140 results about "Anterior wall" patented technology

A vertebral cage is provided for use in preserving the space between adjacent vertebral during the process of spinal fusion. In particular, this cage has an open modified oval peripheral shape with a continuous fluid anterior wall having angled screw passages accessible through co-planar openings to allow the construct to be stabilized between adjacent vertebral bodies through their endwalls. In addition, the cage has a back to front wedge taper with pull-out resistant ratchet surfaces. Further, in a second aspect of the invention, the screw passages have a unique locking mechanism provided by oversized internal threads in combination with a second locking thread on the head of the associated bone screws that allows for axial translation of the screws within the screw passages. This in turn permits play in the angulation of the screw relative to the anchoring bone in order to optimize the screw placement in the bone.

According to some embodiments, a method for promoting spinal fusion using a spinal implant comprises providing a spinal implant, wherein the spinal implant comprises an anterior wall, a posterior wall and two lateral walls configured to extend between the anterior wall and the posterior wall. In some embodiments, the spinal implant further comprises at least one internal chamber generally positioned between the anterior wall, the posterior wall and the two lateral walls, wherein the internal chamber being is adapted to receive at least one graft and / or other fill material. In some arrangements, the anterior wall of the spinal implant comprises at least one opening or hole that places the internal chamber in fluid communication with an exterior area or portion of the spinal implant. In one embodiment, at least one of the two lateral walls comprises an access port. The method additionally includes positioning the spinal implant between two adjacent vertebrae of a patient and directing at least one graft and / or other fill material into the internal chamber of the spinal implant through the access port. In some embodiments, at least a portion of the graft and / or other fill material delivered into the internal chamber is configured to exit through the one or more of the openings of the anterior wall.

An angled fixation device, such as an angled screw. This angled fixation device may be used by the surgeon to secure a spacer to a spinal disc space. The proximal end portion of the angled fixation device is driven perpendicular to the anterior wall of the spacer, and so is parallel to the vertebral endplates and in-line with the inserter. The distal end portion of the angled fixation device is oriented at about a 45 degree angle (plus or minus 30 degrees) to the vertebral endplate it enters.

A banana shaped intevertebral fusion cage having a domed profile, an internal planar wall defining first and second graft chambers, asymmetrically disposed leading and trailing insertion, and an anterior wall recess.

A preformed, seamless, three-dimensional, anatomically contoured prosthetic device for reinforcing breast tissue and supporting a breast implant includes a flat back wall, a concave front wall and a curved transitional region between the flat back wall and the front wall defining a smoothly curved bottom periphery. A concave receiving space is defined by the back wall and the front wall for at least partially receiving and supporting the breast implant therein. The three-dimensional prosthetic device is free of wrinkles, creases, folds or seams, which may have otherwise caused potential tissue irritation, bacteria hosting, infection and palpability problems.

Gastric volume of a patient is reduced by deploying an endoscope into a stomach through the esophagus. A plurality of anterior anchors are affixed to the anterior wall of the stomach. The anterior anchors are distributed along an anterior line of the stomach wall beginning near the cardia region and extending toward the stomach exit. A plurality of posterior anchors are affixed to the posterior wall of the stomach. The posterior anchors are distributed along a posterior line of the stomach wall beginning near the cardia region and toward the stomach exit. The anchor line and the stomach wall are drawn towards the posterior line of the stomach wall to reduce gastric volume.

A method, and related tools for performing the method, of delivering a stent or other like device to the heart to connect the left ventricle to the coronary artery to thereby supply blood directly from the ventricle to the coronary artery may be used to bypass a total or partial occlusion of a coronary artery. The method may include placing a guide device and a dilation device through an anterior wall and a posterior wall of the coronary vessel and through a heart wall between the heart chamber and the coronary vessel. The dilation device may be used to form a passageway in the heart wall at a location defined by the guide device. The method may then include placing a stent within the passageway.

One embodiment of a hollow spinal spacer (10) includes a curved anterior wall (11) having opposite ends (12, 13), a posterior wall (15) having opposite ends (16, 17), two lateral walls (20, 21), each integrally connected between the opposite ends (12, 13, 16, 17) of the anterior (11) and posterior (15) walls to define a chamber (30). The walls (11, 15, 20, 21) include a superior face (35) and an inferior face (40). The superior face (35) defines a first opening (36) in communication with the chamber (30) and includes a first vertebral engaging surface (37). The inferior face (40) defines a second opening (41) in communication with the chamber (30) and includes a second vertebral engaging surface (42).

A preformed, seamless, three-dimensional, anatomically contoured prosthetic device for reinforcing breast tissue and supporting a breast implant includes a flat back wall, a concave front wall and a curved transitional region between the flat back wall and the front wall defining a smoothly curved bottom periphery. A concave receiving space is defined by the back wall and the front wall for at least partially receiving and supporting the breast implant therein. The three-dimensional prosthetic device is free of wrinkles, creases, folds or seams, which may have otherwise caused potential tissue irritation, bacteria hosting, infection and palpability problems.

A vascular valve constructed from a biocompatible material that is designed to be surgically implanted in a patient's blood vessel, such as the right ventricular outflow tract. At the first end of the valve there is an orifice defined by at least two opposing free edges, and which can occupy either a first, closed position or a second, open position. At the second end of the valve there are at least two flexible members attachable to an anterior and a posterior wall of a patient's blood vessel. A length of the orifice between said at least two opposing free edges when the orifice is generally closed is equal to about 1.5 to 2 times the diameter of a patient's blood vessel. Optionally, the two flexible members to a stent or tubular graft. The valved stent or tubular graft can be inserted into a patient's blood vessel or heart.

A patient interface for delivery of a supply of pressurised air or breathable gas to an entrance of a patient's airways includes a frame member, a cushion assembly provided to the frame member, and an anterior wall member repeatedly engageable with and disengageable from the cushion assembly. The frame member includes connectors operatively attachable to a positioning and stabilizing structure. The cushion assembly includes a seal-forming structure and a void defined by an anterior surface of the cushion assembly. The anterior wall member has a predetermined surface area to seal the void of the cushion assembly and form a gas chamber when the anterior wall member and the cushion assembly are engaged. The void of the cushion assembly is sized such that the patient's nose and / or mouth is substantially exposed when the anterior wall member is disengaged from the cushion assembly thereby improving breathing comfort of the patient.

A precisely size matched intervertebral plate and spacer assembly for ensuring a tight fit within a disc space to promote spinal fusion, comprising: a “U-shaped” spacer configured to fit within the intervertebral space; and, a matching countersunk low profile “H-shaped” anterior plate joined perpendicularly to the spacer. The plate further comprises: a plurality of anchor members configured to attach to the junctions of the anterior cortex faces and the endplates; and, channels individually traversing through the anchor members for inserting screws into the vertebral bodies' cortical bone. The spacer comprises a hollow three-sided U-shaped member, comprising two opposing parallel side walls, and a perpendicular posterior wall, while lacking a superior, inferior, and anterior wall. The exterior walls of the plate and spacer are planar, while the interior walls of the spacer are curved to house a precisely fitting cylindrical graft, or other insert such as DBM, bone dust, bone paste, bone dowel with direct contact to the endplates to promote fusion.

Prosthetic liner formed of a molded silicone elastomer material including an inner wall, a circular outer wall having radii of curvature centered along a first longitudinal axis of external symmetry extending longitudinally centrally within the liner, the inner wall including a circular curved inside anterior wall portion extending along a liner length and having first radii of curvature centered on a second longitudinal axis of anterior curvature extending longitudinally along the liner length and a circular curved inside posterior wall portion having a second radii of curvature centered on a third longitudinal axis of posterior curvature extending along said liner length. The first, second and third longitudinal axes lie in a common longitudinally and transversely extending plane bisecting the anterior and posterior wall portions, and the second and third axes are spaced apart a predetermined offset distance on opposed sides of the first axis to thereby define an anterior wall portion that is thicker along the liner length than the posterior portion.

According to some embodiments, a method for promoting spinal fusion using a spinal implant comprises providing a spinal implant, wherein the spinal implant comprises an anterior wall, a posterior wall and two lateral walls configured to extend between the anterior wall and the posterior wall. In some embodiments, the spinal implant further comprises at least one internal chamber generally positioned between the anterior wall, the posterior wall and the two lateral walls, wherein the internal chamber being is adapted to receive at least one graft and / or other fill material.

A custom mouthguard has a resilient U-shaped body with an anterior wall and a posterior wall. A post dam on the posterior wall forms a seal with palatal tissue to increase retention of the mouthguard in a wearer's mouth. The increased retention allows a wearer to speak and open mouth breath while wearing the mouthguarrd. The mouth guard also has an indexed region that serves to mutually stabilize maxillary teeth, mandibular teeth, mandible and TMJ components. Mouthguard methods and processes are also disclosed.

An improved body element for use in a modular prosthetic stem component of the sort comprising a body element and at least one other element, wherein the body element and the at least one other element are joined together by at least one modular connection, wherein the improved body element comprises an anterior wall and a posterior wall, at least one of the anterior wall and the posterior wall converging toward the other on the medial side of the body element and diverging away from the other on the lateral side of the body element, whereby the body element approximates a general wedge shape.

Fixation systems, kits and methods for vertebral interbody fusions are provided. The fixation systems fix an intervertebral cage in the spine to resist left to right rotation, flexion and / or extension. In one embodiment, the fixation system contains two keels that are insertable into an attachment portion or an anterior wall of an intervertebral cage. Each keel contains a blade with two flanges, in the shape of half of an I-beam. The attachment portion may be one or more pieces that mate to form the attachment portion, such as an I-beam attachment portion. The blades can be straight or curved. Preferably the fixation systems are modular, allowing for parts to be interchanged to suit the patient's needs. The fixation systems may be provided in a kit, preferably with more than two keels having different sizes and / or shapes, more than one cage, and / or more than one attachment portion.

Conduits are provided to direct blood flow from the left ventricle to a coronary artery at a location distal to a blockage in the coronary artery. Threaded and nonthreaded conduits are delivered using a guidewire delivered through the posterior and anterior walls of a coronary artery and into the heart wall. A dilator may be provided over the guidewire into the heart wall, and the conduit delivered over the dilator. An introducer sleeve may be provided over the dilator into the heart wall, the dilator removed, and the conduit delivered through the introducer sleeve. A hollow needle also may be inserted into the posterior and anterior walls of the coronary artery prior to inserting the guidewire. A depth measuring tool may determine the appropriate length of the conduit prior to delivery. The depth measuring tool can include the hollow needle with an access port on a proximal end of the needle and an opening on the distal end of the needle in flow communication with the access port so that when the needle is inserted through the heart wall and into the heart chamber, blood flow through the opening.

An oral appliance includes a reinforcing member or splint embedded within a polymer shell. The reinforcing member or splint includes an anterior portion embedded within an anterior wall of the polymeric shell, a posterior portion embedded within a posterior wall of the polymeric shell, and a transverse portion embedded within a transverse plate of the polymeric shell. The reinforcing member or splint is operative for preventing movement of the user's dentition over time when wearing the oral appliance.

The invention discloses a stent-type blood vessel for the intracavity treatment of a complex abdominal aortic aneurysm, which comprises a main body stent and branch stents. The main body stent is funnel-shaped. Two front wall windows are arranged on the front wall of the upper part of the main body stent and two side wall windows are arranged on the side wall of the middle part of the main body stent. Straight tube stent-type blood vessel passages are respectively and upwards arranged on the side wall windows. Each branch stent is circular-tube-shaped and the thickness of the branch stent is adaptive to the diameter of a renal artery.

An angled fixation device, such as an angled screw. This angled fixation device may be used by the surgeon to secure a spacer to a spinal disc space. The proximal end portion of the angled fixation device is driven perpendicular to the anterior wall of the spacer, and so is parallel to the vertebral endplates and in-line with the inserter. The distal end portion of the angled fixation device is oriented at about a 45 degree angle (plus or minus 30 degrees) to the vertebral endplate it enters.

The invention discloses an implant. The implant may include a first flap and a second flap. The first flap may further include a first portion, a second portion and a transition region. The first portion may be configured to be attached proximate a sacrum. The second portion may be configured to be attached to an anterior vaginal wall. The transition region lies between the first portion and the second portion. The second flap may be fabricated such that a portion of the second flap is configured to be attached to a posterior vaginal wall. The implant may be configured such that a value corresponding to a biomechanical parameter defining a biomechanical attribute of the portion of the first flap attaching to the anterior wall is different from a value of the biomechanical parameter defining the biomechanical attribute of the portion of the second flap attaching to the posterior wall.

An ultrasound system and method to measure an organ wall weight and mass. When the organ is a bladder, a bladder weight (UEBW) is determined using three-dimensional ultrasound imaging that is acquired using a hand-held or machine controlled ultrasound transceiver. The infravesical region of the bladder is delineated on this 3D data set to enable the calculation of urine volume and the bladder surface area. The outer anterior wall of the bladder is delineated to enable the calculation of the bladder wall thickness (BWT). The UEBW is calculated as a product of the bladder surface area, the bladder wall thickness, and the bladder wall specific gravity.