Abstract:
A reinforced graft construct for repairing a tendon or ligament formed by inserting a piece of material, such as suture, through the graft lengthwise. The material may be inserted along only a portion of the graft or along the entire graft. The material may be a reinforcement (reinforcing) material such as suture, tape, weave, or mesh passed lengthwise through the graft (for example, along the center of the graft). The ends of the graft may be whipstiched to provide additional fixation when implanted. The material may be bioabsorbable such that it will resorb away after a period of time in the body.
Abstract:
A medical device according to the present invention is to be arranged in a lumen of a gastrointestinal tract. The medical device includes: at least one cylindrical part which is opened at least one end thereof; and at least one attachment part which is arranged on at least one portion of the cylindrical part and is configured such that the medical device is attachable to the lumen of the gastrointestinal tract. The cylindrical part is configured to be arrangeable along at least one portion of the gastrointestinal tract, and at least one portion of a side surface of the cylindrical part is configured to be followable to a shape of an inner wall of the gastrointestinal tract.
Abstract:
A method of implanting a penile prosthetic includes confirming that a tow suture is coupled with a resorbable suture-engagement component attached to an exterior surface of a cylinder. The method includes inserting the tow suture into a corpora cavernosum of a penis and pushing the tow suture through a glans of the penis and pulling on the tow suture and towing the cylinder to a distal location within the penis. The tow suture is removed from the resorbable suture-engagement component.
Abstract:
A vascular filter includes filtration struts formed between a hub and a supporting stent structure including stent struts. The hub and the filtration basket are formed from a material that is more biodegradable that the material from which the supporting stent structure is formed. The vascular filter is laser cut from an intermediate tube.
Abstract:
The present invention relates to a prosthesis (100) comprising an openworked three-dimensional knit (101) comprising a front face and a rear face, each face being formed with one or more laps of yarns defining pores on said face, the front face being bound to the rear face by connecting yarns defining a spacer, characterized in that the connecting yarns are distributed so that they define an entanglement of yarns crossing each other at the spacer, without obstructing the pores of the front and rear faces.
Abstract:
The present invention generally relates to the field of prostheses for surgical applications, to methods of their manufacturing and to methods of treating a patient by implanting them into a patient. More particularly, the present invention relates to prostheses having a multi-layered sheet structure and their use in hernia repair, the repair of anatomical defects of the abdominal wall, diaphragm, and chest wall, correction of defects in the genitourinary system, and repair of traumatically damaged organs such as the spleen, liver or kidney.
Abstract:
Described are methods, devices, and systems related to implants for the treatment of a female pelvic condition. The implants include absorbable and non-absorbable materials and can be introduced into the pelvic area transvaginally. Meshes of the invention provide benefits relating to improved tissue integration into the mesh, reduced infection likelihood, improved patient comfort following implantation, or combinations of thereof.
Abstract:
The present invention provides a system and method for gender specific medical treatment. The medical treatment system can include gender specific medical devices which are designed to account for the anatomical and physiological differences in the male and female genders. The medical treatment system can also include a medical device identification system which differentiates use for male and female patients. The medical device identification system includes a container adapted to receive a medical device and a gender specifier. The gender specifier is used to identify the gender the medical device in designed for. The gender specifier can be in text form, symbolic form, or color coded.
Abstract:
A urethral scaffold is provided for expanding a portion of the urethra that extends through the prostate. The scaffold is expandable and has a plurality of undulating circumferential members disposed between a proximal end and a distal end of the scaffold. A central section of the scaffold has a width that exceeds the width at the distal end of the scaffold. The scaffold is made of a material that reacts with urine or with tissue surrounding the urethra to reduce the volume of the scaffold such that the scaffold can self-explant without an interventional procedure.