1465results about "Knee joints" patented technology

Knee replacement prosthesis are provided, comprising a plurality of sensors and at least one of a femoral component, a patellar prosthesis and a tibial component.

An orthopaedic system includes a tibial insert and a femoral component configured to articulate on the tibial insert. The tibial insert includes an articular surface, and the femoral component includes a femoral articular surface having decreasing radii of curvature posteriorly. The articular surface of the tibial insert includes an increased anterior lip to improve stability of the femoral component.

The invention provides a tibial plateau assembly and a knee joint prosthesis with the tibial plateau assembly.The tibial plateau assembly comprises a first driving part arranged on a tibial plateau and hinged to a tibial pad, the first driving part has a first driving state and a first static state, and when the first driving part is in the first driving state, the first driving part drives the tibial pad to rotate; the first driving piece can stretch out and draw back in the direction from the tibia platform to the tibia gasket; the second driving piece and the first driving piece are arranged on the tibia platform in a spaced mode, the second driving piece is hinged to the tibia gasket, the second driving piece has a second driving state and a second static state, and when the second driving piece is in the second driving state, the second driving piece can stretch out and draw back in the direction from the tibia platform to the tibia gasket; the first driving part and the second driving part are matched to adjust the distance and / or the inclination angle between the tibia gasket and the tibia platform. According to the technical scheme, the problem that the relative position between the tibia gasket and the tibia platform cannot be adjusted in the prior art is effectively solved.

The present application provides a pressure sensing device and system for a unicompartmental knee joint, belonging to the field of medical device technology. The device includes: a housing assembly, provided with a sealed receiving cavity; a flexible pressure sensing electrode layer, accommodated in the sealed receiving cavity, for detecting the pressure of the unicompartmental knee joint, and converting the pressure of the unicompartmental knee joint into a sensing capacitance signal, the flexible pressure sensing electrode layer includes a first electrode layer and a second electrode layer arranged in a stacked manner, the second electrode layer is coated with a dielectric layer on the side facing the first electrode layer, the dielectric layer is bonded to the second electrode layer on the side facing the second electrode layer, and a microstructure is formed on the dielectric layer on the side facing the first electrode layer; a signal processing module, accommodated in the sealed receiving cavity, electrically connected to the flexible pressure sensing electrode layer, for converting the sensing capacitance signal into a unicompartmental knee joint pressure value. The present application has good measurement accuracy and signal stability when used in unicompartmental knee replacement.

An orthopaedic knee prosthesis includes a tibial bearing component with articular features which operate to protect adjacent soft tissues of the natural knee, promote and / or accommodate desired articulation with an abutting femoral component, and facilitate expedient and effective implantation by a surgeon.

An orthopedic tibial prosthesis includes a tibial baseplate with an asymmetric periphery which promotes proper positioning and orientation on a resected tibia, while also facilitating enhanced kinematics, soft-tissue interaction, and long-term fixation of the complete knee prosthesis. The asymmetric baseplate periphery is sized and shaped to substantially match portions of the periphery of a typical resected proximal tibial surface, such that proper location and orientation is evident by resting the baseplate on the tibia. The baseplate periphery provides strategically positioned relief and / or clearance between the baseplate periphery and bone periphery, such as in the posterior-medial portion to prevent deep-flexion component impingement, and in the anterior-lateral portion to avoid undue interaction between the anatomic iliotibial band and prosthesis components.

An implant includes a body including a substrate and a bone interfacing lattice disposed on the substrate. The bone interfacing lattice includes at least two layers of elongate curved structural members. In addition, the at least two layers of elongate curved structural members include a first layer adjacent the substrate and a second layer adjacent the first layer. Also, the first layer has a first compressibility and the second layer has a second compressibility, wherein the second compressibility is greater than the first compressibility. Further, an interface between the first layer and the second layer is a transition region having a thickness within which the elongate curved structural members of the first layer are intermingled with the elongate curved structural members of the second layer such that a boundary of the first layer overlaps with a boundary of the second layer.

The invention provides a knee joint prosthesis tibial plateau capable of enhancing fixation and a tool matched with the tibial plateau, the knee joint prosthesis tibial plateau specifically comprises a tibia support, the tibia support is of a hollow cylinder structure, and three convex bodies are fixedly arranged on the outer surface of the tibia support; a groove penetrating into the tibia support is formed in the abutment, and the abutment is fixedly arranged on the tibia support; the pushing device comprises extension rods arranged at the two ends of a worm, the worm with threads arranged on the outer surfaces of the two ends, turbines arranged on the two sides of the worm, upper supporting bodies arranged at the tops of the turbines and connected with the fixing device through first connecting bodies, and lower supporting bodies arranged at the bottoms of the turbines and connected with the fixing device. The fixing device is a hollow cone, a first spring is arranged in the fixing device, one end of the first spring is connected with the first connector, and the other end of the first spring is connected with a fixing block. According to the technical scheme, the technical problem that after the knee joint prosthesis is implanted into the tibia, the tibial plateau is unstable, the prosthesis is loosened and disengaged, and then bone fusion is affected is effectively solved.

A rotary tool includes a tool body and a powered rotary cutting tooltip that is oriented and positioned relative to the tool body by a plurality of processor-controlled actuators that provide degrees of freedom. The processor uses a surgical tracking system to identify the pose of the tool body and the tooltip relative to a patient's anatomy and controls the actuators to maintain the tooltip within a predetermined cutting plan to compensate for deviation of a surgeon's hand or a robotic arm controlling the tool body during a cutting operation.

An assembly for making an intramedullary spacer made of medical cement, designed to be inserted in a medullary canal. The assembly includes comprising a stem module and a reinforcing core. The stem module includes an end wall delimiting below a stem moulding chamber (SMC); and wherein the reinforcing core is at least partly positioned in the stem moulding chamber (SMC).

An orthopaedic knee implant includes a femoral component having a substrate and a coating disposed on the surface of the substrate. A method for making a femoral component of an orthopaedic knee implant is also disclosed.

The invention relates to a tibial plateau prosthesis. The tibial plateau prosthesis mainly comprises a tibial spacer, a tibial plateau and a sleeve. The tibia gasket is provided with a first fixing block and three arc-shaped holes, and movable second fixing blocks are arranged in the holes. The tibial plateau comprises a plateau support with open holes and a shell, and the open holes are formed in the side portion and the bottom of the shell. The screw penetrates through the gasket and the platform support to be inserted into the shell, and outer threads of the screw are meshed with inner threads of the sleeve. The sleeve moves upwards and extends out of the side hole of the shell through a hinged connecting rod system to penetrate into the medullary cavity to enhance fixation. A spring is arranged in the screw to drive the first pushing part and can be matched with the sleeve to prevent downward movement; and meanwhile, the second pushing part in the screw can extend into the medullary cavity from the bottom through threads. The design realizes multidirectional fixation and improves the stability of the prosthesis.

A proximal femur replacement implant assembly (500, 1000) arranged and configured to replace a head portion of a patient's proximal femur is disclosed. In some examples, the proximal femur replacement implant assembly includes a proximal femur replacement implant (505, 1005) arranged and configured to be coupled to, or inserted into an intramedullary canal of, a remaining portion of a patient's femur. The proximal femur replacement implant being arranged and configured to engage a bone plate (510, 1010, 1050) to, for example, minimize micromotion of the patient's greater trochanter to promote porous in-growth and to constrain movement of the greater trochanter.

The invention discloses a multi-node wearable and implantable joint intelligent monitoring linkage device and method, and relates to the field of joint monitoring, and the device comprises an in-vitro multi-node wearable module and an in-vivo implantable intelligent joint prosthesis; the in-vitro multi-node wearable module and the in-vivo implantable intelligent joint prosthesis cooperatively analyze the rehabilitation state of a patient implanted with the artificial joint; the in-vitro multi-node wearable module comprises a first main control chip, a first IMU (Inertial Measurement Unit) chip and a Bluetooth chip; the in-vivo implanted intelligent joint prosthesis comprises a joint prosthesis body, a second main control chip, a second IMU chip and an NFC tag chip, wherein the second main control chip, the second IMU chip and the NFC tag chip are arranged in the joint prosthesis body. In-vitro data are collected in real time through the first IMU chip in the in-vitro multi-node wearable module, joint movement data are collected in real time through the second IMU chip in the in-vivo implanted intelligent joint prosthesis, and real-time monitoring of knee hip joints and other parts of the body is achieved.

Prosthetic devices allow for full articulation of the joint, while absorbing impact of the components during normal use that will reduce wear on the device components and prolong life. The device may include a bone implantable component and a bearing component having an articulation surface that is sized and shaped to substantially mate with at least a portion of the bone implantable component and a damping mechanism that includes a contact member disposed at least primarily inside a cavity; a biasing member biasing the contact member toward an upper aperture of the cavity and means for capturing the contact member within the cavity.

Orthopedic implants and related surgical methods for using same. The implants have suture bore geometries that facilitate performance of the surgical methods, thereby providing for improved optimal biomechanical force application in various anatomies. The implants include suture bores that have an angled / diagonal, or skewed, orientation within the anatomical planes (lateral / sagittal and frontal / coronal). The suture bores have the skewed orientation so that the adjacent soft tissues (i.e., tendons or ligaments) can be advanced via the suture therethrough in superior-inferior and inferior-superior directions. Openings, or holes, at the ends of the suture bores are configured to approximate the adjacent associated soft tissue to the implant.

A system for surgical registration. The system may include at least one computing device in communication with a surgical navigation system and the surgical device. The at least one computing device: a) receiving external bone registration data corresponding to locations on the exterior surface of the femur; b) calculating a first registration transform based on the external bone registration data; c) transforming a first bone removal plan of a surgical plan to the operative coordinate system based on the first registration transform; d) receiving internal bone canal registration data corresponding to at least one of location or orientation data from the inner canal of the femur; e) calculating a second registration transform based on both of the external and internal bone canal bone registration data; and f) transforming a second bone removal plan of the surgical plan to the operative coordinate system based on the second registration transform.

The embodiment of the invention is suitable for the technical field of computer-aided medical treatment and surgical planning, and provides a single-condyle surgical prosthesis planning method and device and computer device.The method comprises the steps that parameter information of a prosthesis to be planned is obtained, and the parameter information comprises the osteotomy amount; according to the parameter information, determining a placement position of the prosthesis in a pre-constructed three-dimensional model; calculating a coverage rate between a prosthesis section and a corresponding bone section in the three-dimensional model when the prosthesis is located at the placement position; according to the coverage rate, a target prosthesis is determined from the multiple to-be-planned prostheses, and preoperative planning of the unicompartmental condyle operation is carried out based on the target prosthesis. By the adoption of the method, the posture of the prosthesis can be automatically planned according to the osteotomy amount of the prosthesis, then the optimal prosthesis is selected for preoperative planning through calculation of the coverage rate of the section of the prosthesis, and the precision and safety of single-condyle surgery prosthesis planning are guaranteed.

According to one example, a tibial prosthesis that can include a tibial bearing component, tibial baseplate, an insert and a fastener. The tibial bearing component can have medial and lateral proximal articular surfaces and an opposing distal surface. The tibial bearing component can define at least one recess therein with the recess having an opening at a periphery of the tibial bearing component. The tibial baseplate can be coupled to the tibial bearing component on the proximal surface thereof and having a distal surface configured to be disposed on a resected proximal surface of a tibia. The insert can be configured to be disposed within the recess and can engage the tibial baseplate and the tibial bearing component. The fastener can be insertable into the tibial bearing component and can be configured to retain the insert to the tibial baseplate.

According to one example, a posterior-stabilized femoral prosthesis for a knee arthroplasty. The femoral prosthesis can include medial and lateral condyles, a femoral cam and a recess. The medial and lateral condyles can be shaped to articulate with a tibial articular surface of a tibial bearing component through a range of motion, in which full extension corresponds to zero degrees flexion of a knee joint and positive flexion corresponds to greater than zero degrees flexion of the knee joint. In a sagittal plane, the medial and lateral condyles can define medial and lateral multi-radius curves, respectively. The medial multi-radius curve can have a single common radius swept through a first angular extent to define a single arc length that extends from between substantially -20 degrees flexion to substantially 90 degrees flexion, inclusive.

The invention relates to a bionic meniscus 3D printing method and system, and the method comprises the steps: reading a meniscus STL model, carrying out the data preprocessing of the data of the model, and carrying out the construction to obtain a concave envelope contour; performing offset processing and four-curve segmentation to generate an elliptic equation fiber field; establishing a bidirectional mapping relation between a parameter space of an elliptic equation fiber field and a meniscus physical space based on an RBF mapping theory; based on a meniscus fiber density gradient change theory, performing simulation in a parameter space of the elliptic equation fiber field to obtain a bionic gradient fiber field; according to the meniscus STL model, the bidirectional mapping relation and the bionic gradient fiber field, fiber path coordinates of a meniscus physical space are obtained, and a 3D printing path is generated; and printing according to the 3D printing path to obtain the bionic meniscus. Precise simulation of a natural meniscus complex fiber structure is achieved through mathematical modeling, and the technical problems that in the prior art, fiber field control precision is insufficient, and regional characteristics are difficult to achieve are solved.

The invention provides a medical implant, a preparation method thereof and an artificial knee joint. The medical implant comprises a macromolecular porous stent and a hydrogel composite material at least filled in pores of the macromolecular porous stent, and the material of the macromolecular porous stent comprises a degradable macromolecular material and carbon nanotubes distributed in the degradable macromolecular material. The hydrogel composite material comprises a hydrogel material matrix and seed cells distributed in the hydrogel material matrix. According to the invention, the degradable high polymer material and the hydrogel material are combined, the carbon nanotubes are introduced into the degradable high polymer material, and meanwhile, seed cells are arranged in a hydrogel material matrix, so that the implantable stent material which has proper degradation performance and good mechanical properties and is renewable is provided.

The invention provides a data processing method, medium and equipment in knee arthroplasty, and belongs to the technical field of medical electronics. The method comprises the following steps: acquiring pressure distribution data, measured by an array sensor, of an articular compartment in a complete period of joint movement; based on the pressure distribution data, pressure centers under all buckling degrees in the whole period of joint movement are calculated, and corresponding pressure center tracks are formed; calculating shear stress distribution data under the complete period of joint movement based on the pressure center track data; based on the pressure distribution data, calculating a dynamic pressure envelope line under the complete period of the joint movement; and generating an intraoperative correction suggestion for knee arthroplasty based on the pressure center trajectory, the shear stress distribution data and the dynamic pressure envelope. The correction suggestions given by the method are more accurate for abnormal conditions occurring in knee replacement.

The invention comprises a system for securing an implant to a bone comprising an implant which is affixed to the bone, a grout or bone cement comprising a composition that cures in an exothermic reaction and which is capable of securing the implant to the bone in a cured state, a device which provides access to the grout or bone cement in position on the bone and a tester which measures temperature over time to detect the exothermic reaction so as to determine when the composition reaches cure. The tester comprises a sensor joined to a circuit and to an indicator that emits a signal in response to a current emitted to the circuit by the sensor.

An insert for use in a knee prosthesis is disclosed. In one embodiment, the insert includes a medial compartment and a lateral compartment. The medial compartment includes a top surface having a concave surface or curve with a more posterior sulcus and increased anterior lip. The lateral compartment includes a top surface having at least a segment or portion with a convex surface or curve. Thus arranged, the insert is arranged and configured to provide improved stability for varying grades of PCL deficiencies compared to existing inserts that have a mid-line sulcus and lateral convexity. In addition, the insert provides improved lateral posterior translation compared to existing designs with a concave or flat lateral articulation that lack a lateral posterior convexity.

To provide, e.g., a stem provisional assembly that can be configured to be moveable in vivo to position a stem provisional assembly within a bone recess.SOLUTION: According to one example, a provisional system for a knee arthroplasty is disclosed. The system can include any one or combination of a first provisional component 212, a second provisional component 154, a stem provisional assembly 124 and a fastener 214. The first provisional component can be configured to be disposed on a resected bone surface. The second provisional component can be configured to be disposed in a first recess beneath the resected bone surface. The stem provisional assembly can be configured to be disposed in a second recess, and is configured to be engageable in vivo to position the first provisional component on the resected bone surface. The fastener can be configured to couple the first provisional component, the second provisional component and the stem provisional assembly together as an assembly.SELECTED DRAWING: Figure 19

To provide, e.g., a stem provisional assembly that can be configured to be moveable in vivo to position a stem provisional assembly within a bone recess.SOLUTION: According to one example, a provisional system for a knee arthroplasty is disclosed. The system can include any one or combination of a first provisional component 212, a second provisional component 154, a stem provisional assembly 124 and a fastener 214. The first provisional component can be configured to be disposed on a resected bone surface. The second provisional component can be configured to be disposed in a first recess beneath the resected bone surface. The stem provisional assembly can be configured to be disposed in a second recess, and is configured to be engageable in vivo to position the first provisional component on the resected bone surface. The fastener can be configured to couple the first provisional component, the second provisional component and the stem provisional assembly together as an assembly.SELECTED DRAWING: Figure 19

There is provided a tibial component comprising a tibial tray having a superior side and an inferior side, and a support member connected to the inferior side of the tibial tray, the support member having a stem portion, the stem portion including one or more fins and a first arm angled relative to a second arm. In one form, the fins have a curvature that extends away from the stem portion. In another form, the first arm defines an opening sized to receive an anchor wherein the anchor is configured to penetrate a portion of bone and the opening in the first arm. Optionally, the stem portion includes a first portion having a first cross sectional area and a second portion having a second cross sectional area wherein the first cross sectional area is larger than the second cross sectional area. The fins and arms can include rail protrusions.

The present disclosure provides alert implants that comprise a medical device and an implantable reporting processor (IRP), where one example of such a medical device includes a component for a total knee arthroplasty (TKA) such as a tibial extension, a femoral component for hip replacements, a breast implant, a distal rod for arm or leg breakage repair, a scoliosis rod, a dynamic hip screw, a spinal interbody spacer, and tooling and methods that may be used to form the alert implant, and uses of such alert implants in the health maintenance of patients who receive the implant.

According to one example, a for revision knee arthroplasty is disclosed. According to this example, the method can include shaping a bone of a patient to create one or more recesses therein, selecting a stem provisional, disposing the stem provisional within the one or more recesses, and assembling in vivo the stem provisional with both a first provisional component configured to simulate a shape of one of a tibial tray implant or a femoral implant and a second provisional component configured to simulate a shape of at least one of a sleeve component, a cone component or a keel component of an implant.