Abstract: A method of replacing a native cardiac valve with a prosthetic cardiac valve, the method comprising: expanding a wire mesh scaffolding in a chamber of the heart on a retrograde side of the native cardiac valve; while the scaffolding is expanded on the retrograde side of the valve positioning the prosthetic cardiac valve at the site of the native cardiac valve; expanding the prosthetic cardiac valve to replace the native cardiac valve; and collapsing the scaffolding to a collapsed state and removing the collapsed scaffolding from the chamber of the heart.

Abstract: Prosthetic heart valve devices for percutaneous replacement of native heart valves and associated systems and method are disclosed herein. A prosthetic heart valve device configured in accordance with a particular embodiment of the present technology can include an expandable support having an outer surface and configured for placement between leaflets of the native valve. The device can also include a plurality of asymmetrically arranged arms coupled to the expandable support and configured to receive the leaflets of the native valve between the arms and the outer surface. In some embodiments, the arms can include tip portions for engaging a subannular surface of the native valve.

Abstract: Apparatus for use with a prosthetic heart valve includes a holder, to which the heart valve is releasably attached, and an elongated handle. The handle can be connected to the holder simply by pushing a distal end of the handle straight into a recess in the holder. After this has been done, the holder preferably releasable latches onto the handle, and the handle can also be rotated about its longitudinal axis to transmit torque to the holder (e.g., a rotatable portion of the holder). Rotation of such a rotatable portion of the holder can be used to deflect portions of the valve radially inward. This operation of a rotatable portion of the holder is preferably one-way only. The handle can be released from the holder at any time, and it can similarly be reconnected to the holder at any time.

Abstract: A prosthetic heart valve is provided with a cuff having features which promote sealing with the native tissues even where the native tissues are irregular. The cuff may include a portion adapted to bear on the LVOT when the valve is implanted in a native aortic valve. The valve may include elements for biasing the cuff outwardly with respect to the stent body when the stent body is in an expanded condition. The cuff may have portions of different thickness distributed around the circumference of the valve in a pattern matching the shape of the opening defined by the native tissue. All or part of the cuff may be movable relative to the stent during implantation.

Abstract: A device for providing cardiac treatment at the left atrium of a patient's heart. The device includes a retention body and a prosthetic valve. The retention body has a shape that can be manipulated between a collapsed state and a normal or expanded state. First and second openings are defined at one side of the retention body, and a lower opening is defined at an opposite side. The prosthetic valve is carried by the retention body at the lower opening. The retention body is configured to engage a substantial portion of an interior surface of the left atrium, securing the prosthetic valve at a desired location relative to a native mitral valve (e.g., within the mitral valve or slightly spaced from the mitral valve). The first and second openings are sized and shaped so as to permit blood flow from the pulmonary veins into the interior region.

Abstract: Prosthetic heart valve devices for percutaneous replacement of native heart valves and associated systems and method are disclosed herein. A prosthetic heart valve device configured in accordance with a particular embodiment of the present technology can include an expandable support having an outer surface and configured for placement between leaflets of the native valve. The device can also include a plurality of asymmetrically arranged arms coupled to the expandable support and configured to receive the leaflets of the native valve between the arms and the outer surface. In some embodiments, the arms can include tip portions for engaging a subannular surface of the native valve.

Abstract: A delivery device for a collapsible prosthetic heart valve includes a support shaft around which a compartment is defined, an inner shaft extending through the support shaft and adapted to slide relative to the support shaft along a longitudinal axis thereof, the inner shaft having a lumen therethrough, and a distal sheath operatively connected at a distal end to the inner shaft and slidable therewith. The compartment may receive the valve in an assembled condition, and may be selectively covered and uncovered by the distal sheath. A first flow path may provide flow communication between the lumen of the inner shaft and the compartment.

Abstract: Devices and methods are disclosed for the treatment or repair of regurgitant cardiac valves, such as a mitral valve. An annuloplasty device can be placed in the coronary sinus to reshape the mitral valve and reduce mitral valve regurgitation. A protective device can be placed between the annuloplasty device and an underlying coronary artery to inhibit compression of the underlying coronary artery by the annuloplasty device in the coronary sinus. In addition, the protective device can inhibit compression of the coronary artery from inside the heart, such as from a prosthetic mitral valve that exerts radially outward pressure toward the coronary artery. The annuloplasty device can also create an artificial inner ridge or retaining feature projecting into the native mitral valve region to help secure a prosthetic mitral valve.

Abstract: Disclosed are methods, systems, and devices for the endovascular repair of cardiac valves, particularly the atrioventricular valves which inhibit back flow of blood from a heart ventricle during contraction. The procedures described herein can be performed with interventional tools, guides and supporting catheters and other equipment introduced to the heart chambers from the patient's arterial or venous vasculature remote from the heart. The interventional tools and other equipment may be introduced percutaneously or may be introduced via a surgical cut down, and then advanced from the remote access site through the vasculature until they reach the heart.

Abstract: Disclosed herein are implants and methods for filling voids in a cranium of a patient. A craniofacial implant that may be used for filling such voids may include at least first and second components each having outer and inner surfaces, the outer and inner surfaces being curved in an inferior to posterior direction and a medial to lateral direction. The first component includes a flange extending outwardly from a medial side surface thereof and the second component includes a recessed portion extending inwardly from a medial side surface thereof. The first and second components are preferably engageable to one another such that the medial side surfaces of the first and second components are adjacent one another and the flange of the first component is housed within the recessed portion of the second component.

Abstract: A skeletal replacement system may be utilized to replace bones in a patient. The skeletal replacement system has least one skeletal replacement linkage, each skeletal replacement linkage having a first member, a second member, and a hinge. The first and second members are hingedly coupled by the hinge. Multiple skeletal replacement linkages may be coupled end to end through a shaft on the second member of a first linkage being inserted into a bore in the first member of a second linkage. Each linkage is configured to replace at least a portion of each of two bones and a joint in a patient's body. Multiple linkages may be used to replace more bones and joints as required.

Abstract: The present invention relates to orthopaedic implants having a fenestrated hollow shell and a biologic core. These design features provide an improved interface between the implant and the surrounding tissue aiding fixation, and provide a vehicle for applying new bone healing and enhancing modalities, such as gene therapy, tissue engineering, and growth factors.

Abstract: Implants and procedures far joint fusion make use of implants comprising cortical bone. The implants have lamellae that are generally aligned. In some embodiments, the implants can have indicia that indicate the alignment of the lamellae within the joint. In some embodiments, the implants comprise a plurality of implant elements, with the implant elements oriented so that the lamellae of the elements are aligned with each other. The implants can be inserted into a joint with the lamellae aligned across the joint to resist compression or deforming forces of the joint and to provide for improved implant strength. In some embodiments, the implants can be inserted into a joint over a pin and/or through a cannula to help guide the implant to the implant site within the joint. In some embodiments, the implants can be desirably formed from bone plugs harvested from long bones.

Abstract: A hip prosthesis includes a stem intended to be inserted in the neck of the femur, a prosthetic head shaped as a substantially hemispherical cup, intended to be inserted in the acetabular seat, a distal prosthetic component connected to the stem and shaped as a substantially hemispherical cup with concavity towards the concavity of the prosthetic head, and a ball disposed between the distal prosthetic component and the prosthetic head in such manner to generate a ball coupling, wherein the prosthetic head includes a flattened pole that defines an external central flat planar surface in order to adjust to various shapes of the acetabular seat, grooves externally obtained to be coupled with the acetabular seat and holes to receive screws that are screwed into the acetabular seat.

Abstract: Systems and methods for providing deeper knee flexion capabilities. In some instances, such systems and methods include a tibial component that has an asymmetrical articular plateau that includes a medial tibial condylar surface and a lateral tibial condylar surface. In some cases, at least one of the medial condylar surface and the lateral condylar surface includes a concave articulation surface having a lowest point that disposed from a posterior edge of the tibial component by between about 18% and less than about 35% of a total anteroposterior dimension of the tibial component. Other implementations are also discussed.

Abstract: 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.

Abstract: An endoprosthesis for knee joint arthrodesis having a femur portion including a femur attachment structure; a tibia portion including a tibia attachment structure; a coupling section formed on the femur portion and a coupling section formed on the tibia portion. The coupling sections are pivotably connected to one another about a prosthesis pivot axis that extends in the installed position of the endoprosthesis horizontally from medial to lateral. A locking element is moveable between locking and release positions. In the locking position the locking element rigidly locks the coupling sections in a predefinable pivot position. In the release position the coupling sections are pivotable relative to one another about the prosthesis pivot axis. A retaining and return means and an unlocking mechanism are provided. The retaining means forces the locking element into the locking position. The unlocking mechanism moves the locking element into the release position.

Abstract: Systems and methods for providing deeper knee flexion capabilities. In some instances, such systems and methods include a femoral component that is configured to replace a distal portion of a femur. In some cases, the femoral component comprises a first interior surface and a second interior surface that are each configured to contact a resected portion of the femur. Additionally, in some case, the first interior surface and the second interior surface are within about 20 degrees of being parallel with each other. Moreover, in some cases, the femoral component is configured such that when the femoral component is seated on the distal portion of the femur, the first interior surface runs at an angle between about 30 degrees and about 55 degrees with respect to a longitudinal axis of the femur. Other implementations are also discussed.

Abstract: The present invention provides a method and device for restoring individual patient joint kinematics using minimally invasive surgical procedures. The instrumentation of the invention sculpts the articular surface of a first bone that normally articulates in a predetermined manner with a second bone. The instrumentation includes a bone sculpting tool and a mount for attaching the tool to the second bone. The implant system is comprised of implants that 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.

Abstract: A modular humeral head resurfacing implant including a head, an anchoring stem, and a modular extended articulation flange. The head includes an exterior hemispherical articulating surface defining a terminating rim, an interior concave surface opposite to the exterior articulating surface, and a first coupling mechanism proximate to the terminating rim. The anchoring stem is coupled to the interior concave surface and extends along a stem axis that extends through an axial center of the head. The articulation flange includes a second coupling mechanism configured to cooperate with the first coupling mechanism to fasten the articulation flange to the head and an outer articulating surface that is curved along substantially its entire length and is substantially flush with the exterior hemispherical articulating surface when the articulation flange is fastened to the head.

Abstract: This set (J) comprises glenoid components (S1, S2, M1, M2, L1, L2) that each include a body (S1.1, S2.1, M1.1, M2.1, L1.1, L2.1) defining, on two of its opposite faces, respectively, a joint surface (S1.2, S2.2, M1.2, M2.2, L1.2, L2.2), intended to cooperate with a humeral head, and a bearing surface (S1.3, S2.3, M1.3, M2.3, L1.3, L2.3) bearing against the socket of a shoulder blade. In this set, the glenoid components are provided in several different sizes (S, M, L), respectively defined by the dimensions of the joint surface of their body. At least two glenoid components (S1 and S2, M1 and M2, L1 and L2) of which the bearing surfaces (S1.3 and S2.3, M1.3 and M2.3, L1.3 and L2.3) respectively have different dimensional geometries are provided so as to allow the surgeon to improve the durability of the mechanical cooperation between the implanted component and the operated socket.

Abstract: A surgical implant is provided with upper and lower telescoping members which move axially between extended and retracted positions. A fixed length sleeve fits over the telescoping members. The sleeve is load bearing to support axial loads. The sleeve also prevents the telescoping members from retracting and encloses an internal cavity within the implant for packing bone fusion material.

Abstract: An implant for therapeutically separating bones of a joint has two endplates each having an opening through the endplate, and at least one ramped surface on a side opposite a bone engaging side. A frame is slideably connected to the endplates to enable the endplates to move relative to each other at an angle with respect to the longitudinal axis of the implant, in sliding connection with the frame. An actuator screw is rotatably connected to the frame. A carriage forms an open area aligned with the openings in the endplates. The openings in the endplates pass through the carriage to form an unimpeded passage from bone to bone of the joint. The carriage has ramps which mate with the ramped surfaces of the endplates, wherein when the carriage is moved by rotation of the actuator screw, the endplates move closer or farther apart.

Abstract: A prosthesis for the replacement of multiple diseased or traumatized spinal facets comprises a portion that replaces at least a bony portion of the facets to be replaced and where the prosthesis attaches to the vertebra in a manner that does not require attachment to, or abutment against, the lamina. Multiple configurations of the prosthesis provide for replacement of the two inferior facets, the two superior facets, a superior and inferior facet, or all four facets. A method of installing the prosthesis is provided that is comprised of the steps of resecting at least a portion of the facets that carry the diseased or traumatized spinal facets and attaching the prosthesis in a manner that does not require attachment or abutment against the lamina.

Abstract: A lateral plate assembly has an elongated lateral plate for attachment to adjacent vertebrae having a first end portion and a second end portion and a pair of apertures for receiving a first and a second bone screw. The pair of apertures includes a first aperture which is an opening positioned in the first end portion for receiving the first bone screw and a second aperture which is a slotted opening to receive the second bone screw. The second end portion of the lateral plate has an open end with channelled internal sides for receiving and holding a moveable washer on top of the slotted opening. The washer is configured to move along a length of the slotted aperture. The moveable washer has an opening for holding a head of the second bone screw. Movement of the washer relative to the slotted opening increases or decreases the distance between locations of the respective screw heads.

Abstract: A prosthetic intervertebral disc and methods for using the same are provided. The subject prosthetic discs are characterized by including top and bottom endplates separated by a fibrous compressible element that includes an annular region and a nuclear region. The two plates are held together at least one fiber wound around at least one region of the top endplate and at least one region of the bottom endplate. The subject discs may he employed with separate vertebral body fixation elements, or they may include integrated vertebral body fixation elements. Also provided are kits and systems that include the subject prosthetic discs.

Abstract: A joint spacer therapeutically maintains separation of bones of a joint. A carriage is slideably retained within the frame and has at least one ramped surface. An actuator screw is threadably engaged with the frame, and rotatably connected to the carriage, to cause the carriage to slideably move within the frame when the actuator screw is rotated. First and second endplates engage the bones of the joint, and each has at least one ramped surface that is mateable with the ramped surface of the carriage, whereby when the carriage is slideably moved by rotation of the actuator screw, the endplates ramped surface slides against the carriage ramped surface to cause the endplates to move along an axis transverse to the longitudinal axis of the frame, to increase the height of the spacer. Piercing elements are connected to the carriage to pierce bone of the joint when the carriage is moved.

Abstract: A prosthetic intervertebral disc is formed of first and second end plates sized and shaped to fit within an intervertebral space and to be implanted from the back of the patient, thereby decreasing the invasiveness of the procedure. The posterior approach provides for a smaller posterior surgical incision and avoids important blood vessels located anterior to the spine particularly for lumbar disc replacements. The first and second plates are each formed of first, second and third parts are arranged in a first configuration in which the parts are axially aligned to form a low profile device appropriate for insertion through the small opening available in the TLIF or PLIF approaches described above. The three parts of both of the plates rotate and translate with respect to one another in situ to a second configuration or a deployed configuration in which the parts are axially unaligned with each other to provide a maximum coverage of the vertebral end plates for a minimum of insertion profile.

Abstract: A method of delivering a fusion cage to an intervertebral disc space bounded by adjacent vertebral endplates, comprising the step of delivering the fusion cage into the disc space without contacting its teeth to the vertebral endplates during delivery, wherein a sheath is interposed between a cage surface and the endplates to prevent contact therebetween during delivery.

Abstract: The present invention provides an intervertebral implant for implantation in a treated area of an intervertebral space between vertebral bodies of a spine. The implant includes a spacer portion having an inferior and superior surface, wherein the inferior and superior surfaces each have a contact area capable of engaging with anatomy in the treated area, and the inferior and superior surfaces define a through-hole extending through the spacer body. The present invention further provides screw holes extending from a side portion to the inferior and superior surfaces of the spacer portion and a plate portion rigidly coupled to the spacer portion through a coupling means, wherein the plate portion contains screws holes for receiving screws. A screw back out prevention mechanism adapted on the plate portion and prevents the back out of screws from the screw holes.

Abstract: Disclosed herein are methods, compositions and tools for repairing articular surfaces repair materials and for repairing an articular surface. The articular surface repairs are customizable or highly selectable by patient and geared toward providing optimal fit and function. 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.

Abstract: A bone fusion method, apparatus and device for insertion between bones that are to be fused together and/or in place of one or more of the bones, such as, for example, the vertebrae of a spinal column. The bone fusion device comprises one or more extendable plates having a central rib. The bone fusion device includes one or more support channels configured to receive an insertion instrument that is then secured to the bone fusion device via a coupling mechanism. As a result, the coupled device is able to be securely positioned between vertebrae using the insertion instrument with minimal risk of slippage.

Abstract: A patient specific glenoid guide is provided to facilitate properly aligned implantation of a glenoid prosthesis into a patient. The guide shape is designed preoperatively based on the unique configuration of the scapula of the patient. The guide orientation is chosen preoperatively based on one or more of the bone structure of the patient, the wear pattern of the patient's glenoid cavity, the anchoring means of the glenoid prosthesis, or other aspects.

Abstract: A hip joint navigation system is provided that includes a base having at least one channel disposed therethrough for receiving a pin for mounting the base to the pelvis. A mount feature is disposed on a top surface. A registration jig is configured to couple with the base and to engage anatomical landmarks. In some aspects, a patient specific jig system for hip replacement is provided including an engagement surface formed to closely mate to acetabular bone contours of a specific patient and a registration feature configured to be in a pre-determined orientation relative to an acetabulum the patient when the jig is coupled with acetabular bone contours of the specific patient. In other aspects, methods of using the systems are provided.

Abstract: Apparatus for locating an attachment position for a reconstructed anterior cruciate ligament on an attachment surface of a bone comprises locating means 51, 61 arranged to locate at least one reference surface 4 of the bone and guide means 53, 54 arranged to define the attachment position in two dimensions on the attachment surface relative to the reference surface.

Abstract: A powered leg prosthesis including a powered knee joint with a knee joint and a knee motor unit for delivering power to the knee joint, a powered ankle joint coupled to the knee joint including an ankle joint and an ankle motor unit to deliver power to the ankle joint, a prosthetic foot coupled to the ankle joint, a plurality of sensors for measuring a real-time input, and controller for controlling movement of the prosthesis based on the real-time input. In the powered leg prosthesis, at least one of the knee motor unit or the ankle motor unit includes at least one drive stage, where the drive stage includes a rotary element for generating torque and at least one looped element affixed around the rotary element and configured for transmitting the torque to another rotary element coupled to a joint to be actuated.

Abstract: A hollow tubulous composite structure and method for prosthetic limbs is described.

Abstract: A prosthetic device has a movable body and foot member with an end effector for contacting an external surface. A base body is coupled to a first joint of the foot member. A compliant linking member is disposed between a second joint of the foot member and a first joint of the moveable body. The compliant linking member can be a spring or flexible beam. A passive linking member is coupled between a third joint of the foot member and a third joint of the moveable body. An actuator is disposed between the base body and the second joint of the movable body. The actuator can be a motor with an extension member. The compliant linking member extends during roll-over phase. The actuator acts to assist with the extension of the compliant linking member during roll-over phase to aid with push-off phase in the gait cycle.

Abstract: A prosthetic system having a microprocessor-controlled socket evacuation device, and a method of retaining a prosthesis on the residual limb of an amputee using such an evacuation device are described herein. The evacuation device can include an electrically powered vacuum pump. The evacuation device can be operated in a manner that automatically adjusts the socket vacuum level to correspond to a determined activity level of a user. The microprocessor control can also limit operation of the evacuation device to certain determined portions of a user's gait cycle.

Abstract: A stent includes a tubular support structure extending from a distal end to a proximal end, the tubular support structure including an inner surface and an outer surface. A retractable anchor system is disposed relative to the tubular support structure and includes a frame member and a plurality of retractable anchors secured to the frame member. The plurality of retractable anchors are biased to a deployed configuration in which the plurality of retractable anchors extend radially outward from the outer surface of the tubular support structure but are radially inwardly compressible into a delivery configuration.

Abstract: This disclosure contains methods, devices, and systems for object removal from a body, including removal of a stent from a body. Some methods of the present disclosure include inflating a balloon on a catheter, engaging a stent with a socket defined by a surface of the balloon, the surface inwardly sloped toward a lumen of the catheter, and retracting a portion of the stent through the socket and into the lumen. The present disclosure also includes methods for making a catheter, including forming a balloon, inverting a portion of the balloon, and attaching the balloon to a catheter such that a surface of the balloon defines a socket that is inwardly sloped toward a lumen of the catheter.

Abstract: A deployment system for a self expanding stent includes a catheter assembly with a tip attached to a distal end segment of an elongate tube. The tip includes a proximal portion molecularly joined to a distal portion, which has a lower durometer hardness than the proximal portion. The proximal portion includes an anchor surface in contact with the distal portion, and oriented perpendicular to a central axis of the elongate tube. The elongate tube may be formed from a thermosetting polyimide, and the overmolded tip may be made from two different colored and different hardnesses of polyether block amide material. The tip is overmolded onto an untreated external surface of the elongate tube.

Abstract: A duet stent deployment system is used in a transjugular intrahepatic portosystemic shunt procedure. The device has a versatility of adjusting to a patient's anatomy in vivo. The system includes exactly two self expanding stents mounted on an inner catheter and covered by an outer sheath that is moved among a pre-deployment configuration, a first deployment configuration and a second deployment configuration to position the stents in an overlapping configuration from the portal vein, through a shunt and into the hepatic vein, and terminating at the junction with the vena cava.

Abstract: The present invention relates to a device having a hinged splint made up of a shank of the big toe (1) and a shank of the metatarsus (2) which have an articulated connection. Both shanks (1, 2) are fitted with bands (11, 12) fastening the hinged splint to the patient's foot. The articulated connection of the sharks (1, 2) comprises the first (4) and the second (5) cylindrical hinge. The cylindrical hinges (4, 5) are connected by means of a central element (3) of the hinged splint, with the axes of rotation (6) of both cylindrical hinges (4, 5) being substantially parallel to each other.

Abstract: An orthopedic device has various frame elements concealed by a sleeve defining pockets into which such frame elements are located. The orthopedic device includes a strap tightening assembly adapted to secure a plurality of straps simultaneously. The frame may include flexible edge features located along a periphery thereof.

Abstract: A foot sleeve is taught that has generalized sleeve compression from an elastic foot sleeve but also has targeted additional compression in the arch and above the heel across the Achilles tendon by a polymeric pressure sensitive adhesive tape applied as an X under the foot arch and in a preferred embodiment also across the Achilles tendon, just above the heel.

Abstract: An ankle brace includes a footplate with a lateral element, a medial element and an expandable element. The lateral element and the medial element of the footplate, which may be formed from a somewhat rigid material, are separate from one another and are spaced apart from one another. The expandable element is located between the lateral element and the medial element. It secures the lateral element and the medial element of the split footplate to one another. Braces and bracing systems that include the split footplate are disclosed, as are methods for supporting an individual's foot and/or ankle.

Abstract: A back plate of a waist support includes a plate body and two spring members. The plate body has a valley portion and two positioning holes. The two positioning holes are arranged symmetrically on the right and left sides of the valley portion. Each of the spring members is installed in the positioning hole of the plate body and provides a propping force to a wearer of the waist support. Thereby, the waist support can more effectively distribute the load that is otherwise focused on of the wearer's waist vertebra and in turn provides the wearer with more comfort.

Abstract: A thermoplastic cast, which is easy to reuse or implant, and a production method for same, are described. The cast includes a core material to which is attached polycaprolactone while being made in a mesh shape by the mutual crossing over and connecting of threads having a predetermined diameter, with the weaving of a plurality of strands of thin threads; and a structure which is made using a polycaprolactone composite and is formed so as to surround the outer part of the core material by means of insert injection. The patient experiences no discomfort despite the cast being structurally robust, because ventilation properties are improved due to the cast being formed in a mesh shape and because the structure, which is made using the polycaprolactone composite, is formed so as to surround the outer part of the core material by means of insert injection.

Abstract: The present invention provides an adhesive shoulder support apparatus that is simple in design and which can he easily applied by the user between the shoulder and the adjacent deltoid without requiring the consultation or application of taping to be performed by a physician or physical therapist. The adhesive shoulder support apparatus of the present invention is formed of a stretchable and breathable material that provides sufficient structural tension and support to a shoulder of a user so as to contribute to proper alignment and, accordingly, facilitate a reduction or elimination of shoulder pain caused by core workouts, sports fatigue or injuries, while at the same time promoting healing. A shoulder support apparatus of the present invention comprises a single adhesive member being formed of a durable, resilient material having an adhesive backing.