patent/NZ570585A/en not_active IP Right Cessation
  • 2007-02-22 AU AU2007221229A patent/AU2007221229A1/en not_active Abandoned
  • 2007-02-22 WO PCT/US2007/004758 patent/WO2007100679A2/en not_active Ceased
  • 2007-02-22 EP EP07751514A patent/EP2001399A4/en not_active Withdrawn
  • 2007-02-22 JP JP2008556447A patent/JP2009527334A/ja active Pending
  • 2007-02-22 CA CA2643262A patent/CA2643262C/en active Active
  • 2007-02-22 BR BRPI0708141-3A patent/BRPI0708141A2/pt not_active IP Right Cessation

Non-Patent Citations (1)

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