134 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.

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 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.

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.

This intraocular lens includes an optic body having anterior and posterior walls, a chamber, and optically transmissive primary and secondary fluids, and method for making and using the same. The secondary fluid is substantially immiscible with the primary fluid and has a different density and a different refractive index than the primary fluid. The primary fluid is present in a sufficient amount that orienting optical body optical axis horizontally for far vision positions the optical axis through the primary fluid, thereby immersing the anterior and posterior optical centers in the primary fluid. The secondary fluid is contained in the optic body in a sufficient amount that orienting the optical axis at a range of effective downward angles relative to the horizontal for near vision positions the optical axis to extend through the primary fluid and the secondary fluid, thus changing the focus of the intraocular lens.

A surgical instrument for treating female pelvic prolapse comprising a mesh sling for implanting into the pelvis of a female, which provides support to the urethra, the anterior vaginal wall, and the posterior vaginal wall with the sling defining a tissue-anchoring segment attached to opposite ends of the mesh sling. The mesh sling is surgically positioned using a tissue anchor applier instrument. The tissue anchor segment is positioned to attach to durable fascia that is located anatomically to support the sling. The durable fascia anchored vaginal wall support sling is positioned to provide support to the urethra for surgical management of female urinary incontinence, support to the anterior vaginal wall for surgical management of female cystocele, and support to the posterior vaginal wall for surgical management of female rectocele.

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.

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.

A mesh delivery system (2) for sacral colpopexy procedures is disclosed. The system (2) uses a mesh stabilizer (30), an endoscopic introducer (2) that carries the mesh stabilizer (30) into the abdomen, and a vaginal probe (10) (inserted through the vagina) with a head that interfaces with the mesh stabilizer (30) in lock-and-key fashion. The mesh stabilizer (30) delivers mesh straps for sacral colpopexy into the abdomen. After delivery, the stabilizer (30) interfaces with the probe (10) head and locks the mesh stabilizer (30) with mesh straps in place. The endoscopic introducer (20) can then be temporarily detached and removed to facilitate suturing of the mesh to the anterior and posterior vaginal walls. After permanent suturing, the introducer (20) can be reinserted and used to retrieve the mesh stabilizer (30) component.

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 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.