904 results about "Fascia" patented technology

Methods and apparatus for implanting a stimulation lead in a patient's sacrum to deliver neurostimulation therapy that can reduce patient surgical complications, reduce patient recovery time, and reduce healthcare costs. A surgical instrumentation kit for minimally invasive implantation of a sacral stimulation lead through a foramen of the sacrum in a patient to electrically stimulate a sacral nerve comprises a needle and a dilator and optionally includes a guide wire. The needle is adapted to be inserted posterior to the sacrum through an entry point and guided into a foramen along an insertion path to a desired location. In one variation, a guide wire is inserted through a needle lumen, and the needle is withdrawn. The insertion path is dilated with a dilator inserted over the needle or over the guide wire to a diameter sufficient for inserting a stimulation lead, and the needle or guide wire is removed from the insertion path. The dilator optionally includes a dilator body and a dilator sheath fitted over the dilator body. The stimulation lead is inserted to the desired location through the dilator body lumen or the dilator sheath lumen after removal of the dilator body, and the dilator sheath or body is removed from the insertion path. If the clinician desires to separately anchor the stimulation lead, an incision is created through the entry point from an epidermis to a fascia layer, and the stimulation lead is anchored to the fascia layer. The stimulation lead can be connected to the neurostimulator to delivery therapies to treat pelvic floor disorders such as urinary control disorders, fecal control disorders, sexual dysfunction, and pelvic pain.

The invention relates to a surgical instrument and a method for treating female urinary incontinence. A tape or mesh is permanently implanted into the body as a support for the urethra. In one embodiment, portions of the tape comprise tissue growth factors and adhesive bonding means for attaching portions of the tape to the pubic bone. In a further embodiment, portions of the tape comprise attachment means for fastening portions of the tape to fascia within the pelvic cavity. In both embodiments the tape is implanted with a single incision through the vaginal wall.

A balloon device useful for dissecting tissue or retracting tissue for the purpose of providing access for laparoscopic surgery, the device comprising a balloon which inflates to a shape specially suitable for the surgical procedure and the anatomical region of deployment. The present device, when configured with a tapered dissection balloon, is particularly useful for subfascial endoscopic perforator surgical procedures.

A system for securing an implantable apparatus to a mammal includes a mount including a base portion having a plurality of holes dimensioned to receive rotationally-driven fasteners, each fastener comprising a helical portion having a tip configured for tissue penetration, the mount configured to secure the implantable apparatus relative to tissue of the mammal upon driving the fasteners into the tissue. The system further includes a fastening tool configured to rotationally drive the helical portion of the fasteners into the tissue. The mount may be secured to the fascia covering the sternum via a subcutaneous securement method, or it may be attached to the intra-abdominal wall, behind the sternum, or it may be attached to the sternum directly via bone screws or the like.

A method of implanting an injection port using the step of providing an injection port having a housing having a body, a fluid reservoir, a needle penetrable septum, and at least one stabilizing element mounted to the housing comprising a member having an undeployed position and a deployed position, wherein the stability element extends radially from the body. The method further involves the step of creating a surgical incision through the skin and subcutaneous fat layers of the patient to expose the fascia, and placing the injection port between the subcutaneous fat layer and the fascia tissue. The method even further involves the step of deploying the stability element.

A method and apparatus are provided for treating connective tissue. The method and apparatus includes elongating connective tissue including septa and/or fascia to achieve a lasting improvement (e.g., a long term, durable and/or substantially irreversible treatment of the connective tissue) to improve the appearance of cellulite.

Various methods and devices for minimally invasive treatment and prevention of conditions of the fascia are provided. In one aspect, a method includes providing an acoustic wave source effective to deliver a focused acoustic wave to a target site within a patient's body, and focusing an acoustic wave through a patient's skin such that at least one location in the patient's fascia is fenestrated in a desired pattern.

Surgical instruments, guides, and methods for closure of fascia and other tissue sites are disclosed. A suture passer guide comprises an elongate body with first and second passages for guiding a suture passer. The long axes of the elongate body, the first passage, and the second passage, preferably lie in three separate parallel planes. A suture passer comprises a housing having a needle tip portion and a first suture grasping surface. An elongate body is located at least partially within the housing and is configured to slide within the housing. The elongate body has a second suture grasping surface at the distal end. The first and second suture grasping surfaces preferably are spaced from the needle tip portion.

A surgical instrument, guide, and method capable of being used for closure of peritoneum fascia, occlusion of bleeding vessels such as inferior epigastric, and for all uses related to accurately passing suture material through a guide into tissue. A tip of a surgical instrument in a standard suture-/needle-driving position with a sharp tip that opens and closes with the surgeon grasping suture material with the sharp tip is provided. Insertion of the tip/suture through tissue until the tip is seen through the peritoneum by direct vision begins the wound-closing procedure. The suture is released by opening and withdrawing the tip from the guide. The suture is recovered by using the guide to redirect the tip and puncturing the tissue opposite the first point of insertion. The tip grasps the suture and pulls the suture through the guide. The suture is pulled outside the wound, providing for rapid closure of the surgical incision. The guide is insertable within the wound to be closed and guides the surgical instrument at a predetermined angle from the longitudinal axis of the guide for optimum wound closure. Alternative embodiments of the guide include providing a slot through which non-linear surgical instruments may pass through an open or enclosed passageway.

An anterior implant adapted to treat central and lateral cystoceles present in a female patient includes laterally extending stabilizing straps for supporting the implant between the patient's bladder and vagina independently of the patient's arcus tendineous fascia pelvis. Rectocele and hysterocele repairs can be carried out using a single posterior implant which, like the anterior implant, is provided with laterally extending stabilizing straps for supporting the implant between the patient's rectum and vagina.

A removable magnetic dental appliance is provided. The magnetic dental appliance can be used in the treatment of various conditions, including but not limited to, snoring, sleep apnea, some forms of temporomandibular joint pain or inflammation, myofascial pain or bruxism. The appliance comprises an upper arch attachment member and a lower arch attachment member, each for removably engaging at least a portion of the dentition. A magnetic component is positioned anteriorly on one of the upper arch attachment member or the lower arch attachment member and a magnet-attracted element is provided on the other arch attachment member for magnetic engagement with the magnetic component when the upper and lower arch attachment members are substantially vertically aligned. The appliance uses magnetic force to selectively position the mandible while still permitting movement of the mandible relative to the maxilla for improved comfort. A use of the magnetic dental appliance and a kit comprising the magnetic dental appliance are also provided

A boot for use in the treatment of plantar fasciitis. The boot places the foot in the desired amount of dorsiflexion, preferably from 5° to 20°, which stretches the Achilles tendon and is believed to prevent the shortening of the plantar fascia. The boot also provides protection for the foot while walking or engaging in other load bearing activities, to minimize further damage to and/or inflammation of the plantar fascia. The boot has a sole that is shaped to allow as close to a natural walking gait as possible while maintaining the foot in the desired degree of dorsiflexion. Preferably, the amount of dorsiflexion of the foot is controlled through the addition wedges on the base of the boot.

A method for internal fixation of vertebra of the spine to facilitate graft fusion includes steps for excising the nucleus of an affected disc, preparing a bone graft, instrumenting the vertebrae for fixation, and introducing the bone graft into the resected nuclear space. Disc resection is conducted through two portals through the annulus, with one portal supporting resection instruments and the other supporting a viewing device. The fixation hardware is inserted through small incisions aligned with each pedicle to be instrumented. The hardware includes bone screws, fixation plates, engagement nuts, and linking members. In an important aspect of the method, the fixation plates, engagement nuts and linking members are supported suprafascially but subcutaneously so that the fascia and muscle tissue are not damaged. The bone screw is configured to support the fixation hardware above the fascia. In a further aspect of the invention, a three component dilator system is provided for use during the bone screw implantation steps of the method.

A human body partial manikin having the same flexibility, elasticity, and texture as the human body is provided. And a manikin which has a feeling when it is cut open by means of a scalpel or scissors, similar to a feeling when an actual operation is performed by using a human body and is optimum for the anatomical practice of an inguinal hernia is provided. Accordingly, the human body partial manikin includes a skin portion which represents a skin layer on the surface of a lower abdomen of a human body, an abdominal external oblique muscle portion, an abdominal internal oblique muscle portion, a transverse abdominal muscle portion, a fascia transversalis portion, a fascia extraperitoneal portion, a peritoneum portion, and an abdominal cavity portion toward the inside of the manikin, wherein these respective portions are formed of a silicone resin.

A prosthesis for repairing a hernia includes an adhesion-resistant biodegradable region and an opposing tissue-ingrowth biodegradable region. When the prosthesis is implanted into the patient, the adhesion-resistant biodegradable region covers a fascial defect of the hernia, and the tissue-ingrowth biodegradable region is located above the adhesion-resistant biodegradable region while being exposed substantially only to the host's subcutaneous tissue layer. This orientation allows the tissue-ingrowth biodegradable region to become firmly incorporated with the host's body tissue. The adhesion-resistant biodegradable region faces the internal organs and decreases the incidence of adhesions and/or bowel obstruction.

An artificial body wall is disclosed herein. The artificial body wall may include a first layer and a second layer. The first layer is substantially formed of a silicone rubber and includes at least one of an artificial epidermis-dermis layer or an artificial subcutaneous layer. The second layer extends along and below the first layer and is substantially formed of a silicone rubber. The second layer includes at least one of an artificial fascia layer or an artificial muscle layer. At least one of the first layer or second layer may be vascularized.

A method and adjustable apparatus for stabilizing and strengthening the shoulder muscles and rotator cuff provides an active range of motion activities that can be performed with or without resistance. In particular, the method and apparatus provide for scapular retraction and protraction, shoulder flexion, extension, adduction and abduction, as well as internal and external shoulder rotation, performed horizontally and vertically. All of these motions are beneficial to the shoulder joint because they allow the joint to move freely throughout its normal range of motion using natural mechanics of the rotator cuff and surrounding muscles. The method and apparatus provide the essential benefit of stabilizing the shoulder and rotator cuff throughout these motions so that the user's range of motion and strength building is optimized. The method and apparatus also provide for self myofascial release techniques to decrease spasm.