A surgical injection device includes at least one tubular element defining a passageway. The passageway is configured for disposal of a selected volume of an agent and an evacuator disposed within the passageway. An actuator is engageable with the evacuator to entirely expel the selected volume of the agent from the passageway to a selected site. Spinal constructs, implants, systems and methods are disclosed.

An apparatus and method for mixing and dispensing bone cement is provided. The apparatus includes a mixing vessel for mixing bone cement attached to a syringe body. The syringe body having a lumen that is connected to the mixing vessel by a passageway between the mixing vessel and the lumen of the syringe body. A separator is provided between the mixing vessel and the syringe body and includes an orifice therein so that when the opening in the separator is misaligned with the lumen the passageway is blocked and when aligned the passageway is continuous with the lumen so that bone cement can pass into the syringe body. A plunger is provided and is slideably movable along the longitudinal axis of the syringe body so as to advance the bone cement out of the distal end of the syringe.

A storage and mixing system, for pasty two-component polymethyl methacrylate bone cements, comprises a cartridge with a cylindrical interior, a cartridge head that closes an end of said cartridge, a partition wall axially disposed in the cylindrical interior of the cartridge, wherein said partition wall is connected to the circumferential surface of the cylindrical interior of the cartridge and divides the cylindrical interior of the cartridge delimited by the cartridge head into two spatially separate cavities. The first cavity includes a first pasty cement component and the separate second cavity includes a second pasty cement component, two delivery plungers close the two cavities on the side of the cavities opposite the cartridge head. At least two cutting edges are disposed on the front side of the sleeve-shaped connecting means facing the cartridge head, such that the at least two cutting edges cut off the partition wall from the cylindrical inner wall of the cartridge as at least one cut-off strip when the delivery plungers are advanced towards the cartridge head in the cavities with the connecting means, and wherein the sleeve-shaped connecting means comprises a deflecting surface which is inclined to the axis of the connecting means which, on advancing the connecting means, presses the at least one cut-off strip of the partition wall towards the inner wall of the cartridge.

A storage and mixing system for pasty two-component polymethyl methacrylate bone cements comprises a tubular cartridge with a cylindrical interior, a cartridge head that closes one end of the tubular cartridge, a partition wall axially disposed in the cylindrical interior and dividing the cylindrical interior into two spatially separate cavities, the first cavity including a first pasty cement component and the second cavity including a second pasty cement component, two delivery plungers disposed movably in the two cavities and connected via a connecting means, wherein a wedge or cone having a cutting edge on the front side thereof facing the cartridge head is disposed on the connecting means, such that said cutting edge cuts open the partition wall when the delivery pistons are advanced towards the cartridge head and the wedge or cone presses the cut open parts of the partition wall towards the inner wall of the cartridge.

A storage and mixing system for pasty two-component polymethyl methacrylate bone cements comprises a tubular cartridge having a cylindrical inner chamber, a dispensing plunger that is axially displaceable in the inner chamber of the cartridge, a partition disposed axially in the tubular cartridge, and a cartridge head which closes one end of the tubular cartridge. The cartridge head has a slot-shaped opening, wherein the partition protrudes from the inner chamber of the cartridge through the slot-shaped opening of the cartridge head, wherein the partition divides the cylindrical inner chamber of the cartridge bounded by the dispensing plunger and the cartridge head into two cavities that are spatially separated from one another. A first pasty cement component is present in the first cavity and a second pasty cement component is present in the separate second cavity, wherein the partition is removable through the slot-shaped opening of the cartridge head so that the two separate cavities are connected to one another after the partition is removed.

The bone cement injection device includes an injection assembly and a filler assembly. The injection assembly includes a barrel, first needle member, second needle member, and plunger. The first needle member is movably housed inside the barrel, and includes a first member body, a first conduit, a side tube, and puller elements. The second needle member is housed in the first needle member, and includes a second member body, and a second conduit. A space is maintained between the first and second conduits. The plunger is joined to the first member body and is movably housed in the second member body. The filler assembly fills bone cement into the second member body. The first needle member is pulled backward, and the plunger injects the bone cement into the patient's bone. With an air compressor connected to the side tube, a negative pressure is created to facilitate bone cement injection.

Various embodiments are described herein for a device for storing first and second ingredient materials, mixing the ingredient materials to form an adhesive material and dispensing the adhesive material. Various embodiments are also described herein for a method of making the device and a method of using the device.

The invention provides a bone cement mixing assembly including a mixer, a syringe barrel and a movable plug cover. The mixer includes a stirring rod and a stirring barrel. The stirring rod has holding end, a rod body and a stirring end. The stirring barrel has a barrel cover, a first barrel open, a first barrel body, a first barrel bottom, and a stirring space located in the first barrel body. The syringe barrel has a second barrel open, a second barrel body, a second barrel bottom, and an injection space located in the second barrel body. In this way, the complete-stirred bone cement in the stirring barrel can be directly collected and pushed into the syringe barrel through the movement of the movable plug cover to achieve the effect of completing the preparation of the bone cement quickly and efficiently.

A method for treating arthritis of a joint includes identifying a bone lesion in a bone adjacent to the joint; and implanting in the bone a reinforcing member in or adjacent to the bone lesion. A kit for conducting the method includes: (a) at least one reinforcing member having a proximal face adapted to face the joint, a distal face adapted to face away from the joint, and a wedge-shaped edge adapted to pierce bone, wherein the at least one reinforcing member is planar and sterile; and (b) a container adapted to maintain the at least one reinforcing member sterile. Another kit includes: (a) a sterile fluid; (b) a syringe for injecting the fluid into a bone; (c) a curing agent adapted to cure the fluid to polymerize and/or cross-link; and (d) a container adapted to maintain the sterility of contents of the container.

A femoral component kit includes a piston. The piston includes a notch formed in a bottom surface. The kit includes a femoral component mold having a mold body with a first sidewall, a second sidewall, and a bottom. The sidewalls and bottom define a recess for receiving an antibiotic-impregnated material. The recess includes depressed sections that are spaced apart by an inner section. The outer sections are transverse to a longitudinal axis of the mold. The inner section includes a keel that extends upward and has a height that sets a size of a femoral component produced using the mold. The keel is aligned with the notch when the piston is inserted within the mold. The notch and the keel may include one or more calibration markings that indicate increments of adjustments to the size of the femoral component and resulting flexion and extension gaps and joint space position.