Class / Patent application number | Description | Number of patent applications / Date published |
623200130 | Leaflet made of biological tissue | 78 |
20090018649 | REINFORCEMENT DEVICE FOR A BIOLOGICAL VALVE AND REINFORCED BIOLOGICAL VALVE - A reinforcement device for a biological valve includes an arrangement of supports configured to establish a double-trigone geometry in the valve and coupled to a base upon which the valve may be mounted. A plurality of commissural supports establish the geometry of a commissural trigone, and a plurality of intercommissural supports establish the geometry of an intercommissural trigone. A method for reinforcing a biological valve includes using commissural supports in conjunction with intercommissural supports, both sets of supports coupled to a base upon which the valve is mounted. | 01-15-2009 |
20090030511 | Percutaneously implantable replacement heart valve device and method of making same - A method of making a replacement heart valve device whereby a fragment of biocompatible tissue material is treated and soaked in one or more alcohol solutions and a solution of gluteraldehyde. The dried biocompatible tissue material is folded and rehydrated in such a way that forms a two- or three-leaflet/cusp valve without affixing of separate cusps or leaflets or cutting slits into the biocompatible tissue material to form the cusps or leaflets. After the biocompatible tissue material is folded, it is affixed at one or more points on the outer surface to the inner cavity or a stent. | 01-29-2009 |
20100131053 | METHODS OF REDUCING RETROGRADE FLOW - Methods of reducing retrograde fluid flow through a valve within a body vessel are provided. The methods can include the steps of identifying a valve exhibiting an undesirable amount of retrograde fluid flow within a body vessel, such as a venous valve or a heart valve, and providing a means for reducing the retrograde fluid flow. A medical device providing a desired amount of retrograde fluid flow can be modified after permitting the medical device to remain in a body cavity for a remodeling-effective time period. The implanted medical device can be modified by subsequently reducing the amount of retrograde fluid flow permitted across the implanted prosthetic valve within the body vessel. | 05-27-2010 |
20100222877 | Tissue Engineered Human Pulmonary Valves with Cyclic Pressure Bioreactor Accelerated Seeding Strategies and Methods For Assessing Inflammatory Potential of Putative Scaffolds for Tissue Engineered Heart Valves - The invention provides for bioengineered or tissue engineered heart valves that are more efficiently recellularized and/or have a decreased inflammatory potential. The heart valves are generally decellularized and then recellularized using autologous cells wherein the valves are subjected to pulsatile motion during the recellularization process. Tissue engineered heart valves subjected to the pulsatile motion are characterized by having at least 20% of the cells that remain on or in said previously decellularized tissue two weeks after the recellularization process are located below or interior to the basement membrane of said tissue. A method of making bioengineered tissues having these characteristic is also disclosed. Further provided is a bio-assay and related method for determining the inflammatory potential of a tissue. | 09-02-2010 |
20110060406 | HEART VALVE - The new valve has a ring ( | 03-10-2011 |
20110238167 | METHODS OF CONDITIONING SHEET BIOPROSTHETIC TISSUE - Methods for the conditioning of bioprosthetic material employ bovine pericardial membrane. A laser directed at the fibrous surface of the membrane and moved relative thereto reduces the thickness of the membrane to a specific uniform thickness and smoothes the surface. The wavelength, power and pulse rate of the laser are selected which will smooth the fibrous surface as well as ablate the surface to the appropriate thickness. Alternatively, a dermatome is used to remove a layer of material from the fibrous surface of the membrane. Thinning may also employ compression. Stepwise compression with cross-linking to stabilize the membrane is used to avoid damaging the membrane through inelastic compression. Rather, the membrane is bound in the elastic compressed state through addition cross-linking. The foregoing several thinning techniques may be employed together to achieve strong thin membranes. The finally thinned membrane may then be treated by capping of calcification nucleation sites and borohydride reduction. The leaflets may be formed to have more than one region of uniform thickness, such as a thicker peripheral sewing region. | 09-29-2011 |
20120185038 | PERCUTANEOUSLY DELIVERABLE HEART VALVE INCLUDING FOLDED MEMBRANE CUSPS WITH INTEGRAL LEAFLETS - A transcatheter, percutaneously implantable, prosthetic heart valve is provided that comprises a lattice frame and two or more integrated cusp and leaflet folded structures attached to the lattice frame. The two or more integrated cusp and leaflet folded structures each comprise a flat sheet of biocompatible membrane that is folded to include a substantially conical shape according to a flat folding pattern. The substantially conical shape is further formed by joining apposing sides of the substantially conical shape along a seam. The two or more integrated cusp and leaflet folded structures are each attached along their respective seams to the lattice frame in a direction substantially parallel to an axis of the lattice frame. Embodiments of valves described herein have application within the entire vascular system. | 07-19-2012 |
20120316642 | INVASIVE CARDIAC VALVE - An invasive cardiac valve comprises a tubular stent ( | 12-13-2012 |
20130030521 | DEVICES FOR REDUCING LEFT ATRIAL PRESSURE HAVING BIODEGRADABLE CONSTRICTION, AND METHODS OF MAKING AND USING SAME - A device for regulating blood pressure between a patient's left atrium and right atrium comprises an hourglass-shaped stent comprising a neck region and first and second flared end regions, the neck region disposed between the first and second end regions and configured to engage the fossa ovalis of the patient's atrial septum; and a one-way tissue valve coupled to the first flared end region and configured to shunt blood from the left atrium to the right atrium when blood pressure in the left atrium exceeds blood pressure in the right atrium. The inventive device may include a biodegradable material that biodegrades to offset flow changes caused by tissue ingrowth. The inventive device may reduce left atrial pressure and left ventricular end diastolic pressure, and may increase cardiac output, increase ejection fraction, relieve pulmonary congestion, and lower pulmonary artery pressure, among other benefits. | 01-31-2013 |
20130066418 | PROSTHETIC TISSUE VALVE - A prosthetic tissue valve for aortic, pulmonary, mitral or tricuspid valve replacement is described herein. A sewing ring for use with the prosthetic tissue valve is also described. The valve can have a circumference that is a predetermined distance larger than the circumference of an annulus in a defective valve. The valve can be substantially planar in an unstressed position before attachment at the annulus and substantially non-planar upon attachment in a biased position at the annulus. The valve can have a multi-lobal shape in the unstressed position. Methods are provided for placing the valve as described herein in the biased position within the annulus of the defective valve. | 03-14-2013 |
20130116778 | Replacement Heart Valve Leaflet Stitching Method and Device - A replacement heart valve and stitching method for reducing the unexpanded profile of the replacement heart valve are herein provided. The method includes whip stitching a plurality of leaflets together with a first whip stitch pattern a second whip stitch pattern which overlaps the first whip stitch pattern and is wound in an opposite direction. The method further involves securing the valve leaflets to one another via a running stitch. | 05-09-2013 |
20130190860 | PERCUTANEOUSLY DELIVERABLE VALVES - This document provides methods and materials related to providing a mammal with a replacement valve (e.g., a synthetic or artificial heart valve). For example, synthetic or artificial heart valve that can be delivered in a minimally invasive manner are provided. | 07-25-2013 |
20130211511 | METHOD OF USING AMNION ALLOGRAFT IN HEART VALVE REPLACEMENT SURGERY - Improved methods for heart valve replacement surgery are described. The methods utilize an allograft comprising a layer of amnion to improve the performance and reduce complications of heart valve replacement surgery and the allograft has a pre-made size and shape suitable for the application. | 08-15-2013 |
20130226291 | IMPLANTABLE VASCULAR DEVICE - A valve prosthesis, such as an artificial venous valve, is described. The valve prosthesis has a support frame formed from a cannula and an attached covering that defines an opening adapted to move between a first position in which the opening is open to fluid flow and a second position in which the opening is closed to fluid flow. The support frame includes a leaflet support portion and a circumferential centering support element disposed adjacent the leaflet support portion with respect to a lengthwise axis of the support frame and mirroring the leaflet support portion with respect to a transverse axis of the support frame. | 08-29-2013 |
20130310929 | METHODS OF CONDITIONING SHEET BIOPROSTHETIC TISSUE - Methods for the conditioning of bioprosthetic material employ bovine pericardial membrane. A laser directed at the fibrous surface of the membrane and moved relative thereto reduces the thickness of the membrane to a specific uniform thickness and smoothes the surface. The wavelength, power and pulse rate of the laser are selected which will smooth the fibrous surface as well as ablate the surface to the appropriate thickness. Alternatively, a dermatome is used to remove a layer of material from the fibrous surface of the membrane. Thinning may also employ compression. Stepwise compression with cross-linking to stabilize the membrane is used to avoid damaging the membrane through inelastic compression. Rather, the membrane is bound in the elastic compressed state through addition cross-linking. The foregoing several thinning techniques may be employed together to achieve strong thin membranes. | 11-21-2013 |
20140180399 | MESH ENCLOSED TISSUE CONSTRUCTS - Described is a heart valve leaflet manufactured from a mesh material. The mesh material may have an ability to capture circulatory/stationary/migratory cells of the body to become biologically active. In some cases, the mesh material is coated with a bioactive material, such as a molecule that binds to a cell adhesion molecule (CAM), a growth factor, an extracellular matrix molecule, a subendothelial extracellular matrix molecule or a peptide. The mesh has a stiffness that is comparable to a native heart valve leaflet, such that it functionally mimics a native heart valve. | 06-26-2014 |
20140188218 | Extracellular Matrix Material Conduits and Methods of Making and Using Same - Extracellular matrix (ECM) valve conduits are disclosed. Methods for regenerating atrioventricular valves to replace defective atrioventricular valves within a heart of a subject using the ECM valve conduits are also disclosed. Methods of sterilizing and decellularizing an ECM material are also disclosed. | 07-03-2014 |
20140200659 | CAPPING BIOPROSTHETIC TISSUE TO REDUCE CALCIFICATION - A treatment for bioprosthetic tissue used in implants or for assembled bioprosthetic heart valves to reduce in vivo calcification. The method includes applying a calcification mitigant such as a capping agent or an antioxidant to the tissue to specifically inhibit oxidation in tissue. Also, the method can be used to inhibit oxidation in dehydrated tissue. The capping agent suppresses the formation of binding sites in the tissue that are exposed or generated by the oxidation and otherwise would, upon implant, attract calcium, phosphate, immunogenic factors, or other precursors to calcification. In one method, tissue leaflets in assembled bioprosthetic heart valves are pretreated with an aldehyde capping agent prior to dehydration and sterilization. | 07-17-2014 |
20140243964 | SUTURELESS PROSTHETIC DEVICE - A prosthetic device for use in an anatomical orifice or lumen of a patient includes an expandable first stent structure coupled to a valve support structure having at least one leaflet. The stent structure includes a collar provided with at least one groove or opening adapted to engage a tab extending from the valve support structure. Rotation of the stent structure and valve support structure relative to one another assembles the prosthetic valve device. The prosthetic valve device may be used for sutureless treatment of various valvular conditions such as aorta stenosis and mitral valve replacement. | 08-28-2014 |
20140257472 | METHOD OF PREPARING A TISSUE SWATCH FOR A BIOPROSTHETIC DEVICE - A method of preparing a tissue swatch comprising one or more desired thicknesses for use in the manufacture of a bioprosthetic device, said method comprising sectioning a sheet of frozen tissue to produce a tissue swatch of said one or more desired thicknesses. | 09-11-2014 |
20140288641 | OXIDATION RESISTANT BIOPROSTHETIC TISSUES AND PREPARATION THEREOF - Oxidation resistant bioprosthetic tissues and oxidation resistant bioprosthetic heart valve leaflets are described. Also provided are methods for preparing the oxidation resistant bioprosthetic tissues and bioprosthetic heart valve leaflets, and methods for preventing oxidative degeneration in bioprosthetic tissues, including immobilizing covalently an effective amount of an antioxidant to the bioprosthetic tissue. | 09-25-2014 |
20140358223 | PROSTHESES - The disclosure provides valve prostheses and methods of installation. One embodiment of the prosthesis has a generally tubular body adapted for placement proximate a mitral annulus. The tubular body has a generally tubular upper portion adapted to substantially reside in the left atrium above the mitral annulus. The generally tubular upper portion has a first circumferential wall that is outwardly biased to urge against cardiac tissue of the left atrium. The tubular body also includes a lower portion extending downwardly from the generally tubular upper portion, the lower portion being configured to substantially reside in the left ventricle below the mitral annulus. The lower portion of this embodiment can be defined by an generally circumferential wall that extends downwardly from the generally tubular upper portion. The generally circumferential wall has a first circumferential end and a second circumferential end, and defines a circumferential extent therebetween. | 12-04-2014 |
20150100118 | METHOD FOR DIRECTING CELLULAR MIGRATION PATTERNS ON A BIOLOGICAL TISSUE - A contoured biological tissue for a bioprostheses, such as a cardiac/vascular patch or a bioprosthetic heart valve, and methods of contouring the tissue, are described. A predetermined pattern is provided on the tissue, comprising a plurality of ridges or depressions that are configured to facilitate cellular migration in a first direction and discourage cellular migration in a second direction. The biological tissue can be used in connection with a bioprosthetic heart valve comprising a biological tissue leaflet structure coupled to a supporting frame. | 04-09-2015 |
20150148897 | ARTIFICIAL TISSUE - A method of forming a matrix of aligned nanofibres of elevated pore size and porosity comprises spraying a polymer solution towards a rotating drum so as to form nanofibres which are collected on the drum. The matrix can be used to form artificial tissue by removing the matrix from the drum, depositing cells onto the matrix and allowing the cells to form artificial tissue. Such artificial tissue finds use in the treatment of disease or damaged tissue, and in particular in the treatment of cardiovascular disease. | 05-28-2015 |
20150306281 | DEVICES AND METHODS FOR INHIBITING STENOSIS, OBSTRUCTION, OR CALCIFICATION OF A NATIVE HEART VALVE, STENTED HEART VALVE OR BIOPROSTHESIS - The present invention relates to methods for inhibiting stenosis, obstruction, or calcification of a valve following implantation of a valve prosthesis or a native valve which develops disease via the Lrp5/Wnt Pathway in the presence of elevated lipids due to elevated Low Density Lipoprotein. This invention involves dispensing a combination of medications to target inflammation and attachment of the target cell and the secondary drugs to inhibit proliferation and calcification on an elastical stent, gortex graft or valve leaflet. The combination therapy inhibits bioprosthesis and native valve calcification with improvement of the longevity of the prosthetic material including the stent, the native valve, and the gortex covering. The valve prosthesis and or gortex graft is mounted on the elastical stent or prosthesis such that the elastical stent is connected to the valve. | 10-29-2015 |
20160175096 | PROSTHETIC VALVES WITH MECHANICALLY COUPLED LEAFLETS | 06-23-2016 |
20140012388 | RADIAL HEAD PROSTHESES AND TRIALS - Radial head prostheses and trialing devices. A radial head prosthesis includes a head component and a stem component, and may include an intermediate component. The head component may be offset from the stem component. The head component includes a bearing surface having an axis of rotation, which may be radially and/or angularly offset from the central longitudinal axis of the stem component. A radial head trialing device may include cutting edges for resection of a distal radius. Another trialing device may allow for adjusting the radial offset and/or angular position of a trial head component from a trial stem component. | 01-09-2014 |
623200140 | Supported by resilient frame | 39 |
20080275558 | EXTRA-ARTICULAR IMPLANTABLE MECHANICAL ENERGY ABSORBING SYSTEMS AND IMPLANTATION METHOD - A system and method for sharing and absorbing energy between body parts. In one aspect, the method involves identifying link pivot locations, fixing base components and minimally invasive insertion techniques. In one particular aspect, the system facilitates absorbing energy between members forming a joint such as between articulating bones. | 11-06-2008 |
20080275559 | ADJUSTABLE ABSORBER DESIGNS FOR IMPLANTABLE DEVICE - A system for manipulating energy transferred by members defining a joint. The system includes a first attachment structure configured to be attached to a first member of the joint and a second attachment structure configured to be attached to a second member of the joint. There is also an adjustable energy absorbing device attached to the first attachment structure and second attachment structure, wherein adjusting the energy absorbing device changes the load manipulating characteristics of the energy absorbing device. | 11-06-2008 |
20080306602 | Tibia Cement Impaction System - A tibial cement impaction system and method are characterized by disposable frame and plunger elements which are used to drive bone cement under pressure into apertures formed in the top surface of the tibia to prevent a subsequently applied tibia plate or component of a knee prosthesis from loosening from the tibia. To prepare the tibia, the surgeon removes the top damaged surface of the tibia to define a relatively flat surface and drills a plurality of small holes or apertures into the surface. The holes are spaced across the surface. Next, the surgeon arranges the frame over the prepared tibia surface. The frame includes a wall having a generally kidney-shaped configuration which matches the outer perimeter of the top portion of the tibia and defines a chamber. Bone cement is arranged in the chamber and then the plunger, which is configured to match the contour of the wall, is pressed into the chamber, forcing the bone cement into the apertures and evenly across the top surface of the tibia. The plunger and frame are removed and discarded. Next, the tibia plate is arranged on the bone cement and driven against the tibia with the stem portion of the plate extending through the cement into the tibia. When the cement hardens, the plate is securely connected with the tibia. | 12-11-2008 |
20090036992 | Total Knee Arthroplasty Endoprothesis with Third Condyle and Rotating Polyethylene Insert - The invention presents a total knee arthroplasty endoprosthesis having: a) a femoral component with a lower-radius lateral condyle, a larger-radius medial condyle and between them, a third condyle located posteriorly, superiorly and nearest the medial side, b) a tibial component with a central protruding spigot for the rotating polyethylene insert, and c) a rotating polyethylene insert, with three cavities for articulation of the femoral condyles. For initial and moderate flexion the joint functions with load bearing onto the lateral and medial articular cavities, and in advanced and final flexion with load bearing on the third articular cavity. The advantages of this endoprosthesis are enhanced maximum flexion, improved femoral axis alignment, significant posterior stabilization, favourable accommodation of tibial rotation with consequent relief of materials and fixations, and preservation of more articular fluid for lubrication and reduction of polyethylene wear. | 02-05-2009 |
20090048680 | ARTIFICIAL JOINT AND A JOINT PART INTENDED FOR THIS PURPOSE - An artificial joint as an endoprosthesis for a human joint, including a first joint part having two first functional surfaces, a second joint part having two second functional surfaces, the two first and second functional surfaces of each joint part being convex-concave, concave-convex, or convex-convex in a proximal-distal direction, a projection associated with the first joint part; and a recess associated with the second joint part. The recess is configured to engage with the projection so as to determine a relative position of the first and second joint parts in a transverse plane of the joint and to form a stop for a sliding movement of the first and second joint parts relative to each other. The two first functional surfaces are pivotable about a pivot axis with respect to the second functional surfaces and each of the first functional surfaces rolls and slides with respect to the second functional surfaces during an extension or flexion of the artificial joint. A respective posterior position in each angular position is determined as a function of the extension/flexion of the first and second joint parts so as to at least partially delimit a posterior sliding movement of first joint relative to the second joint part. | 02-19-2009 |
20090088859 | FIXED-BEARING KNEE PROSTHESIS HAVING INTERCHANGEABLE COMPONENTS - A fixed-bearing prosthesis includes a femoral component having a medial condyle surface and a lateral condyle surface. The knee prosthesis also includes a bearing having a medial bearing surface configured to articulate with the medial condyle surface of the femoral component, and a lateral bearing surface configured to articulate with the lateral condyle surface of the femoral component. A tibial tray is secured to the bearing. The tibial tray has a platform with an elongated stem extending downwardly from a lower surface thereof. A posterior buttress extends along a posterior section of the perimeter of the tray's platform, and an anterior buttress extends along an anterior section of the perimeter of the tray's platform. Differently-sized tibial trays are interchangeable with differently-sized bearings. | 04-02-2009 |
20090125114 | KNEE JOINT PROSTHESIS SYSTEM AND METHOD FOR IMPLANTATION - A system for cooperating with an elongated IM member during preparation of a bone for receiving a prosthesis can include a scaffold, skeleton or frame. An alignment assembly can be selectively coupled to the frame. The alignment assembly can cooperate with the IM member to position the frame relative to the bone. A cutting block can be selectively coupled to the frame. According to other features, a posterior stabilized (PS) box guide assembly can have a PS box guide attachment portion that selectively couples with the first attachment portion of the frame. A posterior foot can selectively couple with a second attachment portion on the frame. The posterior foot can be positioned to occupy space of a joint line in an installed position. | 05-14-2009 |
20090125115 | KNEE SYSTEM AND METHOD OF MAKING SAME - A femoral prosthesis may be formed as a femoral component incorporating a base material and an articulating material. In one exemplary embodiment, the base material is a metal and the articulating material is a polymer. Specifically, the base material provides strength and rigidity to the femoral component, while the articulating material contacts a tibial prosthesis or natural tibia during joint articulation. In one exemplary embodiment, the articulating material forms the articulating surface of one or more condyle portions of the femoral component. | 05-14-2009 |
20090171463 | Arthrodesis module and method for providing a patient with an arthrodesis - An endoprothetical connection element for creating a knee arthrodesis comprises a coupling element that comprises a first fastener and a second fastener. The first fastener is adapted for connection with a first fastening element corresponding to the first fastener that is provided at a shaft insertable into a femur of a patient. The second fastener is adapted for connection with a second fastening element corresponding to the second fastener that is provided at a shaft insertable into a tibia of the patient. The coupling element is formed such that a first longitudinal axis of the femoral shaft connected to the first fastener and a second longitudinal axis of the tibial shaft connected to the second fastener include an angle different from 180 degrees which, when implanted into the body of the patient, is lying in a coronal plane of the patient. | 07-02-2009 |
20090187250 | JOINT - An artificial joint as an endoprosthesis for a human joint, has at least two joint parts wherein each joint part has two functional surfaces that operatively interact with each other, one associated with the first joint part and the other with the second joint part. The two functional surfaces of each joint part are spheroidal in shape and convex-concave, concave-convex or convex-convex in shape in the proximal-distal arrangement, and the functional surfaces can each pivot around a pivoting axis. In order to create an artificial joint as an endoprosthesis for a human joint, whose motion behavior is perceptibly improved for the patient, the two pivoting axes of the two functional surfaces of each joint part are slanted towards each other. | 07-23-2009 |
20100070045 | System and Method for Joint Resurface Repair - An implant for installation into a portion of an articular surface includes a protrusion configured to cover an un-excised portion of articular surface proximate to the implant. Another implant may form a cavity to allow the un-excised portion of articular surface to remodel over a perimeter edge of the implant. The implant may also include indentations such as grooves to promote articular cartilage remodeling over a portion of the load bearing surface of the implant. An elongated or non-round implant is also provided having two opposing concentric arcuate shaped sides, as well as a method to seat such an implant in an articular surface. A method for seating an implant without cutting articular cartilage is also provided. | 03-18-2010 |
20100076563 | OPERATIVELY TUNING IMPLANTS FOR INCREASED PERFORMANCE - A method for preoperatively characterizing an individual patient's biomechanic function in preparation of implanting a prosthesis is provided. The method includes subjecting a patient to various activities, recording relative positions of anatomy during said various activities, measuring force environments responsive to said patient's anatomy and affected area during said various activities, characterizing the patient's biomechanic function from said relative positions and corresponding force environments, inputting the measured force environments, relative positions of knee anatomy, and patient's biomechanic function characterization into one or more computer simulation models, inputting a computer model of the prosthesis into said one or more computer simulation models, and manipulating the placement of the prosthesis in the computer simulation using said patient's biomechanic function characterization and said computer model of the prosthesis to approximate a preferred biomechanical fit of the prosthesis. | 03-25-2010 |
20100076564 | Tibial tuberosity advancement implant - A tibial tuberosity advancement implant with first and second arms pivotally joined at an apex. Tabs including anchor apertures extend from each arm for attachment of the arms in a traverse osteotomyized tibia. A selection of various width keys are each insertable between the arms for setting the distance between the arms and the width of the osteotomyized tibia. | 03-25-2010 |
20100087929 | SHAPED PART OF AN ULTRA HIGH MOLECULAR WEIGHT POLYETHYLENE - Shaped parts of ultra high molecular weight polyethylene (UHMWPE) are made by a process comprising melt processing, wherein a) the UHMWPE has a weight average molecular weight (Mw) of at least 1*106 g/mol, b) during the shaping the storage plateau modulus of the UHMWPE (G*) is kept at a value of at most 1.5 MPa, c) whereafter, before the cooling, the G* is raised to its final value. The shaped parts may advantageously be used in medical applications, e.g., as an element of a hip or knee prosthesis. | 04-08-2010 |
20100094429 | PROSTHETIC DEVICE FOR KNEE JOINT AND METHODS OF IMPLANTING AND REMOVING SAME - A prosthetic device for a knee joint includes a body portion and a first keel. The body portion attaches to a bone of a knee joint. The body portion can have a bearing surface configured to replace at least a portion of the bone and an implantation surface configured to face the bone upon implantation. The first keel can be configured to be inserted into a corresponding first keel void formed in the bone. The first feel can be configured to project outwardly from the implantation surface by an amount sufficient to inhibit movement of the body portion relative to the bone in both medial and lateral directions upon insertion into the first keel void. The first keel can extend along a longitudinal direction of the body portion and is offset from a longitudinal centerline of the body portion. Methods of implanting and removing the prosthetic device are also provided. | 04-15-2010 |
20100100189 | HIGH FLEXION TIBIAL TRAY - Various assemblies for replacing at least a proximal portion of a tibia are provided. One assembly includes a tibial tray including a superior bearing engaging surface and an inferior bone engaging surface and having a truncated posterior region; a bearing including an articulating surface, a tray mating surface, and an overhang. The tray mating surface of the bearing is in mating engagement with the inferior bone engaging surface of the tibial tray such that the overhang of the bearing extend beyond the tibial tray truncated posterior region. Related surgical methods are also provided. | 04-22-2010 |
20100100190 | TIBIAL TRAY HAVING A REINFORCING MEMBER - A knee joint prosthesis can include a tibial component that can have a tibial tray. The tibial tray can include a platform-like tray that defines a superior surface and an inferior surface. The platform-like tray can have a tray perimeter and a raised wall formed on the inferior surface. The raised wall can be offset inboard relative to the tray perimeter. Porous material can be disposed on the inferior surface of the platform-like tray at a location generally between the raised wall and the tray perimeter. | 04-22-2010 |
20100114322 | Extra-Articular Implantable Mechanical Energy Absorbing Systems and Implantation Method - A system and method for sharing and absorbing energy between body parts. In one aspect, the method involves identifying link pivot locations, fixing base components and minimally invasive insertion techniques. In one particular aspect, the system facilitates absorbing energy between members forming a joint such as between articulating bones. | 05-06-2010 |
20100174377 | RETICULATED PARTICLE POROUS COATING FOR MEDICAL IMPLANT USE - A composition, a medical implant constructed from the composition, and a method of making the composition are described. The composition comprises a porous-coated substrate, the porous coating comprising a reticulated particle coating, the coating being formed by fusing the reticulated particle to the surface, preferably by sintering. | 07-08-2010 |
20100217400 | PROSTHETIC DEVICE, METHOD OF PLANNING BONE REMOVAL FOR IMPLANTATION OF PROSTHETIC DEVICE, AND ROBOTIC SYSTEM - A prosthetic device, method for planning bone removal, and a robotic system for implantation of a prosthetic device in bone are disclosed. The prosthetic device can include a body portion for attachment to a bone, wherein the body portion includes an implantation surface configured to face the bone upon implantation, and a constraint structure. The prosthetic device, method, and robotic system can be configured to cause the constraint structure and bone to interact so as to constrain the prosthetic device in the bone. | 08-26-2010 |
20100222888 | Prosthetic Devices - A prosthetic device made of a first specific type of polyarylene, taken alone or in combination with a second specific type of polyarylene, featuring some unexpected advantages such as a very high strength and stiffness, good elongation properties, high chemical resistance, good biocompatibility as well as an outstanding impact resistance. | 09-02-2010 |
20100249939 | TRAPEZOIDAL BONE PLUGS AND METHOD OF BONE-TENDON-BONE ACL RECONSTRUCTION - A method of synthetic grafting of bone-tendon-bone autograft harvest sites using preformed synthetic trapezoidal implants. The implants are formed of tricalcium phosphate, an osteoconductive bone graft substitute and filler, which allows for simultaneous controlled absorption and promotion of osteogenesis. The implants are preferably pretreated or presoaked intraoperatively in autologous blood, or autologous conditioned plasma, or bone marrow aspirate products to enhance healing ability. The implants are trimmed to match the patellar pole shape, pressed into place in the bone voids, and oversewn to complete the procedure. | 09-30-2010 |
20100268347 | MICRO AND NANO SCALE SURFACE TEXTURED TITANIUM-CONTAINING ARTICLES AND METHODS OF PRODUCING SAME - The present invention relates to processes involving contacting articles that include titanium or titanium alloy with a solution comprising hydrochloric acid and chloride-containing compound for a time and at a temperature effective to form a plurality of indentions that, independently, have a diameter of from about 200 nm to 10 microns. | 10-21-2010 |
20100292803 | COMPOSITIONS AND METHODS FOR FORMING AND CLINICALLY UTILIZING ARTICULATING SPACING DEVICES - The present invention provides molds and methods for producing articulating spacers that are custom-fit to the bone and can be used in two-stage revision knee arthroplasty and other orthopaedic surgery. | 11-18-2010 |
20100292804 | SYSTEMS AND METHODS FOR PROVIDING DEEPER KNEE FLEXION CAPABILITIES FOR KNEE PROSTHESIS PATIENTS - Systems and methods for providing deeper knee flexion capabilities, more physiologic load bearing and improved patellar tracking for knee prosthesis patients. Such systems and methods include (i) adding more articular surface to the antero-proximal posterior condyles of a femoral component, including methods to achieve that result, (ii) modifications to the internal geometry of the femoral component and the associated femoral bone cuts with methods of implantation, (iii) asymmetrical tibial components that have an unique articular surface that allows for deeper knee flexion than has previously been available, (iv) asymmetrical femoral condyles that result in more physiologic loading of the joint and improved patellar tracking and (v) modifying an articulation surface of the tibial component to include an articulation feature whereby the articulation pathway of the femoral component is directed or guided by articulation feature. | 11-18-2010 |
20110035017 | PROSTHESIS WITH CUT-OFF PEGS AND SURGICAL METHOD - A joint prosthesis system has two metal implant components and a bearing. One of the metal implant components has an articulation surface for articulation with the bearing. The other metal implant component has a mounting surface for supporting the bearing. An extension extends out from a junction at the bone-engaging surface of one of the metal components to an exposed end. The extension has a thickness at the junction and comprises porous metal across the entire thickness of the extension at the junction. | 02-10-2011 |
20110054625 | Prosthesis Having A Soft Tissue Attachment Element - A prosthetic bone implant, the bone implant forming one side of a joint and including a prosthesis and a soft tissue attachment component. The soft tissue attachment component is connected to the bone implant and extends outwardly therefrom and towards a joint line. The soft tissue attachment component is moveable with respect to the prosthesis while connected thereto. | 03-03-2011 |
20110071642 | Medical implant and knee joint endoprosthesis - The invention relates to a medical implant consisting of a first implant part and a second implant part for the connection of which there is provided a connecting device, wherein at least the first implant part comprises a connecting element receptacle, in which at least one connecting element of the connecting device can be disposed. In order to provide an implant of this type which is easier to handle, it is proposed, in accordance with the invention, that a securing device be provided for the purposes of securing the at least one connecting element in the connecting element receptacle. Moreover, the invention relates to a knee joint endoprosthesis having at least one implant of this type. | 03-24-2011 |
20110093080 | EXTRA-ARTICULAR IMPLANTABLE MECHANICAL ENERGY ABSORBING ASSEMBLIES HAVING TWO DEFLECTING MEMBERS AND METHODS - Implantable assemblies for manipulating energy transferred by members defining an anatomical joint, and methods of implanting and using. The members of the anatomical joint collectively define a path of motion. An assembly includes a first component configured to be attached to a first member of the anatomical joint; a second component configured to be attached to a second member of the anatomical joint; and a joint joining the first and second components. The first component includes a first flex member and the second component includes a second flex member. The first and second flex members are configured to flex to absorb energy transferred by the members of the anatomical joint. | 04-21-2011 |
20110093081 | KNEE BALANCING FOR REVISION PROCEDURES - Methods, systems and devices are provided for facilitating a surgical procedure on a knee, particularly, a revision total knee replacement procedure. Prior femoral and tibial prostheses are removed. A cut end of a distal femur is engaged with a femoral adjustment member, which will typically center itself about an intermedullary rod placed into the femur. The lateral and medial forces exerted by lateral and medial sides of the femoral adjustment member and the cut tibial plateau against each other are measured. The femoral adjustment member is adjusted to apply and/or adjust tension to the lateral collateral ligament and/or the medial collateral ligament based on the measured forces, for example, such that the measured lateral force and the measured medial force are matched. Based on the position of the adjusted femoral member, guided clean-up cuts for placement of a new femoral prostheses are made on the cut end of the distal femur. | 04-21-2011 |
20110093082 | ENHANCED BONDING LAYERS ON TITANIUM MATERIALS - The present invention provides a dense-coverage, adherent phosphorous-based coating on the native oxide surface of a material. Disclosed phosphorous-based coatings include phosphate and organo-phosphonate coatings. The present invention also provides further derivatization of the phosphorous-based coatings to yield dense surface coverage of chemically reactive coatings and osetoblast adhesion-promoting and proliferation-promoting coatings on the native oxide surface of a titanium material. | 04-21-2011 |
20110125277 | DUAL-SIDED JOINT IMPLANT HAVING A WEAR RESISTANT SURFACE AND A BIOACTIVE SURFACE - A medical implant for application in an articulating surface of a joint, comprising a plate-shaped structure having a first surface and a second surface facing mutually opposite directions, the first surface comprising a first biocompatible metal, metal alloy or ceramic and being devised to form a wear resistant articulate surface configured to face the articulating part of the joint; and the second surface comprising a bioactive ceramic or bioactive glass incorporated into a second metal, metal alloy or ceramic and being devised to form a bone contacting surface configured to face bone structure in the joint; wherein: the first surface and the second surface are adhered by means of a sintered material structure. Possibly the second surface is a sintered mixture having a homogenous microstructure comprising the bioactive ceramic or bioactive glass and the second metal, metal alloy or ceramic. | 05-26-2011 |
20110144760 | Patient-Specific and Patient-Engineered Orthopedic Implants - Disclosed herein are methods and devices for repairing a knee joint, including customizable and/or highly selectable implants and/or implant components for each patient to provide optimal fit and function. | 06-16-2011 |
20110202138 | Method and Apparatus for Force Redistribution in Articular Joints - Pathologies of joints arising from improper force distributions are addressed by displacement of targeted connective and muscle tissues surrounding the joint in order to realign force vectors and alter moment arms loading the joint. | 08-18-2011 |
20120035734 | Intracorporeal Component for a Percutaneous Device - An intracorporeal portion of a percutaneous device for a joint disarticulation prosthesis or joint replacement prosthesis, the intracorporeal portion having an extracorporeal portion or having means for rigidly coupling directly to an extracorporeal portion, the extracorporeal portion being for location exterior to the skin, the intracorporeal portion having an articulating component for articulating with an articulating surface, wherein the articulating component is intracorporeal when installed in a human or animal subject. | 02-09-2012 |
20120179265 | KNEE PROSTHESIS - A knee prosthesis for a knee joint with a medial ball-like femoral condyle and with a width “w” is characterized on the lateral compartment by:—a trace-line “Lt | 07-12-2012 |
20120239157 | ULTRA-PASSIVATION OF CHROMIUM CONTAINING ALLOY AND METHODS OF PRODUCING SAME - The invention concerns article having a surface oxide layer up to 20 nm thick, the surface oxide layer comprising chromium and cobalt oxides where the atomic ratio of Cr/Co is more than 3. The invention also concerns methods for treating a chromium containing material, said method comprising contacting said material with a gas plasma under conditions effective to oxidize at least a portion of the material; and contacting said material with an acid. The treated surface is corrosion resistant and can be used in orthopedic implants, especially the wear surface of the orthopedic implant to reduce wear, and other corrosive environment. | 09-20-2012 |
20130024000 | Patient Selectable Joint Arthroplasty Devices and Surgical Tools - Disclosed herein are tools for repairing articular surfaces repair materials and for repairing an articular surface. The surgical tools are designed to be customizable or highly selectable by patient to increase the speed, accuracy and simplicity of performing total or partial arthroplasty. | 01-24-2013 |
20130138218 | SURGICAL METHODS AND INSTRUMENTS FOR IMPLANTING A JOINT UNLOADING SYSTEM - Positioning instruments and related methods are described for implanting an joint unloading system for treating joints. The positioning instruments and methods allow the joint unloading system to be positioned at a joint such that the desired motion will occur for the particular design of a particular joint unloading system which is to be implanted. The positioning instruments include a locating instrument for locating an anatomical feature and a target location for implantation of the joint unloading system, a verification instrument for verification of the target location, an alignment guide, a placement guide for guiding placement of a part of the joint unloading system, and positioning device for aligning portions of the joint unloading system. | 05-30-2013 |
20130204376 | ADJUSTABLE, REMOTE-CONTROLLABLE ORTHOPAEDIC PROSTHESIS AND ASSOCIATED METHOD - An implantable, adjustable prosthesis includes a first component which may be moved relative to a second component by use of a transcutaneous control signal. A method of operating such a prosthesis is also disclosed. | 08-08-2013 |
20130282130 | Prosthesis For Stimulating Natural Kinematics - A bearing component | 10-24-2013 |
20130297031 | PATIENT SPECIFIC INSTRUMENTS AND RELATED METHODS FOR JOINT REPLACEMENT - Devices, tools and techniques for the design, selection and/or modification of patient-specific implants, instruments and related methods are disclosed. Various embodiments include the use of double joint lines, particularly for treating severe deformities during joint repair and/or replacement surgeries. | 11-07-2013 |
20130304219 | SURFACE TREATMENT OF CO-CR BASED ALLOYS USING PLASMA CARBURIZATION - The present invention relates to a method of modifying a surface characteristic (e.g., wear resistance and/or corrosion resistance) of a cobalt-chromium based alloy article. The method comprises plasma treating the article at a temperature in the range of from 300° C. to 700° C. and at a pressure of from 100 Pa to 1500 Pa for 1 hour to 50 hours in an atmosphere comprising at least one carbon-containing gas, whereby to introduce carbon into a surface region of said article. The present invention also resides in a surface-hardened cobalt-chromium based article producible by the method of the invention. The article is characterised by having a surface region comprising a supersaturated solid solution of carbon in cobalt or a surface region comprising a supersaturated solid solution of carbon in cobalt and chromium carbides. Surface hardened articles producible by the method of the invention include medical implants and engineering components. | 11-14-2013 |
20140148910 | OSTEOARTHRITIS TREATMENT AND DEVICE - 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. | 05-29-2014 |
20140236305 | SURGICAL GUIDE FOR IMPLANTING A KNEE PROSTHESIS - The invention relates to a surgical guide ( | 08-21-2014 |
20140277526 | KINETIC ASSESSMENT AND ALIGNMENT OF THE MUSCULAR-SKELETAL SYSTEM AND METHOD THEREFOR - A system is disclosed herein for providing a kinetic assessment and preparation of a prosthetic joint comprising one or more prosthetic components. The system comprises a prosthetic component including sensors and circuitry configured to measure load, position of load, and joint alignment. The system further includes a remote system for receiving, processing, and displaying quantitative measurements from the sensors. The kinetic assessment measures joint alignment under loading that will be similar to that of a final joint installation. The kinetic assessment can use trial or permanent prosthetic components. Furthermore, adjustments can be made to the applied load magnitude, position of load, and joint alignment by various means to fine-tune an installation. The kinetic assessment increases both performance and reliability of the installed joint by reducing error that is introduced by elements that load or modify the joint dynamics not taken into account by prior assessment methods. | 09-18-2014 |
20150148909 | OSTEOARTHRITIS TREATMENT AND DEVICE - 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. | 05-28-2015 |
20150297359 | MEDICAL IMPLANT AND KNEE JOINT ENDOPROSTHESIS - The invention relates to a medical implant consisting of a first implant part and a second implant part for the connection of which there is provided a connecting device, wherein at least the first implant part comprises a connecting element receptacle, in which at least one connecting element of the connecting device can be disposed. In order to provide an implant of this type which is easier to handle, it is proposed, in accordance with the invention, that a securing device be provided for the purposes of securing the at least one connecting element in the connecting element receptacle. Moreover, the invention relates to a knee joint endoprosthesis having at least one implant of this type. | 10-22-2015 |
20160089243 | INJECTION MOULDABLE POLYMERIC COMPOSITE BASED PASSIVE POLYCENTRIC KNEE JOINT - The present invention mainly relates to knee joint and more particularly to the polymeric composite or nanocomposites based polycentric knee joint. In one embodiment the knee joint comprising: a top part having a top face and a bottom face, wherein the top face having an adapter coupled firmly with the top part to transfer the load from the stump of amputee via socket, a bottom part having a top face and a bottom face, at least one middle linkage pivotably coupling a middle posterior region of the top part with a middle posterior region of the bottom part, at least two side identical linkage pivotably coupling a sides of the top part with a sides of the bottom part, a compression spring along with cylindrical rod positioned in the interior of the bottom part which provides the engaging and disengaging of the top and bottom part, at least two extension spring couples the top and bottom part through two tiny holes and through simple supported beam in the top and bottom part for the flexion and extension of the knee joint and a bumper positioned in the base of the bottom part which contacts with the pylon to absorb the vibration and the terminal impact during the hip hike. | 03-31-2016 |
20160192878 | DEVICES, SYSTEMS AND METHODS FOR MONITORING KNEE REPLACEMENTS | 07-07-2016 |
20080255660 | Medical device for treating a heart valve insufficiency - A medical device for treating a heart valve insufficiency, with an endoprosthesis which can be introduced into a patient's body and expanded to secure a heart valve prosthesis in the patient's aorta. In an embodiment, the endoprosthesis has at plurality of positioning arches configured to be positioned with respect to a patient's aorta and a plurality of retaining arches to support a heart valve prosthesis. The endoprosthesis includes a first collapsed mode during the process of introducing it into the patient's body and a second expanded mode when it is implanted. | 10-16-2008 |
20080275550 | Implantable small percutaneous valve and methods of delivery - An implantable prosthetic valve that is transformable from a first helical pre-implantation configuration to a second valvular functional configuration, and methods of delivery. | 11-06-2008 |
20090030512 | Circulatory valve, system and method - Apparatuses, systems, and methods for use in a vascular system. The apparatus include a circulatory valve having a valve frame in which frame members define frame cells. Frame cells include joints in opposing relationship, where the joints transition from a first stable equilibrium state through an unstable equilibrium state to a second stable equilibrium state as the joints are drawn towards each other. | 01-29-2009 |
20090132035 | Prosthetic Heart Valves, Support Structures and Systems and Methods for Implanting the Same - Prosthetic valves and their component parts are described, as are prosthetic valve delivery devices and methods for their use. The prosthetic valves are particularly adapted for use in percutaneous aortic valve replacement procedures. The delivery devices may be adapted for use in minimally invasive or endovascular surgical procedures. | 05-21-2009 |
20090276039 | Implantable Prosthetic Valve - An implantable prosthetic valve for regulating fluid flow through a body vessel is provided. The prosthetic valve comprises an anchoring member, at least one leaflet, and a restraining member capable of temporarily preventing substantial movement of the leaflet between and open and closed position so as to allow fluid flow in the antegrade and retrograde directions. In various embodiments, the prosthetic valve reduces the risk of thrombosis. In various embodiments, the prosthetic valve reduces the appearance of potentially thrombogenic abnormal flow patterns at the site of implantation immediately following the implantation, allows cell deposition making the valve more biocompatible, less thrombogenic before flow changes resulting from valving action set in and allows tissue growth so that a partially or completely biological functioning valve may form on the scaffold provided by the implant. | 11-05-2009 |
20100023119 | Valve Mold and Prosthesis for Mammalian Systems - A valve mold for a prosthetic valved conduit includes two thin film transparent plastic templates having the molding shape of the valve to sandwich biological tissue membrane to form the valve. In another embodiment, a valve mold template has a 3-dimensional geometry which, when folded and sutured to form a close-loop, resembles the geometry of a native aortic valve. The attachment side of a template designed in accordance with the principles of the invention may have a slightly undulating edge, according to one embodiment. | 01-28-2010 |
20110022167 | INTRAPARIETAL AORTIC VALVE REINFORCEMENT DEVICE AND A REINFORCED BIOLOGICAL AORTIC VALVE - A reinforcement device for a biological valve includes an arrangement of supports configured to establish a double-trigone geometry in the valve and coupled to a base upon which the valve may be mounted. A plurality of commissural supports establish the geometry of a commissural trigone, and a plurality of intercommissural supports establish the geometry of an intercommissural trigone. A method for reinforcing a biological valve includes using commissural supports in conjunction with intercommissural supports, both sets of supports coupled to a base upon which the valve is mounted. | 01-27-2011 |
20110082540 | Prosthetic Heart Valves, Scaffolding Structures, and Systems and Methods for Implantation of Same - Prosthetic valves and their component parts are described, as are prosthetic valve delivery devices and methods for their use. The prosthetic valves are particularly adapted for use in percutaneous aortic valve replacement procedures. The delivery devices are particularly adapted for use in minimally invasive surgical procedures. | 04-07-2011 |
20110319991 | Low Profile Transcatheter Heart Valve - An implantable prosthetic valve, according to one embodiment, comprises a frame, a leaflet structure, and a skirt member. The frame can have a plurality of axial struts interconnected by a plurality of circumferential struts. The leaflet structure comprises a plurality of leaflets (e.g., three leaflets arrange to form a tricuspid valve). The leaflet structure has a scalloped lower edge portion secured to the frame. The skirt member can be disposed between the leaflet structure and the frame. | 12-29-2011 |
20120035719 | Prosthetic Heart Valves, Support Structures and Systems and Methods for Implanting the Same - Prosthetic valves and their component parts are described, as are prosthetic valve delivery devices and methods for their use. The prosthetic valves are particularly adapted for use in percutaneous aortic valve replacement procedures. The delivery devices are particularly adapted for use in minimally invasive surgical procedures. | 02-09-2012 |
20120089223 | BAR-LESS COMMISSURE ATTACHMENT FOR PROSTHETIC VALVE - An implantable prosthetic valve, according to one embodiment, comprises a radially collapsible and expandable frame and a leaflet structure supported within the frame. The leaflet structure can comprise a plurality of leaflets paired together at commissures. In one embodiment, the commissures can comprise leaflet tabs rolled into spirals around non-rigid reinforcing inserts. In another embodiment, the commissures can comprise a reinforcing sheet folded around leaflet tabs. | 04-12-2012 |
20120095550 | Reinforced Commissural Support Structure - A device and method for controlling commissural tip deflection of a prosthetic valve, thereby both preventing failure due to repeated movement and/or uneven loading of the commissural points and also improving coaptation of the valve leaflets, including connecting reinforcing material between the commissural points so a spring-like span is created across the points. The spanning material may be in the form of a ring that is lashed, sewn or otherwise connected to the commissural points. The reinforcing material may form curved segments between the commissural points that extend outwardly to form sinuses behind the leaflets of the prosthetic valve. The reinforcing material may also extend in an upstream direction to avoid interfering with blood flowing out of the prosthetic valve. | 04-19-2012 |
20120095551 | METHOD FOR IMPLANTING A CARDIOVASCULAR VALVE - A method is provided for implanting a valve having at least one valve leaflet within the cardiovascular system of a subject. One step of the method includes preparing a substantially dehydrated bioprosthetic valve and then providing an expandable support member having oppositely disposed first and second ends and a main body portion extending between the ends. Next, the substantially dehydrated bioprosthetic valve is attached to the expandable support member so that the substantially dehydrated bioprosthetic valve is operably secured within the main body portion of the expandable support member. The expandable support member is then crimped into a compressed configuration and placed at a desired location within the cardiovascular system of the subject. Either before or after placement at the desired location, fluid or blood re-hydrates the substantially dehydrated bioprosthetic valve. | 04-19-2012 |
20130023984 | COMMISSURE MODIFICATION OF PROSTHETIC HEART VALVE FRAME FOR IMPROVED LEAFLET ATTACHMENT - Embodiments of the present disclosure provide an improved support frame for a prosthetic heart valve. The support frame can include a plurality of diamond-shaped cells arranged in a plurality of circumferential rows. Three cells corresponding to the leaflet commissures can be configured as commissure tip cells, with elongated rounded portions rather than a diamond shape. The commissure tip cells can allow for insertion of leaflet tabs, thereby allowing the leaflets to be sutured outside of the valve. In this manner, the leaflet sutures can be removed from areas of high stress during physiologic loading. Thus, currently disclosed embodiments of a support frame can allow for use of thinner leaflet materials than possible with conventional prosthetic heart valves, without sacrificing valve durability in some embodiments. | 01-24-2013 |
20130046378 | Stented Prosthetic Heart Valves - A surgical sutureless valve that is attached to a stent frame for delivery to a location in a patient using percutaneous implantation devices and methods. | 02-21-2013 |
20130066419 | HEART VALVE REPLACEMENT - A prosthetic heart valve includes a radially expandable stent and a plurality of leaflets. Each leaflet includes a coaptation portion, an arcuate edge, and a belly. The coaptation portion is movable relative to respective coaptation portions of the other leaflets. The acuate edge has a first end and a second end and is coupled to the stent. The belly extends from the arcuate edge to an axis defined by the first and second ends of the arcuate edge, wherein the ratio of the surface area of the belly to the outer cross-sectional area of the expanded stent is about 0.09 to about 0.16. | 03-14-2013 |
20130144382 | TRANSCATHETER VALVE HAVING REDUCED SEAM EXPOSURE - A transcatheter valve having an expandable frame and a collapsible multi-portion skirt within the frame are provided with seams between the portions of the skirt that are located to cooperate with features of the frame and thereby reduce the exposure of the seams. | 06-06-2013 |
20130150956 | PROSTHETIC HEART VALVE HAVING IMPROVED COMMISSURE SUPPORTS - A prosthetic heart valve according to the present disclosure comprises a radially collapsible and expandable annular frame and a leaflet structure comprising a plurality of leaflets mounted within the frame. The frame in particular embodiments can have commissure attachment portions that are configured to support the commissures of the leaflets at locations spaced radially inwardly toward the longitudinal flow axis of the prosthetic valve relative to the frame portions circumscribing the moveable portions of the leaflets. When the leaflets open under pressure of blood flowing through the prosthetic valve, the moveable portions of the leaflets are retained at positions spaced inwardly from the inner surface of the frame to protect against abrasion of the leaflets. | 06-13-2013 |
20130204358 | Prosthetic Tissue Valve - A prosthetic tissue valve for aortic, pulmonary, mitral or tricuspid valve replacement is described herein. A sewing ring for use with the prosthetic tissue valve is also described. The valve can have a circumference that is a predetermined distance larger than the circumference of an annulus in a defective valve. The valve can be substantially planar in an unstressed position before attachment at the annulus and substantially non-planar upon attachment in a biased position at the annulus. Methods are provided for placing the valve as described herein in the biased position within the annulus of the defective valve. | 08-08-2013 |
20140046436 | IMPLANTABLE PROSTHETIC VALVES AND METHODS - A prosthetic valve including an annulus, a pair of leaflets, and a pair of support elements is described. The annulus has a generally saddle-type shape and is connected to the support elements. The pair of leaflets extends from the annulus and are separated from each other by the support elements. In use, the valve is open when the support elements are angled or separated outward, and sealed or closed when the support elements are angled or moved inward. | 02-13-2014 |
20140194978 | Transcatheter Heart Valves - A prosthetic heart valve comprises a biological tissue valve and a collapsible and expandable support frame comprising longitudinal axis. The frame comprises an outflow circumferential structure defining an outflow end of the frame and defining a single row of expandable cells, and a circumferential undulating strut structure spaced apart from the outflow circumferential structure. The frame also comprises three struts longitudinally aligned with the longitudinal axis, configured to facilitate mounting the biological tissue valve to the frame, and interconnecting the outflow circumferential structure to the circumferential undulating structure. Each strut comprises a first end terminating at a respective junction between two adjacent expandable cells of the outflow circumferential structure, and a second end terminating at the circumferential undulating strut structure. The prosthetic heart valve is configured to be collapsed for introduction into a patient using a catheter and to be expanded for deployment at an implantation site. | 07-10-2014 |
20140194979 | Transcatheter Heart Valves - A prosthetic heart valve comprises a collapsible and expandable support frame comprising a longitudinal axis. The frame comprises a first circumferential undulating structure defining an outflow end of the frame, and a second circumferential undulating structure spaced apart from the first circumferential undulating structure. The frame also comprises a plurality of struts longitudinally aligned with the longitudinal axis of the frame, and connecting: the first circumferential undulating structure to the second circumferential undulating structure. Each strut of the plurality of struts comprises a first end terminating at a trough of the first circumferential undulating structure, and a second end terminating at a peak of the second circumferential undulating structure. The prosthetic heat valve also comprises a biological tissue valve coupled to the frame. The prosthetic heart valve is configured to be collapsed for introduction into a patient using a catheter and to be expanded for deployment at an implantation site. | 07-10-2014 |
20140194980 | Reinforced Commissural Support Structure - A device and method for controlling commissural tip deflection of a prosthetic valve, thereby both preventing failure due to repeated movement and/or uneven loading of the commissural points and also improving coaptation of the valve leaflets, including connecting reinforcing material between the commissural points so a spring-like span is created across the points. The spanning material may be in the form of a ring that is lashed, sewn or otherwise connected to the commissural points. The reinforcing material may form curved segments between the commissural points that extend outwardly to form sinuses behind the leaflets of the prosthetic valve. The reinforcing material may also extend in an upstream direction to avoid interfering with blood flowing out of the prosthetic valve. | 07-10-2014 |
20140214158 | SURGICAL HEART VALVE FLEXIBLE STENT FRAME STIFFENER - A prosthetic heart valve includes an annular frame having annularly spaced commissure portions and an annulus portion disposed near an inflow edge, a fabric covering at least a portion of the frame and a valve assembly connected to the frame at the commissure portions, the valve assembly including a plurality of leaflets. A stiffening member is disposed about the frame to limit ovalization of the frame when a radial force is applied to the frame. | 07-31-2014 |
20140214159 | PROSTHETIC VALVES AND RELATED INVENTIONS - This invention relates to the design and function of a compressible valve replacement prosthesis, collared or uncollared, which can be deployed into a beating heart without extracorporeal circulation using a transcatheter delivery system. The design as discussed focuses on the deployment of a device via a minimally invasive fashion and by way of example considers a minimally invasive surgical procedure preferably utilizing the intercostal or subxyphoid space for valve introduction. In order to accomplish this, the valve is formed in such a manner that it can be compressed to fit within a delivery system and secondarily ejected from the delivery system into the annulus of a target valve such as a mitral valve or tricuspid valve. | 07-31-2014 |
20140222140 | METHODS OF IMPLANTING MINIMALLY-INVASIVE PROSTHETIC HEART VALVES - Expandable prosthetic heart valves for minimally invasive valve replacement are disclosed. In one preferred embodiment, an expandable prosthetic heart valve includes a support stent comprising an expandable tubular base along an inflow end and three upstanding commissure posts along an outflow end. The three commissure posts are spaced at 120 degree intervals with gaps therebetween. The prosthetic heart valve further includes a tubular flexible member having a prosthetic section and a fabric section. The prosthetic section is connected to the three commissure posts and defines three leaflets, preferably formed of pericardial tissue. The fabric section is sutured to the expandable tubular base. The tubular base may be formed with a shape memory material and is sized for deployment with an annulus of a native aortic valve. After deployment, the three commissure posts support the leaflets above the tubular base for replacing the function of the native aortic valve. In one variation, flanges may be provided on the support stent for improving attachment of the support stent to the host tissue. | 08-07-2014 |
20140222141 | PROSTHETIC MITRAL VALVE - A prosthetic mitral valve with a compressible and expandable stent that, when expanded, is circumferentially oval, elliptical, or D-shaped, with a major axis and a minor axis ratio of from about 3:4 to about 4:5. Embodiments of the stent comprise three commissure posts disposed towards an outflow end and three curved cusp regions between adjacent commissure posts. Three flexible leaflets are attached to the commissure posts in a tri-foil configuration. Embodiments of the prosthetic mitral valve include an atrial ring disposed at the inflow end of the stent. | 08-07-2014 |
20140236288 | Valve prostheses - The present invention discloses devices and methods for performing intravascular procedures without cardiac bypass. The devices include various embodiments of temporary filter devices, temporary valves, and prosthetic valves. | 08-21-2014 |
20140257473 | METHODS FOR INHIBITING STENOSIS, OBSTRUCTION, OR CALCIFICATION OF A STENTED HEART VALVE OR BIOPROSTHESIS - The present invention relates to methods for inhibiting stenosis, obstruction, or calcification of a valve following implantation of a valve prosthesis which may involve disposing a coating composition on an elastical stent or valve leaflet. The valve prosthesis is mounted on the elastical stent such that the elastical stent is in contact with the valve. | 09-11-2014 |
20140330369 | Prosthetic Tissue Valves and Methods for Anchoring Same to Cardiovascular Structures - A prosthetic atrioventricular tissue valve comprising a continuous tubular member formed from a first biocompatible material, the tubular member having proximal and distal ends, and at least one valve leaflet formed therein, the distal end of the tubular member including cardiovascular structure engagement means for connecting the tubular member to a cardiovascular structure, the cardiovascular structure engagement means comprising a plurality of elongated members that extend distally from the distal end of the tubular member. | 11-06-2014 |
20140330370 | Prosthetic Valve Delivery and Mounting Apparatus and System - A valve mounting apparatus having an elongated tubular mesh structure with proximal and distal ends, a cardiovascular structure engagement region disposed between the proximal and distal ends, and a lumen therethrough, the distal end of the structure including a valve engagement region that is configured to engage a first end of a prosthetic valve, the mesh structure being configured to transition from a pre-deployment configuration, wherein the structure is capable of being disposed at a cardiovascular valve region, such as a valve annulus region, to a post-deployment expanded configuration, wherein the cardiovascular structure engagement region is anchored to the cardiovascular valve region. | 11-06-2014 |
20140358224 | SIX CELL INNER STENT DEVICE FOR PROSTHETIC MITRAL VALVES - This invention relates to a self-expanding wire frame for a pre-configured compressible transcatheter prosthetic cardiovascular valve, a combined inner valve-outer collar component system, and methods for deploying such a valve for treatment of a patient in need thereof. | 12-04-2014 |
20150025625 | CARDIAC REPAIR PROSTHESIS SETS AND METHODS - Cardiac repair prostheses, sets, and methods for implanting in an aorta are disclosed. Cardiac repair prosthesis sets can include a radially expandable support supporting a unidirectional valve that is configured for implantation into the aortic valve region of a patient and a second radially expandable support for a substantially blood impervious stent having a size and shape for implantation into the ascending aorta of said patient where the unidirectional valve and stent are configured for integration within the patient by at least one joining element. Cardiac repair prostheses can include a radially expandable support supporting a unidirectional valve configured for implantation into the aortic valve region of a patient and a second radially expandable support for a substantially blood impervious stent having a size and shape for implantation into the ascending aorta of said patient where the unidirectional valve and stent are joined by at least one joining element. | 01-22-2015 |
20150081012 | MESH ENCLOSED TISSUE CONSTRUCTS - A scaffold to form tissue membranes, comprising: at least one layer of mesh having a first side and a second side, the layer of mesh being either a woven wire metal mesh or a flat metal sheet that is acid-etched such that the layer of mesh includes a network of holes passing directly through the mesh from the first side to the second side; and at least one layer of cells at each side of the mesh enclosing the layer of mesh, such that the at least one layer of cells on the first side interacts with the at least one layer of cells on the second side through the network of holes to provide for structure integration. | 03-19-2015 |
20150127095 | Heart Valve Prosthesis and Methods of Manufacture and Use - A heart valve prosthesis is provided having a self-expanding multi-level frame that supports a valve body comprising a skirt and plurality of coapting leaflets. The frame transitions between a contracted delivery configuration that enables percutaneous transluminal delivery, and an expanded deployed configuration having an asymmetric hourglass shape. The valve body skirt and leaflets are constructed so that the center of coaptation may be selected to reduce horizontal forces applied to the commissures of the valve, and to efficiently distribute and transmit forces along the leaflets and to the frame. Alternatively, the valve body may be used as a surgically implantable replacement valve prosthesis. | 05-07-2015 |
20150127096 | METHOD FOR REPLACING MITRAL VALVE - A method of implanting a prosthetic mitral valve assembly using a transapical procedure is disclosed. An incision is formed in the chest in the apex of the patient's heart. A delivery catheter containing the prosthetic mitral valve assembly is advanced over a guidewire into the patient's heart. The prosthetic mitral valve assembly is deployed from the delivery catheter into the native mitral valve. The prosthetic mitral valve assembly comprises a stent having a lower portion for placement between the leaflets of a native mitral valve and an upper portion having a flared end for placement above the annulus. The prosthetic mitral valve includes a valve portion having leaflets formed of pericardial tissue. A plurality of upwardly bent prongs are provided along an outer surface of the stent for preventing upward migration of the prosthetic mitral valve assembly after deployment. | 05-07-2015 |
20150289974 | Reinforced Prosthetic Tissue Valves - A prosthetic atrioventricular valve that includes a continuous tubular member having proximal and distal ends, the tubular member comprising an extracellular matrix (ECM) material, and a reinforcement member disposed in the tubular member lumen and attached to the distal end of the tubular member, the reinforcement member comprising at least two elongated linear members that are configured to connect the joined tubular and reinforcement members to a cardiovascular structure. | 10-15-2015 |
20150335422 | PERICARDIAL HEART VALVE REPLACEMENT AND METHODS OF CONSTRUCTING THE SAME - The pericardial heart valve replacement ( | 11-26-2015 |
20160374802 | PROSTHETIC HEART VALVE - Embodiments of a radially collapsible and expandable prosthetic heart valve are disclosed. A valve frame can have a tapered profile when mounted on a delivery shaft, with an inflow end portion having a smaller diameter than an outflow end portion. The valve can comprise generally V-shaped leaflets, reducing material within the inflow end of the frame. An outer skirt can be secured to the outside of the inflow end portion of the frame, the outer skirt having longitudinal slack when the valve is expanded and lying flat against the frame when the valve is collapsed. A diagonally woven inner skirt can elongate axially with the frame. Side tabs of adjacent leaflets can extend through and be secured to window frame portions of the frame to form commissures. The window frame portions can be depressed radially inward relative to surrounding frame portions when the valve is crimped onto a delivery shaft. | 12-29-2016 |
623200150 | Trileaflet | 11 |
20080312737 | Mono Cusped Patch and Valved Conduit for Repairing Cardiac Outflow Tract - A mono cusped patch for repairing cardiac outflow tract is disclosed in the present invention, which comprises an inner patch, an external supporting patch and a leaflet. An approximate semicircular slit is provided on the inner patch. The inferior border of the leaflet is set between the inner patch and the external supporting patch along the slit. The inner patch, the inferior border of the leaflet and the external supporting patch are stitched together along the slit edge of the inner patch with sutures. The inferior border of the leaflet is fixed between the inner patch and the external supporting patch. According to this special stitching structure, the present invention also provides a valved conduit of good performance. The leaflets of mono cusped patch and valved conduit are sutured with the inner patch/conduit and external supporting patch/conduit to repair cardiac outflow tract, and the inferior border of leaflet is provided between the inner patch/conduit and external supporting patch/conduit, so that the present invention avoids fixing leaflet only with sutures, makes leaflets more durable and improves postoperative longtime treatment effect of patients significantly. | 12-18-2008 |
20120165928 | DEVICES FOR REDUCING LEFT ATRIAL PRESSURE, AND METHODS OF MAKING AND USING SAME - A device for regulating blood pressure between a patient's left atrium and right atrium comprises an hourglass-shaped stent comprising a neck region and first and second flared end regions, the neck region disposed between the first and second end regions and configured to engage the fossa ovalis of the patient's atrial septum; and a one-way tissue valve coupled to the first flared end region and configured to shunt blood from the left atrium to the right atrium when blood pressure in the left atrium exceeds blood pressure in the right atrium. The inventive devices may reduce left atrial pressure and left ventricular end diastolic pressure, and may increase cardiac output, increase ejection fraction, relieve pulmonary congestion, and lower pulmonary artery pressure, among other benefits. The inventive devices may be used, for example, to treat subjects having heart failure, pulmonary congestion, or myocardial infarction, among other pathologies. | 06-28-2012 |
20120259409 | Heart Valve Prosthesis and Methods of Manufacture and Use - A heart valve prosthesis is provided having a self-expanding multi-level frame that supports a valve body comprising a skirt and plurality of coapting leaflets. The frame transitions between a contracted delivery configuration that enables percutaneous transluminal delivery, and an expanded deployed configuration having an asymmetric hourglass shape. The valve body skirt and leaflets are constructed so that the center of coaptation may be selected to reduce horizontal forces applied to the commissures of the valve, and to efficiently distribute and transmit forces along the leaflets and to the frame. Alternatively, the valve body may be used as a surgically implantable replacement valve prosthesis. | 10-11-2012 |
20120303117 | EXTRACELLULAR MATRIX MATERIAL CONDUITS AND METHODS OF MAKING AND USING SAME - Extracellular matrix (ECM) material conduits are disclosed. Methods for regenerating atrioventricular valves to replace defective atrioventricular valves within a heart of a subject using the ECM material conduits are also disclosed. Methods of sterilizing and decellularizing an ECM material are also disclosed. | 11-29-2012 |
20120310335 | EXTRACELLULAR MATRIX MATERIAL VALVE CONDUIT AND METHODS OF MAKING THEREOF - Methods for forming extracellular matrix valve conduits are disclosed. Extracellular matrix valve conduits produced using the disclosed methods are also disclosed. Methods of sterilizing and decellularizing extracellular matrix materials are also disclosed. | 12-06-2012 |
20130150957 | DECALCIFYING HEART VALVE - Vascular valve systems for treating calcified vascular vessel valves by delivery of one or more calcium chelating agents are described. Methods of making the vascular valve systems are also described. | 06-13-2013 |
20140058503 | ARTIFICIAL VALVE LEAFLET - An artificial mitral valve has a ring, an anterior cusp-side region, a posterior cusp-side region and a valve leaflet connected along an outer edge of the ring. The valve leaflet includes an anterior cusp forming member connected to the anterior cusp-side region and a posterior cusp forming member connected to the posterior cusp-side region. The anterior cusp forming member is provided with has an upper edge joined to the ring and a lower edge that forms a bifurcated portion. The upper edge is made up of a pair of right and left edges that incline inward and upward from the right and left sides, and a curved edge interposed between the inclined edges that curves along the anterior cusp-side region. The posterior cusp forming member has an upper edge joined to the ring and a lower edge that forms a bifurcated portion. | 02-27-2014 |
20140277416 | Seamless Tubular Extracellular Matrix Prosthetic Valve and Method for Forming Same - A seamless prosthetic valve comprising a continuous tubular member having an outer abluminal surface, a triple walled intermediate portion, and at least a first valve leaflet that is configured to selectively restrict fluid flow through the valve, the triple walled intermediate portion being formed by everting a first end of member over the member, whereby a double walled end is formed, and reverting the first end over the double walled end of the member, the first valve leaflet being formed by suturing the triple walled intermediate portion at a first commissure connection point. | 09-18-2014 |
20150032205 | Seamless Tubular Extracellular Matrix Prosthetic Valve and Method for Forming Same - A seamless prosthetic valve having an outer abluminal surface, a triple walled intermediate portion, and at least one valve leaflet that is configured to selectively restrict fluid flow through the valve, the valve leaflet being formed by suturing the triple walled intermediate portion at a first commissure connection point. | 01-29-2015 |
20160000559 | HEART VALVE PROSTHESIS | 01-07-2016 |
20160074162 | COLLAPSIBLE PROSTHETIC HEART VALVES - Prosthetic heart valves, which are collapsible to a relatively small circumferential size for less invasive delivery into a patient and which then re-expand to operating size at an implant site in the patient, include a collapsible/expandable stent-like supporting structure and various components of flexible, sheet-like material that are attached to the supporting structure. For example, these sheet-like other components may include prosthetic valve leaflets, layers of buffering material, cuff material, etc. Improved structures and techniques are provided for securing such other components to the stent-like supporting structure of the valve. | 03-17-2016 |
20080275560 | FEMORAL AND TIBIAL BASE COMPONENTS - Various embodiments are directed to base components that are usable with implantable mechanical energy absorbing systems. According to one embodiment, the base component includes a low-profile body having a elongate, straight portion at a first end and a curved body portion at a second end. The second end is elevated as compared to the first end. An inner surface of the low-profile body has a raised portion extending along the elongate, straight portion of the low-profile body. The base component also includes a plurality of openings positioned along the low-profile body for alignment and purposes of affixation to body anatomy. | 11-06-2008 |
20080306603 | Modular implant part and knee joint prosthesis - In order to improve a modular implant part for replacing a part of a natural knee joint with an implant component comprising a shaft extending away from the implant component and a connecting device for connecting the shaft to the implant component such that the shaft is adapted to be fixed to the implant component in a multiplicity of desired positions in a simple manner, it is proposed that the connecting device be formed in such a manner that, in a mounting disposition, the shaft is adapted to be moved into different translatory positions by a translatory movement in a direction transverse or substantially transverse to its longitudinal axis, and that, in an implantation disposition, the shaft is adapted to be fixed immovably to the implant component in one of the different translatory positions. Furthermore, an improved knee joint prosthesis is proposed. | 12-11-2008 |
20090149963 | PROSTHESIS ASSEMBLY INCLUDING ANGLE AND POSITION ADAPTORS - A modular prosthesis assembly for insertion in bone, the assembly comprising: a tray element having a first surface including an extension member depending therefrom and an opposite second surface; a first adaptor having first and second ends, the first end having a profile part which receives and retains the extension member; a second adaptor comprising, a first end and a second end; the first end engagable with the second end of the first adaptor; a stem having first and second end, the first end including a formation which allows engagement of the stem with the second end of the second adaptor. The second end of said stem has a profile suitable for insertion in bone. | 06-11-2009 |
20090149964 | KNEE JOINT PROSTHESIS SYSTEM AND METHOD FOR IMPLANTATION - A method for preparing at least a first bone for receiving a prosthesis can include positioning an IM member in a bone. A scaffold, skeleton or frame can be located onto the bone at a desired location. An alignment assembly can be coupled to the frame. The alignment assembly can be moved relative to the IM member to position the frame at a desired location relative to the bone. The frame can be fixed to the bone at the desired location. A cavity can be reamed into the bone using at least a portion of the alignment assembly as a guide. The alignment assembly can be removed from the frame. A cutting block can be coupled to the first attachment portion. Cuts can be prepared in the bone using the cutting block as a guide. | 06-11-2009 |
20090265011 | Femoral component of an artificial knee joint - A femoral component of an artificial knee joint is configured with multiple different facets which are similar in size and shape for many different sizes, to simplify an associated method for forming a distal end of the femur to receive the femoral component. Jig embodiments are provided to form surfaces on a distal end of a femur to correspond with facets of the femoral component, with the same jig usable for femoral components of differing size. The femoral component includes medial and lateral condylar legs with a posterior facet of the femoral component exhibiting a negative angle relative to a central axis of the femur, to maximize contact and increase flexion of the artificial knee joint. | 10-22-2009 |
20090319047 | RECESS-RAMP KNEE JOINT PROSTHESIS - A recess-ramp knee joint prosthesis comprising a femoral and a tibial component is configured to reproduce normal kinematics and function. Asymmetric condular surfaces and a cupola of the femoral component interact with corresponding dished surfaces and a ramp of the tibia thereby duplicating the behavior of the anatomical knee. | 12-24-2009 |
20110015749 | MODULAR APPARATUS AND METHOD FOR SCULPTING THE SURFACE OF A JOINT - The present invention provides a modular device for restoring individual joint kinematics using minimally invasive surgical procedures. The modular implants include distinct components that include tethering means. The modular implants provide intraoperative surgical options for articular constraint and facilitate proper alignment and orientation of the joint to restore kinematics as defined by the individual patient anatomy. | 01-20-2011 |
20110112650 | MODIFIED MODULAR JOINT PROSTHESIS COMPONENT - A modified joint prosthesis component is provided to reduce the backside wear of the joint implant. Whether the joint implant is for the knee joint, the hip joint or another joint, it is the modified bearing insert engaging surface of the metal base construct that provides for greater friction and therefore less micro-motion and resultant minimized backside wear. | 05-12-2011 |
20110112651 | FEMORAL AUGMENTS FOR USE WITH KNEE JOINT PROSTHESIS - A femoral augment, or set of augments, for use with a knee joint prosthesis, where the femoral augment includes a main body portion, an aperture formed within the main body portion and extending in a generally distal/proximal direction, and a pair of legs extending outwardly from said main body portion in a generally posterior direction. In the preferred embodiment, the aperture is configured to receive a stem extension implant, and to allow it to pass through. Additionally, the legs of the femoral augment are preferably configured to be seated proximal of a proximal side of a pair of condylar portions of a femoral component of a knee joint prosthesis. The present invention is intended for situations in which the distal portion of the femur is defective, and it provides a method and devices that allow for preservation of healthy peripheral bone, while still providing the necessary augmentation to the distal portion of the femur. | 05-12-2011 |
20110178605 | KNEE PROSTHESIS SYSTEM - A knee prosthesis system for total knee replacement procedures includes a plurality of distinctly-sized femoral components, a plurality of distinctly-sized fixed tibial components, a plurality of distinctly-sized mobile tibial components, a plurality of fixed inserts, and a plurality of mobile inserts. Each of the mobile inserts is sized and shaped such that each may be optimally matched to one of the femoral components and may be used with any one of the mobile tibial components. Each of the fixed inserts is sized and shaped such that each may be optimally matched to one of the femoral components and may be used with any one of the fixed tibial components. | 07-21-2011 |
20110178606 | TIBIAL COMPONENTS FOR A KNEE PROSTHESIS SYSTEM - A knee prosthesis system for total knee replacement of a patient has a plurality of distinctly-sized fixed tibial components, each of which has a fixed platform defining a first, bone covering profile and a plurality of distinctly-sized mobile tibial components, each of which has a mobile platform defining a second, bone covering profile. The first and second, bone covering profiles are approximately the same for any one of the plurality of distinctly-sized fixed tibial components and a correspondingly-sized one of the plurality of distinctly-sized mobile tibial components. | 07-21-2011 |
20110251695 | SYSTEMS AND METHODS FOR TENSIONING LIGAMENTS AND OTHER SOFT TISSUES - Systems, methods and devices for tensioning posterior cruciate ligaments during cruciate or bi-cruciate ligament-sparing arthroplasty. Non-limiting examples of such systems may include at least one series of tibial inserts of equal size; the at least one series of tibial inserts having at least one set of tibial inserts of equal thickness. The at least one set of tibial inserts of equal thickness may include at least two tibial inserts having different geometries in a posterior portion, the different geometries being configured to change the tension in the posterior cruciate ligament (PCL). The different geometries in the posterior portions of the tibial inserts are configured so as to allow the posterior cruciate ligament to be tensioned or loosened independently of the tibial insert thickness and/or size. By providing different posterior geometries for each insert within a set of a series, a surgeon may be provided with more flexibility in choosing an insert that satisfies stability requirements in a non-invasive manner. | 10-13-2011 |
20130013075 | DYNAMIC KNEE BALANCER WITH PRESSURE SENSING - A device for performing a surgical procedure on a knee includes an adjustable femoral portion, a tibial portion and at least one sensor coupled with the femoral and/or tibial portions to sense pressure exerted by the femoral and tibial portions against one another. The femoral portion is adapted for removably coupling with a distal end of a femur to adjust tension in soft tissue adjacent the knee and has at least one positioning feature adapted to move relative to the distal end of the femur as the femoral portion is adjusted, thus helping position a femoral prosthetic on the distal end of the femur. The sensor(s) may be adapted to sense pressure at medial and lateral sides of the knee, and relative pressures may be displayed as data on a visual display. Adjustments to the femoral member may be made to balance pressure at flexion and extension of the knee. | 01-10-2013 |
20130204377 | SYSTEMS AND METHODS FOR PROVIDING A MODULAR FEMORAL COMPONENT - Systems and methods for providing deeper knee flexion capabilities. In some instances, such systems and methods include a modular component, wherein the modular component is configured to attach to a femoral component, and wherein the femoral component is configured to attach to a distal portion of a femur. In some cases, the modular component includes an articular surface that is configured to increase a surface area of an articulation surface of a proximal portion of a posterior condyle of the femoral component. Other implementations are also discussed. | 08-08-2013 |
20130304220 | PROSTHESIS KIT WITH FINNED SLEEVE - A modular prosthesis kit includes a sleeve. The sleeve has a central portion and a fin. At least part of the central portion includes a plurality of adjacent terraces. The fin includes a pair of tapered outer surfaces that are continuous, non-terraced and define a wedge-shape to stabilize the position of the sleeve when implanted. The sleeve may include a single terraced spout or wing with such a fin or may not have any spouts or wings extending out from the central portion. The kit may also include sleeves with two spouts or wings extending out from the central portion. | 11-14-2013 |
20130317620 | SYSTEMS AND METHODS FOR TENSIONING LIGAMENTS AND OTHER SOFT TISSUES - Systems, methods and devices for tensioning posterior crucial ligaments during cruciate or bi-cruciate ligament-sparing arthroplasty. Non-limiting examples of such systems may include at least one series of tibial inserts of equal size; the at least one series of tibial inserts having at least one set of tibial inserts of equal thickness. The at least one set of tibial inserts of equal thickness may include at least two tibial inserts having different geometries in a posterior portion, the different geometries being configured to change the tension in the posterior cruciate ligament (PCL). The different geometries in the posterior portions of the tibial inserts are configured so as to allow the posterior cruciate ligament to be tensioned or loosened independently of the tibial insert thickness and/or size. By providing different posterior geometries for each insert within a set of a series, a surgeon may be provided with more flexibility in choosing an insert that satisfies stability requirements in a non-invasive manner. | 11-28-2013 |
20140005791 | KNEE PROSTHESIS SYSTEM WITH SIDE-MOUNTED AUGMENTS | 01-02-2014 |
20140081408 | FEMORAL KNEE PROSTHESIS SYSTEM WITH AUGMENTS AND MULTIPLE LENGTHS OF SLEEVES SHARING A COMMON GEOMETRY - A modular knee prosthesis system includes a femoral component having a stem, a plurality of different sizes of sleeves mountable on the stem, and a plurality of different sizes of augments mountable on the femoral component. The system is modular, and provides the surgeon with the option of distally offsetting the joint line by selecting the size of sleeve that will provide the desired joint line. The different sizes of sleeves have different axial lengths but share a common geometry along a substantial part of their lengths so that the same bone cavity will accept multiple sizes of sleeves. | 03-20-2014 |
20140081409 | KNEE PROSTHESIS SYSTEM WITH STANDARD AND DISTAL OFFSET JOINT LINE - A modular knee prosthesis system includes a femoral component having a stem and a sleeve. The system is modular, and provides the surgeon with the option of distally offsetting the joint line by controlling the relative axial positions of the stem and the sleeve. Alternative options include providing sleeves with tapered bores of different diameters, providing a shim to be placed between the sleeve and the stem and providing the stems as adapters having different diameters. | 03-20-2014 |
20140081410 | MODULAR KNEE PROSTHESIS SYSTEM WITH MULTIPLE LENGTHS OF SLEEVES SHARING A COMMON GEOMETRY - A modular knee prosthesis system includes a femoral component having a stem and a plurality of different sizes of sleeves mountable on the stem. The system is modular, and provides the surgeon with the option of distally offsetting the joint line by selecting the size of sleeve that will provide the desired joint line. The different sizes of sleeves have different axial lengths but share a common geometry along a substantial part of their lengths so that the same bone cavity will accept multiple sizes of sleeves. | 03-20-2014 |
20140081411 | SURGICAL INSTRUMENT SYSTEM WITH MULTIPLE LENGTHS OF BROACHES SHARING A COMMON GEOMETRY - An orthopaedic surgical instrument system includes a first broach including a first end configured to be separately secured to a handle and a tapered body having a plurality of cutting teeth defined therein, and a second broach including a first end configured to be separately secured to the handle in place of the first broach, a first tapered body extending distally from a second end positioned opposite the first end, and a second tapered body extending distally from the first tapered body. The tapered body of the first broach and the first tapered body of the second broach have a first outer geometry and the second tapered body has a second outer geometry different from the first outer geometry. | 03-20-2014 |
20140180426 | Cannulated Modular Tibial Stem Component Pieces for Use in Total Ankle Arthroplasty and Systems for Installing and Removing Same - An ankle replacement prosthesis comprising a cannulated tibial prosthetic stem component formed by a plurality of cannulated modular stem component pieces and tibial prosthetic instrumentalities and methods for installing the cannulated modular stem component pieces into a distal tibia and removing the cannulated modular stem component pieces from a distal tibia. | 06-26-2014 |
20140207242 | System and Method for Hemi Knee Replacement for Tibial Plateau Fracture - The present invention provides a prosthetic implant for partial replacement of an anatomical part. The implant includes a unitary body with a generally flat lower end face for supporting the body on a cortical surface, a generally curved exterior side face and a generally flat upper end face. A modular bearing plate disposed on the upper end face includes an upper articular surface for supporting articulation of an anatomical surface and an opposed mounting surface in contact with the upper end face. A fixation bracket includes a first end coupled to the exterior side face of the body and a second end projecting downward past the lower end face of the body with a contour generally corresponding to an outer surface of an anatomical part. The prosthetic implant is configured to replace a portion of the outer surface of the anatomical part and extend partially into the anatomical part. | 07-24-2014 |
20140222155 | TAPERED TIBIAL AUGMENT - In typical knee repair or replacement surgery, a femoral implant includes a pair of convex condylar surfaces that can slide within corresponding concave bearing indentations on a tibial bearing surface. The tibial bearing surface is disposed on a proximal side of a tibial platform. A stem can extend distally from the tibial platform, and can attach to a cut proximal end of the tibia. A tibial augment can attach to the distal side of the tibial platform, and can reduce or eliminate a lateral overhang of the tibial platform with respect to the cut proximal end of the tibia. The tibial augment may have a tapered periphery. The taper may extend inward in a distal direction. The taper may vary along the periphery of the tibial augment, so that at least a portion of a medial taper is different from at least a portion of a lateral taper. | 08-07-2014 |
20140277527 | MODULAR KNEE PROSTHESIS SYSTEM FOR USE WITH DIFFERENT LOAD REQUIREMENTS - A modular orthopaedic implant system has first, second and third implant components. Two of the components have bores and the third component has a post. The third component can be assembled with either the first or second components with the post received in the respective bore of the other component. When assembled, the length of the post received within the bore of one of the components is greater than the length of the post received within the bore of the other component. The fatigue strength of the assembly with a greater length of the post received within the bore is greater, and this assembly can be used where such greater fatigue strength is needed and the other assembly can be used where a lesser fatigue strength is needed. Since the third component that is used in both assemblies may be the same, inventory may be reduced. | 09-18-2014 |
20140296989 | SYSTEMS AND METHODS FOR PROVIDING A MODULAR FEMORAL COMPONENT - Systems and methods for providing deeper knee flexion capabilities. In some instances, such systems and methods include a modular component, wherein the modular component is configured to attach to a femoral component, and wherein the femoral component is configured to attach to a distal portion of a femur. In some cases, the modular component includes an articular surface that is configured to increase a surface area of an articulation surface of a proximal portion of a posterior condyle of the femoral component. Other implementations are also discussed. | 10-02-2014 |
20150057756 | Patient Adapted Joint Arthroplasty Systems, Devices, Surgical Tools and Methods of Use - Improved systems, methods, and devices for performing joint arthroplasty, including patient-adapted implant components and tools, as well as intraoperative measurement and optimization of joint kinematics are disclosed herein. | 02-26-2015 |
20150081028 | ADAPTOR FOR MODULAR JOINT PROSTHESES - A bone augment adaptor is configured to be inseparably coupled to a bone augment. A first end of the adaptor is configured to be connected to an epiphyseal replacement portion of a modular joint replacement prosthesis. A second end of the adaptor may be configured to be connected to a diaphyseal anchoring portion of the prosthesis. | 03-19-2015 |
20160100950 | Total Knee Prostheses and Method for the Assembly Thereof - A method for assembling a total knee prosthesis is described, wherein portions of femoral and tibial implants, which are referred to as common portions and are each attachable in a femur and in a tibia of a knee, respectively, are assembled, and interchangeable portions are selected for adjustable assembly onto said common portions for each implant, respectively, depending on the type of prosthesis desired, some for a first posterior stabilization assembly configuration, and the others for a second rotary hinge assembly configuration. | 04-14-2016 |
20160128840 | Adjustable modular spacer device for the articulation of the knee - A knee spacer device configured to be implanted temporarily at the joint area between the tibia and femur of a patient to replace an infected joint prosthesis and to maintain the size or spaces of the patient's joint area before implanting a new prosthesis includes a tibial unit and a femoral unit. | 05-12-2016 |
20160166388 | COMPOSITE METALLIC-CERAMIC IMPLANTS AND RELATED METHODS | 06-16-2016 |
20160184107 | TIBIAL BEARING COMPONENT FOR A KNEE PROSTHESIS WITH IMPROVED ARTICULAR CHARACTERISTICS - 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. | 06-30-2016 |
20190142594 | IMPLANTS FOR ADDING JOINT INCLINATION TO A KNEE ARTHROPLASTY | 05-16-2019 |
623200160 | Bileaflet | 2 |
20100057201 | PROSTHETIC VALVE WITH VESSEL ENGAGING MEMBER - Medical devices for implantation in a body vessel are provided. Each medical device comprises a main body, a valve, and a vessel engaging member. The vessel engaging member is disposed on an outer surface of the main body. Kits including a plurality of vessel engaging members for use with one or more valve members are also provided. The vessel engaging members have varying radial dimensions, allowing assembly of medical devices having varying radial dimensions. Methods of treating a patient using medical devices according to the invention are also provided. | 03-04-2010 |
20120035720 | Method of Cutting Tissue Using a Laser - A prosthetic heart valve assembly comprises a plurality of leaflets configured to replace the function of a native heart valve. Each leaflet comprises laminar pericardium tissue. Each leaflet has a coaptation edge formed by laser cutting. The tissue layers of each leaflet are fused together along an entire length of the coaptation edge, and tissue adjacent each coaptation edge does not have significant thermal energy damage. | 02-09-2012 |
20080243257 | Method and apparatus for performing an open wedge, low femoral osteotomy - Apparatus for performing an open wedge, low femoral osteotomy, the apparatus comprising an osteotomy guide, a hinge pin and an osteotomy implant, the osteotomy guide comprising: anterior and posterior tissue shields having (i) openings for receiving the hinge pin and defining the hinge pin axis, and (ii) profiles configured to enable fluoroscopic alignment of the hinge pin axis parallel to the sagittal plane of the patient, a cutting guide comprising a cutting slot for defining a cutting plane extending parallel to, and through, the hinge pin axis, and a drill guide comprising a hole for forming a guide hole in the femur which extends substantially perpendicular to the cutting plane, the hinge pin comprising an elongated body, and the osteotomy implant for positioning in a wedge-shaped opening formed about the cutting plane and for receiving a screw extending through the guide hole. | 10-02-2008 |
20100076565 | Porous Titanium Femoral Sleeves and Their Use in Revision Knee Surgery - The invention concerns monolithic foam sleeves that comprises titanium or titanium alloy foam having a porosity of 50 to 85% and possess a proximal end, a distal end, an interior wall that defines an interior channel and extends from the proximal end to the distal end; and a terraced outer surface that tapers such that said sleeve is widest at the distal end and most narrow at the proximal end. | 03-25-2010 |
20100125337 | Trial implant and method of use - Disclosed is a trial implant having a body and a tab. The body may include a recess and may be sized to closely approximate a permanent implant. The tab may be more durable than the body, and may be disposed within the body and wholly contained within the recess. Also disclosed is a method of performing a trialing procedure including providing a trial implant as described, providing a tool to attach to the tab, inserting the implant onto a resected joint, evaluating and extracting the implant. The same procedure may then be performed with a second implant. The method may further include a tool having an attachment portion that is substantially or wholly contained within the recess. A kit is disclosed including a plurality of trial implants of incrementally different shapes and sizes. The kit may further include a tool. Also disclosed is a method of making the described implant. | 05-20-2010 |
20120185053 | Spacer Apparatus and Method for Achieving Improved Fit and Balance in Knee Joints - A spacer apparatus and method of using the same can be employed to achieve improved fit and balance in a knee joint in knee arthoplasty without requiring multiple cuts to the distal femur or proximal tibia. The spacer apparatus is composed of a biocompatible material in a lattice structure. The spacer apparatus can be pre-selected or pre-shaped, or can be selected or shaped at the time of use to have a thickness and shape appropriate to be used as a spacer to improve knee fit, or as a shim to improve knee balance. The spacer apparatus can be used in connection with a femoral implant, a tibial implant, or both. The spacer apparatus can be shaped to alter the orientation of a femoral or tibial implant in the varus/valgus orientation, the anterior/posterior orientation, or both. The spacer apparatus can be used singly or in combination with other spacer implants to improve fit and balance. | 07-19-2012 |
20130006370 | TRIALING SYSTEM FOR A KNEE PROSTHESIS AND METHOD OF USE - An orthopaedic surgical instrument system that includes an orthopaedic surgical instrument adapted to be positioned on a proximal end of a patient's tibia, and a tibial bearing trial assembly configured to be coupled to the orthopaedic surgical instrument. The tibial bearing trial assembly includes a plurality of tibial bearing surface trial components and at least one shim. | 01-03-2013 |
20130013076 | DYNAMIC KNEE BALANCER WITH PRESSURE SENSING - A device for performing a surgical procedure on a knee includes an adjustable femoral portion, a tibial. portion and at least one sensor coupled with the femoral and/or tibial portions to sense pressure exerted by the a moral and tibial portions against one another. The femoral portion is adapted for removably coupling with a distal end of a Femur to adjust tension in soft tissue adjacent the knee and has at least one positioning feature adapted to move relative to the distal end of the femur as the femoral portion is adjusted, thus helping position a femoral prosthetic on the distal end of the femur. The sensor(s) may he adapted to sense pressure at medial and lateral sides of the knee, and relative pressures may he displayed as data on a visual display. Adjustments to the femoral member may be made to balance pressure at flexion and extension of the knee. | 01-10-2013 |
20130338781 | Implants/Procedures Related to Tibial Tuberosity Advancement - A tibial tuberosity advancement (TTA) system is configured to maintaining a tuberosity in an advanced position relative to a tibial body. The TTA system includes an implant, a spacer, and a spacer fixation member. | 12-19-2013 |
20140114426 | KNEE JOINT DEVICE AND METHOD - A medical device for implantation in a knee joint of a human patient is provided. The medical device comprises: an inner surface ( | 04-24-2014 |
20140207243 | Implants for Altering Wear Patterns of Articular Surfaces - Methods and devices for correcting wear pattern defects in joints. The methods and devices described herein allow for the restoration of correcting abnormal biomechanical loading conditions in a joint brought on by wear pattern defects, and also can, in embodiments, permit correction of proper kinematic movement. | 07-24-2014 |
20140236306 | METHODS AND INSTRUMENTS FOR FORMING NON-CIRCULAR CARTILAGE GRAFTS - Techniques and instruments for knee replacement surgery that allow for the removal of an oval oblong-shaped allograft bone and cartilage plug from a donor distal femur. The instruments include (i) sizing guides to match the recipient's femoral size and curvature to that of a donor femur (the sizing guides also acting as a wide pin placement template for the donor distal femur); (ii) osteotomes that cut the curved and straight portions of the implant shape (these may be disposable or reusable); and (iii) templates that fit over the guide pins and have openings to allow the osteotomes to cut the donor femur plug to the correct size, shape and depth. The instruments allow for a non-circular shape to be extracted from a donor femur for use in a bone-saving osteoarthritis distal femur resurfacing procedure. | 08-21-2014 |
20140257500 | RESILIENT KNEE IMPLANT AND METHODS - This disclosure is directed to a resilient interpositional arthroplasty implant for application into a knee joint to pad cartilage defects, cushion a joint, and replace or restore the articular surface, which may preserve joint integrity, reduce pain and improve function. The implant may endure variable joint compressive and shear forces and cyclic loads. The implant may repair, reconstruct, and regenerate joint anatomy, and thereby improve upon joint replacement alternatives. Rather than using periosteal harvesting for cell containment in joint resurfacing, the walls of this invention may capture, distribute and hold living cells until aggregation and hyaline cartilage regrowth occurs. The implant may be deployed into debrided joint spaces, molding and conforming to surrounding structures with sufficient stability to avoid extrusion or dislocation. Appendages of the implant may repair or reconstruct tendons or ligaments, and an interior of the implant that is inflatable may accommodate motions which mimic or approximate normal joint motion. | 09-11-2014 |
20140277528 | KNEE AUGMENT - A knee prosthesis kit includes an implant and an augment. The implant has a base and a stem extending from the base, and the augment has a base and a conical, cylindrical, or anatomic portion extending from the base. The augment base has at least two openings for receiving fasteners for securing the knee augment to the implant. The portion and the base define a bore for receipt of the implant post. A coupler includes a mating portion for receipt in a bore of an implant post, and a cone-shaped portion extending from the mating portion. A method of providing fixation of knee implants includes securing an augment to an implant and positioning a conical, cylindrical, or anatomic portion of the augment within the intramedullary canal of the tibia or femur. | 09-18-2014 |
20140277529 | REMOVABLE AUGMENT FOR MEDICAL IMPLANT - An orthopaedic augment includes a porous material, which is removably attached to a medical implant. The porous material has a bone ingrowth surface for interfacing with an existing bone material and another surface for interfacing with the medical implant. | 09-18-2014 |
20140350685 | BONE-DERIVED IMPLANTABLE DEVICES FOR SUBCHONDRAL TREATMENT OF JOINT PAIN - Implantable devices for the surgical treatment of bone, and particularly to a bone defect at a joint region, and even more particularly at the subchondral bone level of the joint region, are disclosed. The implantable devices may be formed of a bone material, and configured to serve the dual functions of providing mechanical strength and structural integrity to the area to be treated, while also facilitating the dispersal of a flowable material in the same area. Associated delivery tools are also provided. | 11-27-2014 |
20160058560 | TIBIAL AUGMENTS FOR USE WITH KNEE JOINT PROSTHESES, METHOD OF IMPLANTING THE TIBIAL AUGMENT, AND ASSOCIATED TOOLS - A tibial augment for use with a knee joint prosthesis, composed of annular members of different stock sizes, each size being configured to fit within a cavity formed in a human tibia. The augment may include a stepped distal surface. A provisional (temporary) tibial augment used to ensure a proper fit for the permanent augment is also provided. The provisional may include grooves configured to cooperate with a set of ribs on a tong-like holder used for removing the provisional from the cavity. A pusher for use implanting the tibial augment is also provided. In addition, a system for creating a cavity in a human tibia is also described. The system preferably includes a guide with a slot therein and a set of osteotomes that are inserted within different portions of the slot. Methods for using the tools and/or implanting the prosthetic devices discussed above are also described. | 03-03-2016 |
20160151160 | Implants/Procedures Related to Tibial Tuberosity Advancement | 06-02-2016 |
20160193052 | PERIPROSTHETIC FRACTURE MANAGEMENT ENHANCEMENTS | 07-07-2016 |
20160250026 | METHOD FOR AMELIORATING JOINT CONDITIONS AND DISEASES AND PREVENTING BONE HYPERTROPHY | 09-01-2016 |
20170231774 | VOID FILLING JOINT PROSTHESIS AND ASSOCIATED INSTRUMENTS | 08-17-2017 |