A method is provided for facilitating the implantation of an implant during a surgical procedure. The method includes obtaining bone registration data for a first bone member and a second bone member of a patient's joint, and acquiring patient-specific movement-related data during the procedure after the joint is subjected to at least one movement with a first predefined distraction force applied throughout a continuous range of motions. A distraction force model is used to conduct a joint gap simulation based on predefined ligament stiffness data, the movement-related data at the first distraction force, and at least one simulation distraction force value, resulting in joint gap simulation data. A surgical plan model utilizes the joint gap simulation data and bone registration data to generate a patient-specific intra-operative surgical plan comprising at least one surgical cut parameter. The method further includes cutting the first and/or second bone member based on the surgical plan to facilitate implant implantation.
A61B 90/00 - Instruments, outillage ou accessoires spécialement adaptés à la chirurgie ou au diagnostic non couverts par l'un des groupes , p. ex. pour le traitement de la luxation ou pour la protection de bords de blessures
2.
METHODS FOR DIGITALLY ADJUSTING JOINT LAXITY IN A PERSONALIZED SURGICAL PLAN OF A JOINT ARTHROPLASTY PROCEDURE
A method for facilitating the implantation of an implant during a surgical procedure includes obtaining bone registration data for a first bone member and a second bone member of a patient's joint, and acquiring patient-specific movement-related data during the procedure after the joint is subjected to at least one movement with a first predefined distraction force applied throughout a continuous range of motions. A distraction force model is used to conduct a joint gap simulation based on predefined ligament stiffness data, the movement-related data at the first distraction force, and at least one simulation distraction force value, resulting in joint gap simulation data. A surgical plan model utilizes the joint gap simulation data and bone registration data to generate a patient-specific intra operative surgical plan comprising at least one surgical cut parameter. The method further includes cutting the first and/or second bone member based on the surgical plan.
A61B 34/10 - Planification, simulation ou modélisation assistées par ordinateur d’opérations chirurgicales
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p. ex. tremblement de la tête ou des mains ou mobilité d'un membre
G16H 50/50 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour la simulation ou la modélisation des troubles médicaux
A61F 2/46 - Outils particuliers pour l'implantation des articulations artificielles
A61B 34/00 - Chirurgie assistée par ordinateurManipulateurs ou robots spécialement adaptés à l’utilisation en chirurgie
A61B 34/20 - Systèmes de navigation chirurgicaleDispositifs pour le suivi ou le guidage d'instruments chirurgicaux, p. ex. pour la stéréotaxie sans cadre
05 - Produits pharmaceutiques, vétérinaires et hygièniques
10 - Appareils et instruments médicaux
Produits et services
Biological preparations for medical purposes. Bone void filler consisting of synthetic materials;
orthopedic joint implants made of artificial materials;
prosthetic and filling materials, namely, artificial
materials for use in the replacement of bones; surgical
implants comprising artificial materials for use with
orthopedic restoration and reconstruction procedures.
05 - Produits pharmaceutiques, vétérinaires et hygièniques
10 - Appareils et instruments médicaux
Produits et services
Biological preparations for medical purposes. Bone void filler consisting of synthetic materials;
orthopedic joint implants made of artificial materials;
surgical implants comprising artificial materials for use
with orthopedic restoration and reconstruction procedures;
prosthetic and filling materials, namely, artificial
materials for use in the replacement of bones.
05 - Produits pharmaceutiques, vétérinaires et hygièniques
10 - Appareils et instruments médicaux
Produits et services
(1) Biological preparations for medical purposes.
(2) Bone void filler consisting of synthetic materials; orthopedic joint implants made of artificial materials; surgical implants comprising artificial materials for use with orthopedic restoration and reconstruction procedures; prosthetic and filling materials, namely, artificial materials for use in the replacement of bones.
05 - Produits pharmaceutiques, vétérinaires et hygièniques
10 - Appareils et instruments médicaux
Produits et services
(1) Biological preparations for medical purposes.
(2) Bone void filler consisting of synthetic materials; orthopedic joint implants made of artificial materials; prosthetic and filling materials, namely, artificial materials for use in the replacement of bones; surgical implants comprising artificial materials for use with orthopedic restoration and reconstruction procedures.
A computer-implemented method including positioning at least one sensor within a joint of a patient; receiving, by a processor, a first data set representing a first series of reaction forces within the joint while the joint is moved through a range of motion; receiving, by the processor, a second data set representing a second series of reaction forces within the joint while the joint is moved through the range of motion while a first trial implant is attached within the joint; calculating, by the processor, a difference between the second data set and the first data set; and providing, by the processor, an instruction based on the difference, the instruction including either an instruction to select a second trial implant if the difference exceeds a threshold, or an instruction to proceed with an actual implant matching the first trial implant if the difference does not exceed the threshold.
Bone void filler consisting of synthetic materials; Orthopedic joint implants made of artificial materials; Surgical implants comprising artificial materials for use with orthopedic restoration and reconstruction procedures; Prosthetic and filling materials, namely, artificial materials for use in the replacement of bones
Bone void filler consisting of synthetic materials; Orthopedic joint implants made of artificial materials; Prosthetic and filling materials, namely, artificial materials for use in the replacement of bones; Surgical implants comprising artificial materials for use with orthopedic restoration and reconstruction procedures
A device including a housing having a passage extending therethrough defining a drive shaft axis; a drive shaft supported within the passage and rotatable about the drive shaft axis; a drive housing defining a reaming axis and pivotably coupled to the housing to allow the reaming axis to deflect with respect to the drive shaft axis, a drive interface supported within the drive housing and rotatable about the reaming axis, the drive interface contacting the drive shaft such that rotation of the drive shaft about the drive shaft axis causes rotation of the drive interface about the reaming axis; and an angle adjustment control positioned remotely from a distal end of the housing and operably coupled to the drive housing to move the drive housing between a first position and a second position to define respective first and second offset angles between the reaming axis and the drive shaft axis.
A surgery -facilitating system and method include a controller, a first tracker positioned on a first member of a joint, and a second tracker positioned on a second member of the joint. A first anatomical entity of the first member and a second anatomical entity of the second member are tracked using the first and second trackers to generate in the coordinate system, pre-operative kinematic data of the joint during a first movement of the joint, intra-operative kinematic data of the joint during a second movement of the joint, and post-operative kinematic data of the joint during a third movement of the joint. A surgical plan is generated for the surgical procedure of the subject based at least in part on the pre-operative kinematic data, the intra-operative kinematic data, or both, of the joint in the coordinate system.
A61B 34/10 - Planification, simulation ou modélisation assistées par ordinateur d’opérations chirurgicales
A61B 34/20 - Systèmes de navigation chirurgicaleDispositifs pour le suivi ou le guidage d'instruments chirurgicaux, p. ex. pour la stéréotaxie sans cadre
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p. ex. tremblement de la tête ou des mains ou mobilité d'un membre
A61F 2/46 - Outils particuliers pour l'implantation des articulations artificielles
A method includes receiving by a controller, a surgeon-specific surgery profile for an implantation of an implant into a joint, implant profiles, a patient-specific post-surgery desired functional profile of the joint after the implantation, and bone registration data for a first bone member and a second bone member of a patient are inputted into a surgical plan model to generate a surgical plan. The surgical plan model is designed to achieve the patient-specific post-surgery desired functional profile based at least in part on a plurality of dependencies between a plurality of surgical parameters, the implant profiles, at least one functional parameter representative of the expected functional performance of the joint, and movement-related data of the joint. The surgical plan is outputted on a graphical user interface (GUI) on a surgery assistant device to facilitate the implantation.
A device including a first plate configured to interface with a first bone structure of a joint; a second plate configured to interface with a second bone structure of the joint opposite the first bone structure; and at least one mechanical actuation mechanism disposed between the first plate and the second plate and configured to apply a distraction force along an axis between the first plate and the second plate so as to urge the first plate and the second plate away from one another, wherein the device is configured so as to have a range of motion ranging from a minimum distance between the first plate and the second plate to a maximum distance between the first plate and the second plate, and wherein the mechanical actuation mechanism is configured such that the distraction force is substantially constant distraction force across the range of motion.
A61B 5/103 - Dispositifs de mesure pour le contrôle de la forme, du dessin, de la dimension ou du mouvement du corps ou de parties de celui-ci, à des fins de diagnostic
An apparatus includes a processor and a non-transitory memory. The processor is configured to receive pre-operative patient specific data. The pre-operative patient specific data is inputted to a first machine learning model to determine a first predicted post-operative joint performance data output including first predicted post-operative outcome metrics. A reconstruction plan of the joint of the patient is generated based on a medical image of the joint, and at least one arthroplasty surgical parameter obtained from the user. The at least one arthroplasty surgical parameter is inputted into a second machine learning model to determine a second predicted post-operative joint performance data output including second predicted post-operative outcome metrics. The second predicted post-operative joint performance data output is updated to include an arthroplasty surgery recommendation, in response to the user varying the at least one arthroplasty surgical parameter, before the arthroplasty surgery, during the arthroplasty surgery, or both.
A61F 2/00 - Filtres implantables dans les vaisseaux sanguinsProthèses, c.-à-d. éléments de substitution ou de remplacement pour des parties du corpsAppareils pour les assujettir au corpsDispositifs maintenant le passage ou évitant l'affaissement de structures corporelles tubulaires, p. ex. stents
A selection system comprises a ring, a plurality of shims, a measurement device, and at least one glenoid component. The ring is configured to couple to a humerus. A shim of the plurality of shims is configured to couple to the ring. The measurement device is configured to couple to the shim. Each shim of the plurality of shims has a different height when coupled to the ring. The selection system generates measurement data to support the selection of at least one prosthetic component for a shoulder joint in a surgical environment. The shoulder joint geometry can be adjusted by changing shims, changing glenoid component or both. The selection system is removed after the selection of the final prosthetic components for the shoulder joint. The final prosthetic components are installed in the shoulder joint. The measurement device is placed in the shoulder joint and measurement data is generated to verify performance.
09 - Appareils et instruments scientifiques et électriques
10 - Appareils et instruments médicaux
Produits et services
Downloadable computer software for use in orthopedic joint
surgery; computer hardware and software for use in
orthopedic joint surgery; downloadable medical software for
use in balancing and tensioning ligaments and joints in
surgery. Medical apparatus and instruments for use in orthopedic
surgery; electronic medical device for use in balancing and
tensioning ligaments and joints in surgery.
09 - Appareils et instruments scientifiques et électriques
10 - Appareils et instruments médicaux
Produits et services
downloadable computer software for use in orthopedic joint surgery; computer hardware and downloadable software for use in orthopedic joint surgery; downloadable medical software for use in balancing and tensioning ligaments and joints in surgery medical apparatus and instruments for use in orthopedic surgery; Electronic medical device for use in balancing and tensioning ligaments and joints in surgery
28.
Measurement system for a selection of at least one prosthetic component of a shoulder joint during surgery
A selection system comprises a ring, a plurality of shims, a measurement device, and at least one glenoid component. The ring is configured to couple to a humerus. A shim of the plurality of shims is configured to couple to the ring. The measurement device is configured to couple to the shim. Each shim of the plurality of shims has a different height when coupled to the ring. The selection system generates measurement data to support the selection of at least one prosthetic component for a shoulder joint in a surgical environment. The shoulder joint geometry can be adjusted by changing shims, changing glenoid component or both. The selection system is removed after the selection of the final prosthetic components for the shoulder joint. The final prosthetic components are installed in the shoulder joint. The measurement device is placed in the shoulder joint and measurement data is generated to verify performance.
A kit including (1) a plate configured to be secured to a scapular spine with a first end of the plate near a trigonum and a second end of the plate near an acromion; (2) a first hook including a mount, a first hook portion extending from the mount in a first direction, a spacer extending from the first hook portion in a transverse direction, and a second hook portion extending from an opposite end of the spacer in the first direction, the first hook adapted to extend around a lateral end of the acromion when fixed to the second end of the plate; and (3) a second hook including a mount, a curved portion curving away from the mount, and a hook portion at an opposite end of the curved portion, the second hook adapted to extend around the trigonum when fixed to the first end of the plate.
A61B 17/70 - Dispositifs de mise en position ou de stabilisation de la colonne vertébrale, p. ex. stabilisateurs comprenant un liquide de remplissage dans un implant
A device includes an acromion portion sized and shaped to replicate functions of the native acromion, and a fixation portion connected to the acromion portion, the fixation portion including a first arm portion and a second arm portion spaced apart from the first arm portion, wherein the first arm and second arm portions are positioned such that, when the device is positioned such that the acromion portion is in a native position of the absent native acromion, the first arm portion overlays a superior face of a scapular spine of the scapula and the second arm portion overlays an inferior space of the scapular spine of the scapula, wherein each of the first arm portion and the second arm portion includes at least one screw fixation point extending therethrough and configured to receive a screw therein so as to secure the device to the scapula.
42 - Services scientifiques, technologiques et industriels, recherche et conception
Produits et services
providing temporary use of on-line non-downloadable software for assisting orthopedic surgeons with determining the best course of treatment for particular patients and improve post-operative results
A computer-implemented method including positioning at least one sensor within a joint of a patient; receiving, by a processor, a first data set representing a first series of reaction forces within the joint while the joint is moved through a range of motion; receiving, by the processor, a second data set representing a second series of reaction forces within the joint while the joint is moved through the range of motion while a first trial implant is attached within the joint; calculating, by the processor, a difference between the second data set and the first data set; and providing, by the processor, an instruction based on the difference, the instruction including either an instruction to select a second trial implant if the difference exceeds a threshold, or an instruction to proceed with an actual implant matching the first trial implant if the difference does not exceed the threshold.
A61F 2/00 - Filtres implantables dans les vaisseaux sanguinsProthèses, c.-à-d. éléments de substitution ou de remplacement pour des parties du corpsAppareils pour les assujettir au corpsDispositifs maintenant le passage ou évitant l'affaissement de structures corporelles tubulaires, p. ex. stents
Coating sold as an integral component of implantable orthopedic devices; surgical implants comprising artificial materials for use with orthopedic restoration and reconstruction procedures
A proximal portion of an implant for repairing a multipart fracture of a proximal humerus includes an asymmetric body having a proximal end, a distal end, a medial side, a lateral side, an anterior edge, and a posterior edge a medial surface extending along at least a portion of the medial side and having a proximal end and a distal end; a protrusion forming the lateral side of the asymmetric body, offset in an anterior direction, and pointing toward a bicipital groove of the humerus when the proximal portion is implanted in the humerus, an anterior support surface configured to support a lesser tuberosity; a posterior support surface configured to support a greater tuberosity; an angled surface having a first side defined by the medial surface, a second side defined by the anterior support surface, and a third side defined by the posterior support surface; and an anchoring point.
Surgical implants, namely, implantable orthopedic hip prosthesis, as well as kits and systems containing an implantable hip prosthesis and an assortment of fixation hardware, namely, screws, cables and hooks, and written instructions sold as a kit
A drug-eluting spacer for temporary implantation in a knee joint includes a femoral component configured to interface with a femur, a tibial tray component having an upper surface, a lower surface, and a shaft extending from the lower surface, the shaft configured to be positioned axially within a tibia, the lower surface configured configured to interface with the tibia, and a tibial insert component having an upper surface and a lower surface, the lower surface of the tibial insert component configured to engage the upper surface of the tibial tray component, the upper surface of the tibial insert component configured to receive the femoral component in an articulating manner. The femoral component, the tibial tray component, and the tibial insert component carry joint loads when implanted. The drug-eluting spacer is configured to elute a biologically active agent in an amount effective to treat an infection of the knee joint.
A kit includes a distractor, a plurality of trial elements, and at least one sensor. The distractor is configured to separate a first bone from a second bone by adjusting the distance between a first member and a second member, and is configured to receive at least one sensor in the first portion. Each of the trial elements corresponds to one of a plurality of surgical implants, is configured to be temporarily coupled to the second bone so as to evaluate suitability of the corresponding one of the plurality of surgical implants for implantation, and is configured to receive at least one sensor. The at least one sensor is configured to be received in the distractor or one of the trial elements, and is configured to record a magnitude of a force, a direction of application of a force, a pressure mapping, or a location of application of a force.
A61B 17/56 - Instruments ou procédés chirurgicaux pour le traitement des os ou des articulationsDispositifs spécialement adaptés à cet effet
A61B 17/58 - Instruments ou procédés chirurgicaux pour le traitement des os ou des articulationsDispositifs spécialement adaptés à cet effet pour ostéosynthèse, p. ex. plaques, vis ou matériels de fixation
A61B 17/60 - Instruments ou procédés chirurgicaux pour le traitement des os ou des articulationsDispositifs spécialement adaptés à cet effet pour ostéosynthèse, p. ex. plaques, vis ou matériels de fixation pour l'ostéosynthèse externe, p. ex. appareils étireurs ou constricteurs
A61B 5/03 - Mesure de la pression des fluides à l'intérieur du corps autre que la pression du sang, p. ex. de la pression cérébrale
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p. ex. tremblement de la tête ou des mains ou mobilité d'un membre
A61F 2/38 - Articulations pour les coudes ou les genoux
In some embodiments, the present invention provides a reverse shoulder glenoid prosthesis which supports the attachment of multiple different types of modular attachments that can: 1) provide additional scapular fixation (ie external to the glenoid) in order to improve glenoid implant fixation in cases of severe bone loss/fracture, 2) provide joint line lateralization to improve tissue stability in cases of severe glenoid/scapula bone loss, 3) facilitate use and containment of glenoid bone graft in cases of severe glenoid/scapula bone loss - particularly in those cases in which the glenoid defect is uncontained/peripheral 4) achieve glenoid fixation while at the same time reconstructing the scapular bone in cases of scapula fractures, glenoid fractures, and/or acromial fractures, and 5) provide improved rTSA joint biomechanics, particularly posterior rotator cuff efficiency by changing the line of action of the infraspinatus and teres minor muscles to improve their muscle tension, and also increase each muscle's external rotation and abduction moment arm lengths.
A61F 2/00 - Filtres implantables dans les vaisseaux sanguinsProthèses, c.-à-d. éléments de substitution ou de remplacement pour des parties du corpsAppareils pour les assujettir au corpsDispositifs maintenant le passage ou évitant l'affaissement de structures corporelles tubulaires, p. ex. stents
Adaptable medical trays are disclosed herein. An adaptable medical tray includes a first component medical tray having a plurality of walls, a bottom, and a removable top, the plurality of walls and the bottom arranged to form a cavity in the first component medical tray; and a second component medical tray removably coupled to the first component medical tray, the second component medical tray including a plurality of walls, a bottom, and a removable top, the plurality of walls and the bottom arranged to form a cavity in the second component medical tray. The first component medical tray and the second component medical tray are constructed of a sterilizable material and the first component medical tray is decouplable from the second component medical tray after a sterilization process without removing the removable tops from the cavities.
A61B 50/30 - Récipients spécialement adaptés à l'emballage, la protection, la distribution, la collecte ou l'élimination des appareils ou des instruments chirurgicaux ou de diagnostic
A61B 50/00 - Récipients, étuis, mobilier ou supports spécialement adaptés aux appareils ou aux instruments chirurgicaux ou de diagnostic, p. ex. étuis stériles
A talar implant, comprising: a superior surface, defined by an arc having at least one first radius; an inferior surface, defined by an arc having at least one second radius, a lateral side; a medial side; a posterior portion having a first width; and an anterior portion having a second width; wherein the implant is configured to restore a tibio-talar joint tension, wherein the superior surface is separated from the inferior surface by a thickness, wherein the at least one first radius is smaller than the at least one second radius, wherein the center of the arc having at least one first radius is offset from the center of the arc having at least one second radius in at least one plane of the talar implant, and wherein the anterior portion further comprises an extension configured to provide support.
A61F 2/42 - Articulations pour les poignets ou les chevillesArticulations pour les mains, p. ex. pour les doigtsArticulations pour les pieds, p. ex. pour les orteils
In one embodiment, the present invention provides an augment comprising: a. a side configured to contact and attach to a receiving bone; b. a side configured to contact an implant; and c. an exterior profile, wherein the side configured to contact a receiving bone and the side configured to contact an implant are separated by a thickness; and wherein the augment is configured to anchor to the receiving bone.
Disclosed is a prosthetic augment designed to reconstruct a lateral tuberosity shape of a humerus in a subject having proximal bone loss that includes a humeral adapter tray configured to connect a humeral liner of a reverse shoulder prosthesis to a humeral stem of the reverse shoulder prosthesis and an augment member having a first face adapted for contacting the humeral stem of the reverse shoulder prosthesis and a second face adapted for contacting an underside of a muscle, wherein at least a portion of the second face includes a bulbous surface adapted to alter a wrapping angle of the muscle around the lateral tuberosity, and wherein the second face has a radius of curvature selected from one of a constant radius of curvature or a variable radius of curvature.
In some embodiments, an intervertebral implant may include a body including a superior and an inferior surface. The implant may include a first channel extending from an anterior end towards the posterior end of the body. The implant may include a first anchor channel. The implant may include a first guide member positionable in the first channel. The implant may include a first anchor. When the first guide member moves from a first position to a second position the first anchor may be conveyed through the first anchor channel and couple the body to an adjacent vertebra.
A61F 2/44 - Articulations pour l'épine dorsale, p. ex. vertèbres, disques intervertébraux
A61B 17/70 - Dispositifs de mise en position ou de stabilisation de la colonne vertébrale, p. ex. stabilisateurs comprenant un liquide de remplissage dans un implant
A prosthesis system (100) of the present invention includes a monoblock stem extension (10) comprising a proximal portion (20) having a first neutral axis (20a); and a distal portion (30) defined by a longitudinal cylindrical shaft (31) having a. second neutral axis (30a), wherein the second neutral axis (30a) is parallel and offset by a distance a from the first neutral axis (20a): and an eccentric bushing (50) arranged coaxial around the cylindrical shaft (31) of the monoblock stem extension ( 10), the eccentric bushing (50) comprising an external cylindrical shaft (51 ) having a third neutral axis (51a); and an internal cylinder (53) having a fourth neutral axis (50a) that is substantially co-linear with the second neutral axis (30a) of the monoblock stem extension (10), wherein the third neutral axis (5 l a) is parallel and offset by a distance β from the fourth neutral axis (50a).
Surgical implants, namely, implantable orthopedic hip
prostheses; medical instruments and tools for use with hip
replacement and repair and written instructions for hip
replacement and repair surgery sold as a unit therewith.
Surgical implants, namely, implantable orthopedic ankle prostheses; medical instruments and tools for use with ankle replacement and repair and written instructions for ankle replacement and repair surgery sold as a unit therewith
Surgical implants, namely, artificial implantable orthopedic hip prostheses; medical instruments and tools for use with hip replacement and repair and written instructions for hip replacement and repair surgery sold as a unit therewith
Surgical implants comprising of artificial materials, namely, implantable orthopedic knee prostheses; surgical implant kits containing implantable knee prosthesis components and fixation hardware such as screws, cables, hooks, and written instructions, sold as a unit
63.
PROSTHETIC DEVICES TO IMPROVE JOINT MECHANICS IN ARTHROPLASTY
Disclosed herein is a kit that includes a humeral stem having a central longitudinal axis, the humeral stem configured to attach to a resected bone; a first tuberosity component having a first thickness relative to the central longitudinal axis of the humeral stem; a second tuberosity component having a second thickness relative to the central longitudinal axis of the humeral stem, wherein the first thickness of the first tuberosity component is different than the second thickness of the second tuberosity component; and at least one proximal segment configured to engage at least one of the first tuberosity component and the second tuberosity component. In an embodiment, the first thickness of the first tuberosity component is at least 20mm relative to the central axis of the humeral stem, and the second thickness of the second tuberosity component is at least 20 mm relative to the central axis of the humeral stem.
A reverse shoulder prosthesis includes a humeral adapter tray (300) configured to sit near a resected surface of a humerus, the humeral adapter tray (300) comprising: a cavity (302); a central bore; and a distal face (304) including a boss (310), the boss (310): (i) configured as an extension of the distal face, (ii) posteriorly offset from the central bore by at least 10 mm, and (iii) configured to engage a humeral stem; and a humeral liner (250) comprising: a distal rim (252) configured to sit within the cavity (302) of the humeral adapter tray (300); and a concave articulating surface configured to mate with a convex articulating surface of a glenosphere. Offsetting the reverse shoulder humeral adapter tray shifts the humerus in the posterior direction so as to result in better deltoid wrapping, more anatomic muscle tensioning, and larger muscle moment arms during both abduction and internal/external rotation.
A61B 17/58 - Instruments ou procédés chirurgicaux pour le traitement des os ou des articulationsDispositifs spécialement adaptés à cet effet pour ostéosynthèse, p. ex. plaques, vis ou matériels de fixation
A glenoid assembly includes a glenoid plate (110) configured for fixation to a glenoid bone; a glenosphere (108) configured for connection to the glenoid plate (110); and an adjustment plate (140), wherein the adjustment plate (140) has a connection for directly engaging the glenosphere (108), and wherein the adjustment plate (140) has an articulation for directly engaging the glenoid plate (110) at a variable angular orientation. A method includes, fixating a glenoid plate (110) to a glenoid bone; locking an adjustment plate (140), configured for interfacing with both the glenoid plate (110) and a glenosphere (108), to the glenoid plate (110), wherein the adjustment plate (140) is configured for angular orientation or positional change relative to the glenoid plate (110); connecting a glenosphere (108) to the adjustment plate (140); and independently adjusting an angular orientation and position of the glenosphere (108) relative to the fixated glenoid plate (110).
In an embodiment, the methodology of the present invention is based on the use of an intraoperative navigation system and of a compact alignment guide for alignment of implant components. In an embodiment, an alignment guide of the present invention includes a first component fixable to a bone element; a second mobile component, and a third mobile component, wherein the second mobile component and two control mechanisms form a first link, wherein the two control mechanisms are working in parallel to perform adjustments in two degrees of freedom, wherein the third mobile component and three control mechanisms form a second link, wherein the three control mechanisms are working in parallel to perform adjustments in three additional degrees of freedom, and wherein the first link adjustments and the second link adjustments are performed in series to provide a total adjustment of five degrees of freedom relative to the first component.
A61B 17/58 - Instruments ou procédés chirurgicaux pour le traitement des os ou des articulationsDispositifs spécialement adaptés à cet effet pour ostéosynthèse, p. ex. plaques, vis ou matériels de fixation
67.
FLEXIBLE INTERVERTEBRAL SPACERS AND ASSOCIATED METHODS
Flexible intervertebral spacers and associated methods are disclosed herein. In one embodiment, an intervertebral spacer includes a first support member configured to engage a superior vertebra of a spine, a second support member configured to engage an inferior vertebra of the spine, and a joint coupling the first support member to the second support member. The joint is adapted to limit the transverse relationship between the first and second support members while allowing relative movement between the first and second support members relative to each other during flexion, extension, bending, and rotation of the spine.
A61F 2/44 - Articulations pour l'épine dorsale, p. ex. vertèbres, disques intervertébraux
A61B 17/70 - Dispositifs de mise en position ou de stabilisation de la colonne vertébrale, p. ex. stabilisateurs comprenant un liquide de remplissage dans un implant
A61B 17/82 - Dispositifs de fixation interne pour le cerclage des os
Methods, systems, devices and tools for placing bone stabilization components in a patient are provided. The systems and devices have a reduced number of discrete components that allow placement through small incisions and tubes. More particularly, the present invention is directed to systems and methods of treating the spine, which eliminate pain and enable spinal motion. Methods are also provided for stabilizing the thoracolumbar spine region and for implanting the disclosed systems.
A61B 17/70 - Dispositifs de mise en position ou de stabilisation de la colonne vertébrale, p. ex. stabilisateurs comprenant un liquide de remplissage dans un implant
A61B 17/88 - Moyens ou procédés pour implanter ou pour extraire des dispositifs de fixation interne
A61F 2/44 - Articulations pour l'épine dorsale, p. ex. vertèbres, disques intervertébraux
One embodiment of the present invention relates to a reverse shoulder assembly. Another embodiment of the present invention relates to a reverse shoulder assembly method of use. In one example, a reverse shoulder assembly of the present invention may be provided such that the reverse shoulder assembly alters the abduction force created by a patient's deltoid to a forward flexion force. In one example, a reverse shoulder assembly of the present invention may be provided such that the reverse shoulder assembly alters the abduction force created by a patient's deltoid to an external rotation force. In one example, a reverse shoulder assembly of the present invention may be provided such that the reverse shoulder assembly alters the abduction force created by a patient's deltoid to an external rotation force and a forward flexion force.
Surgical implants comprising artificial material, namely,
implantable orthopedic knee prosthesis and kits containing
an implantable knee prosthesis and an assortment of fixation
hardware, including screws, cables, hooks, and written
instructions all packaged as a unit.
Medical apparatus and instruments for use in orthopedic
surgery.
74.
SYSTEMS AND METHODS RELATING TO A KNEE PROSTHESIS CAPABLE OF CONVERSION FROM A CRUCIATE RETAINING TYPE PROSTHESIS TO A POSTERIOR STABLIZING TYPE PROSTHESIS
One embodiment of the present invention relates to a system in which a knee prosthesis is capable of conversion from a cruciate retaining type prosthesis to a posterior stabilizing type prosthesis Another embodiment of the present invention relates to a system in which a knee prosthesis is converted from a cruciate retaining type prosthesis to a posterior stabilizing type prosthesis Another embodiment of the present invention relates to a method in which a knee prosthesis is capable of conversion from a cruciate retaining type prosthesis to a posterior stabilizing type prosthesis Another embodiment of the present invention relates to a method in which a knee prosthesis is converted from a cruciate retaining type prosthesis to a posterior stabilizing type prosthesis.
A dynamic rod implantable into a patient and connectable between two vertebral anchors in adjacent vertebral bodies is provided. The dynamic rod fixes the adjacent vertebral bodies together in a dynamic fashion providing immediate postoperative stability and support of the spine. The dynamic rod comprises a first rod portion dynamically connected to a second rod portion at a retainer that has separate chambers for receiving rod portions. One rod portion is configured for longitudinal movement and the other rod portion is configured for polyaxial angulation relative to the retainer. The dynamic rod is configured such that the retainer is located proximate to one of the facet joints when implanted into a patient. The dynamic rod permits relative movement of the first and second rod portions allowing the rod to carry some of the natural flexion, extension and rotation moments of the spine.
A61B 17/70 - Dispositifs de mise en position ou de stabilisation de la colonne vertébrale, p. ex. stabilisateurs comprenant un liquide de remplissage dans un implant
Surgical implants comprising artificial and or biological
materials for use with orthopedic, spinal, and dental bone
restoration and reconstruction procedures; prosthetic and
filling materials, namely, artificial materials for use in
the replacement of bones; surgical instruments for use in
the field of orthopedic and spinal surgery.
One embodiment of the present invention relates to a knee prosthesis system with at least a first tibial portion element (a tibial insert or a tibial insert trial) and a second tibial portion element (a tibial insert or a tibial insert trial), wherein each of the first tibial portion element and the second tibial portion element has a different slope. Another embodiment of the present invention relates to a method of implanting a knee prosthesis, wherein the method utilizes at least a first tibial portion element (a tibial insert or a tibial insert trial) and a second tibial portion element (a tibial insert or a tibial insert trial), wherein each of the first tibial portion element and the second tibial portion element has a different slope.
05 - Produits pharmaceutiques, vétérinaires et hygièniques
10 - Appareils et instruments médicaux
Produits et services
Surgical implants comprising biological materials for use with orthopedic, spinal, and dental bone restoration and reconstruction procedures Surgical implants comprising artificial materials for use with orthopedic, spinal, and dental bone restoration and reconstruction procedures; prosthetic and filling materials, namely, artificial materials for use in the replacement of bones; surgical instruments for use in the field of orthopedic and spinal surgery
05 - Produits pharmaceutiques, vétérinaires et hygièniques
Produits et services
Bone cement for medical purposes; human allograft bone and tissue; biological preparations for medical purposes
84.
FEMORAL COMPONMENT OF KNEE PROSTHESIS, THE FEMORAL COMPONENT HAVING ANTERIOR/POSTERIOS CLAW(S) FOR DIGGING INTO BONE AND/OR A RAISED RIB WITH A BULBOUS TERMINUS
One embodiment of the present invention provides a femoral component of a knee prosthesis, wherein the femoral component include a sharp radius at each end (e g, the anterior end and the posterior end) of the femoral component. The sharp radius at each end may form a 'claw' at each end.Each of these claws may 'dig' through the patient's cartilage into the bone (or may 'dig' directly into bone if there is no intervening cartilage). Enhanced fixation may be achieved with the claws 'digging' and fixing into the bone as well as the claws providing additional cement pressurization (e g, with the claws in the bone, cement is less likely to escape by the anterior and posterior ends). Further, one benefit provided by a claw may be facilitating a smooth transition of cartilage/poly bearing to femoral implant/poly bearing (e g, during knee extension).
05 - Produits pharmaceutiques, vétérinaires et hygièniques
10 - Appareils et instruments médicaux
Produits et services
Surgical implants comprising biological materials for use with orthopedic, spinal, and dental bone restoration and reconstruction procedures Surgical implants comprising artificial materials for use with orthopedic, spinal, and dental bone restoration and reconstruction procedures; prosthetic and filling materials, namely, artificial materials for use in the replacement of bones; surgical instruments for use in the field of orthopedic and spinal surgery
One embodiment of the present invention relates to a prosthesis, comprising an acetabular cup, wherein the cup has an open end and a closed end, wherein the open end of the cup is defined by a nm and wherein the rim has an outer facing surface, at least one cavity disposed in the rim, wherein the cavity extends from a first end of the cavity at the outer facing surface to a second end of the cavity that is towards the closed end of the cup, and wherein the cavity comprises an undercut at the second end of the cavity, a locking ring, and at least one tab extending from the locking ring, wherein the tab comprises a first leg and a second leg having a separation therebetween, wherein each leg has a first end and a second end.
Surgical implants, namely, implantable orthopedic hip
prosthesis, as well as kits and systems containing an
implantable hip prosthesis and an assortment of fixation
hardware, including screws, cables and hooks for use in
orthopedic surgery.
90.
SYSTEM AND METHOD FOR ADJUSTING THE THICKNESS OF A PROSTHESIS
The present invention relates to a system and method for adjusting a thickness of a prosthesis. A knee prosthesis for implantation may be provided, comprising: a tibial tray, wherein the tibial tray comprises an upper surface and a lower surface, and the lower surface of the tibial tray is disposed adjacent a tibia of the patient; a tibial insert, with an upper surface and a lower surface; a tibial spacer, with an upper surface and a lower surface. The spacer is disposed between the tibial tray and the tibial insert such that the lower surface of the tibial spacer is adjacent the upper surface of the tibial tray and the upper surface of the tibial spacer is adjacent the lower surface of the tibial insert; and at least one locking mechanism, wherein the locking mechanism locks the tibial spacer to the tibiat tray to form a locked spacer/tray assembly.
Surgical implants comprising artificial material, namely,
implantable orthopedic hip prosthesis; kits comprised
primarily of an implantable hip prosthesis and an assortment
of fixation hardware, including screws, cables and hooks for
use in hip joint replacement surgery.
SURGICAL IMPLANTS, NAMELY, IMPLANTABLE ORTHOPEDIC HIP PROSTHESIS, AS WELL AS KITS AND SYSTEMS CONTAINING AN IMPLANTABLE HIP PROSTHESIS AND AN ASSORTMENT OF FIXATION HARDWARE, INCLUDING SCREWS, CABLES AND HOOKS, AND WRITTEN INSTRUCTIONS
Surgical implants comprising artificial material, namely, implantable orthopedic knee prosthesis and kits containing an implantable knee prosthesis and an assortment of fixation hardware, including screws, cables, hooks, and written instructions all packaged as a unit
Surgical implants, namely, implantable orthopedic hip prostheses; kits and systems for use in implanting hip prosthetics comprising an implantable hip prosthesis, fixation hardware such as screws, cables and hooks, and written instructions for hip replacement and repair surgery, sold as a unit; medical instruments and tools for use with hip replacement and repair and written instructions for hip replacement and repair surgery sold as a unit therewith
Surgical apparatus for use in the field of orthopedic surgery, namely, pneumatically powered hand drivers and parts and accessories used therewith, namely, osteotomes, gouges, punches and impactors
Surgical implants comprising artificial material, namely, implantable orthopedic hip prosthesis; kits comprised primarily of an implantable hip prosthesis and an assortment of fixation hardware, including screws, cables and hooks for use in hip joint replacement surgery
Medical devices namely, orthopedic implants composed of processed ortho-biologic materials and related instrumentation, and fixation hardware, namely screws, cables and hooks, and written instructions included therewith
Surgical implants comprising artificial material, namely, implantable orthopedic knee prosthesis and kits containing an implantable knee prosthesis and an assortment of fixation hardware, including screws, cables, hooks, and written instructions all packaged as a unit
