Abstract: An adjustable nasal dilation device including a first deformable body having one or more ribs able to engage opposing internal sides of a nasal cavity wall when in position and an adjustment member which expands the first deformable body to enlarge the nasal cavity.
Abstract: The present invention provides an implantable prosthesis and more specifically, an implantable tubular textile prosthesis comprising a biocompatible fabric having inner and outer surfaces and first and second ends; the fabric having a textile construction comprising cold drawn PTFE yarns having a substantially uniform denier and high molecular orientation. Use of cold drawn PTFE yarns result in implantable prostheses that have excellent abrasion resistance, strength and lubricity properties. Useful textile constructions include weaves, knits, braids, filament windings, spun windings and combinations thereof. The prostheses of the present invention are lubricious and have characteristics that closely resemble the properties of a natural body lumen.
Abstract: A minimally invasive hip replacement surgical procedure that is also tissue preserving is disclosed. By making a superior incision, rather than a posterior incision, neither the posterior hip capsule, nor the gluteus medius or minimus are dissected. This results in improved post-operative results in the form of less dislocations and better healing.
Abstract: Lancet device that includes a body. A trigger is mounted to the body. A front cover has a skin engaging end that includes a lancet opening through which a lancet needle extends. A holding member is movably mounted within the body and includes a front end a rear end. The front end can be configured to receive a lancet. A stop surface moves with the holding member. A cam wheel includes cam surfaces which can be contacted by the stop surface. The cam wheel is configured to rotate at least partially. The cam wheel rotates about an axis that is parallel to an axis running through at least one of the lancet opening and the holding member.
Abstract: A tubular prosthesis device for use within the body. The device includes, a metal filament material formed of metal outer member having an exposed outer surface and a core within the extended outer member formed of a different metal than the outer member. The core is secured within and substantially enclosed by the outer member. The device can be reduced to a small size for introduction into the body lumen and expandable to a sufficiently large size to engage the wall of the body lumen. Stents formed of composite wires are shown.
Abstract: A method of minimally invasively reducing a volume of a hyper-inflated target section of diseased lung comprising the steps of introducing a bronchoscope into a patient's airway to a position adjacent the target section and equilibrating air within the target section with atmospheric air to at least partially deflate the target lung section; injecting an inflammation-causing substance into the target section to precipitate adhesion of the walls within the target lung section, preventing substantial re-inflation of the target section by occluding an airway upstream of the target section for a period of time, and removing the airway occlusion after the target section has substantially permanently been reduced in volume. The injected substance can be autologous blood or a constituent thereof.
Abstract: A fixation band for affixing a prosthetic heart valve to tissue, the fixation band comprising: a structure having a proximal end and a distal end in opposition to one another, and a lateral region between the proximal end and the distal end, wherein the prosthetic heart valve is attached to one of the proximal end and the distal end of the structure; a plurality of barbs selectively configurable between a first position and a second position, the barbs being contained within a peripheral boundary of the lateral region of the structure in the first position, and the barbs being extended from the peripheral boundary of the lateral region of the structure in the second position; and an actuator for selectively moving the plurality of barbs between the first position and the second position.
Type:
Grant
Filed:
April 16, 2003
Date of Patent:
August 29, 2006
Assignee:
Medtronic, Inc.
Inventors:
Steven B. Woolfson, Richard B. Streeter, Daniel C. Taylor, John R. Liddicoat
Abstract: An expandable stent having a proximal end and a distal end in communication with one another, and a tubular wall disposed between the proximal end and the distal end. The tubular wall has a longitudinal axis and a porous surface defined by a plurality of intersecting members comprising a series of longitudinal struts disposed substantially parallel to the longitudinal axis of the stent. Each longitudinal strut in the series comprises flexure members for substantially complementary extension and compression of a diametrically opposed pair of the longitudinal struts upon flexure of the stent. The flexure members may comprise first and second curved sections which are of a different size. At least one of the curved sections may comprise an arc of greater than about 180°.
Abstract: A device for treating spasmodic dysphonia (SD) and a surgical method of treating SD with use of the same are disclosed. The cause for SD is an excessively tight closure of the glottis. The device of the present invention is useful one for the surgery of thyroplasty type II which aims at widening the glottis. Use of the device may make the surgery easier, simpler, and shorter in time required.
Abstract: The invention provides tissue graft compositions comprising collagen-based extracellular matrices derived from renal capsules of warm-blooded vertebrates. The invention further provides a process of harvesting and purifying a renal capsule to provide an extracellular matrix material having beneficial use as a tissue graft and/or cell growth material.
Type:
Grant
Filed:
June 28, 2002
Date of Patent:
August 8, 2006
Assignee:
Cook Biotech Incorporated
Inventors:
Umesh H. Patel, Michael C. Hiles, Jason P. Hodde
Abstract: New tubular vascular implants (stents) that consist of biocompatible, thermoplastic material that have a shape memory and that contain at least one active ingredient are described. In addition, a process for their production and their use as vascular implants for prophylaxis of restenosis are described.
Type:
Grant
Filed:
November 21, 2001
Date of Patent:
August 8, 2006
Assignee:
Schering AG
Inventors:
Gesine Hildebrand, Johannes Tack, Helmut Kaeufer, Hans-Martin Wache, Thomas Mueller, Peter Ewert
Abstract: A prosthetic knee joint including stance-phase control means comprising lock or latch for holding the knee in a straight condition, and means determining the status of the latch, said status determining means defining a control axis located so that the lock or latch is activated when a load imposed on the joint passes through a line posterior to said axis, and is de-activated when the load passes through a line anterior to said axis.
Type:
Grant
Filed:
November 18, 2004
Date of Patent:
August 8, 2006
Assignee:
Bloorview MacMillan Centre
Inventors:
Jan Andrysek, Stephen Naumann, William L. Cleghorn
Abstract: A barbed medical prosthesis is disclosed in which the barb includes a basal portion comprising a point of union with the substrate of origin (such as a strut), an anchoring portion adapted to embed into tissue, and a stress-dispersing portion located between the basal and anchoring portions. In one embodiment the stress-dispersing portion comprises a helical coil having a free winding that is unattached to the strut from which the barb extends. In another embodiment, the stress-dispersing portion comprises a series of bends or curves formed in the barb proximate to the point of union with the strut. The barb can be mechanically attached and/or soldered to the prosthesis, or integrally formed therefrom. A second barb portion and stress-dispersing portion, may also extend from the basal portion.
Type:
Grant
Filed:
May 8, 2003
Date of Patent:
July 25, 2006
Assignee:
Cook Incorporated
Inventors:
William A. Cook, Michael P. DeBruyne, Benjamin Nickless, Thomas A. Osborne
Abstract: Method and apparatus implementing and using techniques for controlling flow in a body lumen, including use of an implantable medical device. The device includes a membrane implantable in a body lumen and invertibly deformable between a first position and a second position. The membrane is invertible in response to the direction of fluid flow through the lumen and can be deformable by fluid flow in the body lumen.
Abstract: Pannus-resisting implantable medical devices comprise one or more antimicrobial reservoirs, each such reservoir incorporating antimicrobial substances in predetermined distributions for timed release in vivo. Predetermined distributions of antimicrobial substances incorporated in antimicrobial reservoirs are achieved through use of fluid solvent carriers, which may comprise supercritical fluid solvents. Precipitation of antimicrobial substances from such solvent carriers in predetermined distributions is accomplished through evaporation and/or application of heating, cooling or decreased ambient pressure to the solvent carriers.
Type:
Grant
Filed:
December 21, 2000
Date of Patent:
July 25, 2006
Assignee:
Carbomedics Inc.
Inventors:
Joseph Andrew Chinn, R. Michael Casanova
Abstract: Devices and methods for treating heart valves include members that assist the valve in closing during at least a portion of the cardiac cycle. Such devices include members configured to alter the shape of a valve annulus, reposition at least one papillary muscle, and/or plug an orifice of the valve so as to provide a coaptation surface for the valve leaflets.
Type:
Grant
Filed:
June 15, 2004
Date of Patent:
July 18, 2006
Assignee:
Myocor, Inc.
Inventors:
Robert M. Vidlund, Jason E. Kalgreen, Todd J. Mortier, Cyril J. Schweich, Jr., Richard Schroeder, David Kusz
Abstract: The present invention provides improved stents and other prostheses for delivering substances to vascular and other luminal and intracorporeal enviroments. In particular, the present invention provides luminal prostheses which allow for a programmed and controlled substance delivery protocols for a variety of purposes. The prostheses comprise a scaffold which is implantable within a body lumen and a substance reservoir present over at least a portion of the scaffold. Usually, a rate-controlling element will be formed over the substance-containing reservoir to provide for a number of different substance release characteristics.
Abstract: An attachment system secures a residual limb to an artificial limb in a comfortable and substantially non-rotational manner. The attachment system offers proximal anchoring of the residual limb in a hard socket, by connecting a side surface of a residual limb liner to the side surface of the socket. Preferably, this connection is accomplished using an extension member extending from the liner through a portion of the socket interior, through the socket wall, and attaching to a latch mechanism. The preferred attachment system requires no clearance in the bottom of the socket well because neither the extension member nor the latch mechanism is located between the distal end of the residual limb/liner and the bottom of the well. The attachment system is preferably disposed entirely along the side of the limb and the side of the socket.
Abstract: A first stent delivery system provided with a sheath for covering the stent, the sheath including proximal sheath portion adapted to be movable in a proximal direction and a distal sheath portion adapted to be moveable in a distal direction. A second stent delivery system including an outer and intermediate tubular members covering a chamber with a preloaded stent, the outer tubular member being retractable prior to the retraction of the intermediate sheath and release of the stent. A third stent delivery system including with an inflatable balloon at a distal end of the system for fixing the system in place within the vessel prior to the release of the stent thereby insure accurate stent deployment.
Abstract: An appliance 10 for large saphenous vein varix treatment comprises a stainless steel guide wire 1 provided on a distal end with a guide portion 11 and on a proximal end with a coupled portion 12, an absorption thread 2 connected to the proximal end coupled portion 12 of the guide wire 1, a transparent flexible bag 3 for containing the absorption thread 2, and a sterilization holding case 4 for containing the guide wire 1 and the transparent flexible bag 3 in a sterilized condition. Upon use, the sterilization holding case 4 is opened, a vein sclerosing agent is injected into the transparent flexible bag 3, and the vein sclerosing agent is impregnated into the absorption thread 2.