Patent classifications
A61B17/8816
DISCHARGE DEVICE FOR BONE REPLACEMENT MATERIALS
A discharge device (1) comprising a housing (200), a container insert (300) rotatably arranged therein and a piston. A lateral cutout (205) is formed in one housing wall (204), and a lateral container opening (303) is formed in one container wall (304). In order to prevent the compound from being compressed as the compound is discharged, the lateral container opening extends continuously as far as the distal container end (302) without a region of the container wall adjoining the lateral container opening in the distal direction along the longitudinal axis. In order to make it easier to put in the compound, the wall thickness of the housing wall decreases continuously toward the lateral cutout (205). In order to prevent clogging of the piston, the cross section of the container insert widens continuously in the distal direction.
Bone treatment systems and methods
Systems and methods for treating vertebral compression fractures are discussed. In an embodiment, a method includes mixing bone cement precursors thereby causing a first chemical curing reaction characterized by a first time-viscosity profile, controllably applying energy to the bone cement from an external source to modify the first time-viscosity profile to a second time-viscosity profile, and injecting the cement into bone at a substantially constant viscosity greater than about 1000 Pa.Math.s to greater than about 5000 Pa.Math.s over an extended working time. In another embodiment, a bone cement injector system is provided that includes a first handle component that is detachably coupled to a second sleeve component having a distal end for positioning in bone and a flow channel extending through the first and second components. The system includes first and second thermal energy emitters for delivering energy to bone cement flows in a flow channel portion in the first and second components, respectively.
Non-compliant medical balloon having an integral woven fabric layer
A non-compliant medical balloon may be changed from a deflated state to an inflated state by increasing pressure within the balloon. The non-compliant medical balloon is composed of a woven fabric layer composed of at least two woven fabric fibers forming an angle. The angle remains substantially unchanged when the balloon changes from a deflated state to an inflated state.
HEIGHT RESTORING DEVICE, INSERTION APPARATUS HAVING A HEIGHT RESTORING DEVICE AND METHOD FOR RESTORING THE HEIGHT OF AND STABILISING THE SPINAL COLUMN
The invention relates to a height restoring device for restoring the height of and stabilizing the spinal column, in particular for stabilizing broken vertebral bodies or contused intervertebral discs, which device can be arranged in an insertion position in a compression-fractured vertebral body or between adjacent vertebral bodies and once there, can be transferred from the insertion position into an expansion position by means of an expansion apparatus.
DEVICE FOR APPLYING BONE REPLACEMENT PASTES
Device (1) for applying bone replacement pastes or bone cements, wherein the device (1) comprises: A) a container-like base part (4) with a first end (5), a second end (6) and a cavity (7), which defines a first longitudinal axis (3), is closed at the first end (5) and is open at the second end (6); and B) a filling piston (8) which can be inserted slidably into the cavity (7) and has a second longitudinal axis (10) and two or more hollow spaces (9) which extend through the filling piston (8) coaxially or parallel to the second longitudinal axis (10) and into which the cannula (13) of the applicator (2) can optionally be inserted.
Methods and Compositions For The Treatment of Degenerate Bone
The present disclosure relates to methods and compositions for the treatment of degenerate bone in a patient. In some embodiments, the methods and compositions disclosed herein are useful in the treatment, prevention, or in delaying the progression of a bone disease linked to bone degeneration, such as osteoarthritis (“OA”), rheumatoid arthritis, and avascular necrosis.
DELIVERY DEVICE FOR GRAFT MATERIAL
A method of delivering graft material to a surgical site includes positioning graft material in a tube of a delivery device. The tube defines an open end and a bend along its length. A plunger within the tube is advanced to dispense the graft material through the open end.
Systems and methods for promoting sacroiliac joint fusion
Embodiments are directed to fusion implants, insertion instruments, and methods of using the same for implanting one or more fusion implants across a sacroiliac joint and into an ilium and sacrum for fusing the sacroiliac joint. In some cases, fusion-promoting material may be inserted in the fusion implant for further promoting fusion across the sacroiliac joint. In some cases, neurophysiologic monitoring may be performed as the fusion implants are placed across the sacroiliac joint.
Bone graft delivery devices, systems and kits
A bone graft delivery kit includes a hollow tube having a proximal end and a distal end. The hollow tube is configured to convey graft material to a graft receiving area in a patient. The hollow tube can be connected to an implant. The kit further includes a plunger to facilitate moving the graft material through the hollow tube.
Spinal implant structure and kit thereof
The present invention provides a spinal implant structure. The spinal implant structure comprises a first part, a second part and at least one expansion arm. The second part is disposed on the horizontal orientation of the first part and does not overlap with the first part. The diameter of the first part is larger than that of the second part. One end of the expansion arm is connected to the first part, and the other end of the expansion arm is free end. The expansion arm includes a supporting arm. One end of the supporting arm is connected to the expansion arm, and the other end is connected the second part. The support arm includes a plurality of structure weakness. When the distance between the first part and the second part changes, the support arm bends from the structure weakness, thereby the spinal implant structure is expanded.