324 results about "Implant surgery" patented technology

Prosthetic mitral heart valves and anchors for use with such valves are provided that allow for an improved implantation procedure. In various embodiments, a helical anchoring device is formed as a coiled or twisted anchor that includes one or more turns that twist or curve around a central axis. Curved arms attached to the frame of the valve guide the helical anchoring device into position beneath the valve leaflets and around the mitral valve annulus as it exits the delivery catheter, and the expandable prosthetic mitral valve is held within the coil of the anchoring device. The anchoring device and the valve can be delivered together, simplifying the valve replacement procedure.

A prosthetic implant for replacing a facet joint of a spinal motion segment includes a generally conical superior component adapted to be implanted at a surgically prepared site on a lower articular process of a cephalad vertebra of a spinal motion segment, and a cup-shaped inferior component adapted to be implanted at a surgically prepared site on a superior articular process of a caudad vertebra of the spinal motion segment.

Surgical procedures, tools and implants are disclosed for both conventional and reverse shoulder implant surgeries. The improved procedures, tools and implants relate to humeral head resurfacing, humeral head resection for standard implants, humeral head resection for reverse shoulder implants, glenoid resurfacing for standard shoulder implants and glenoid resurfacing for reverse shoulder implants. 3D scans and x-rays are used to develop virtual models of the patient anatomy, identify patient specific landmarks for anchoring guide wire installation blocks, templates and drill guides. 3D scans are also used to design patient specific tools and implants for the shoulder implant procedures and to pre-operatively determine the appropriate inclination and retroversion angles.

A driver apparatus for implanting spinal rod fixation devices including an anchor member and a coupling member pivotable relative to the anchor member is disclosed. The driver apparatus generally immobilizes the anchor member and coupling member relative to each other and to the driver apparatus during insertion to minimize interference between the coupling member and tissues surrounding the implantation site, as well as to minimize the clearance required for implantation. The driver apparatus includes a driver portion engageable with the anchor member for effecting seating of the anchor member, such as by threadably driving the anchor member in the bone. The driver portion is closely fit between portions such as upstanding walls of the coupling member to prevent relative rotation therebetween. The driver apparatus further includes locking portions shiftable to secure the coupling member with the driver apparatus when the driver is engaged with the anchor member

A pin placement instrument for placing a pin in a bone comprises an anatomical interface with a hook-like portion being opened in a lateral direction of the instrument to receive a bone therein in a planned position. A drill guide is connected to the anatomical interface and defining at least one guide slot in a longitudinal direction of the instrument. The guide slot has a lateral opening over its full length in the drill guide to allow lateral withdrawal of the instrument in said lateral direction with the pin placed in the bone passing through the lateral opening. A bushing is removably placed in said guide slot via said longitudinal direction in a planned fit, the bushing defining a throughbore aligned with the guide slot and adapted to receive the pin extending in said longitudinal direction when the bushing is in the guide slot for pin placement.

Intravascular devices and methods are provided for forming a vascular graft by axially distending a blood vessel to induce growth. These devices advantageously can be implanted via a catheter, thereby eliminating the need for a more invasive implantation procedure when the stretching is to be done in vivo. Preferably, the device for axially distending a blood vessel to induce growth of the vessel includes an intravascular stretching mechanism attachable directly to an interior lumen portion of the blood vessel, and a means for operating the stretching mechanism to cause the vessel to distend axially. The stretching mechanism can include a pair of wires or stents that engage the blood vessel wall. Components of the stretching mechanism can include a shape memory material.

The invention relates to the fields of computer-aided technology and maxillofacial plastic medical apparatus and instruments, in particular to an optimal design and manufacturing method for a jaw defect individual restoration. The optimal design and manufacturing method is characterized by comprising the following steps: conducting CBCT scanning on the maxillofacial part of a patient, obtaining DICOM data, guiding the data into three-dimensional modeling software-MIMICS (Materialise, Belgium) to reconstruct a jaw three-dimensional model, designing the individual restoration, designing models of a plurality of virtual screw according to the size of retention screws supposed to be adopted, then moving the models to the appropriate positions of the jaw to simulate the situation to the screw retention restoration, obtaining Von Mises stress and a strain nephogram, and manufacturing entities of various materials through the fast forming technology. The jaw defect individual restoration made through the manufacturing method for the jaw defect individual restoration has good performance in biomechanical properties including breaking strength, stress-strain distribution, the service life and the like. So far, a patient with upper and lower jaw defects accepting an implanting operation is observed for two years, and no bad complications of fracture, exposure and the like happen.

The present invention provides a prosthetic tissue or sheet capable of withstanding implantation operations, which can be used in actual operation and can be produced by culture. The present invention also provides a novel therapy which can substitute for cell therapy. Particularly, the present invention provides a method for producing a prosthetic tissue comprising a cell derived from a part other than myocardium and capable of withstanding implantation operation. The above-described objects of the present invention were partially achieved by finding that by culturing cells under specific culture conditions, the cells are unexpectedly organized into a tissue, and the resultant prosthetic tissue is capable of being detached from culture dishes. The present invention also provides a three-dimensional structure applicable to heart, comprising a cell derived from a part other than the myocardium of an adult.

A method of making a surgical template comprises: producing a 3-D geometrical image by a CT scanning performed on a patient's jaw and establishing corresponding implant planning data to obtain a 3-D first digital image, making a positive plaster model of the patient's jaw, scanning the plaster model to obtain a 3-D second digital image, overlapping the second digital image on the first digital image to obtain a computer representation of the plaster model and at least one implant to be mounted according to the implant planning data, drilling the plaster model to form at least one pinhole according to the implant planning data, inserting a pin into the pinhole, producing a negative template body from an assembly of the plaster model and the pin with a thermoplastic dental material so that the negative template body has at least one implant guide hole and constitutes the surgical template.

An approach is disclosed that involves creating an updated master dental model of a patient's mouth after an implant surgery by aligning new postoperative oral scan data to pre-existing preoperative oral scan data that is more comprehensive (e.g., it includes bite registration). Before surgery a multi-piece stackable surgical guide set is created using the preoperative oral scan data. The surgical guide set is used to facilitate the surgery. After the surgery at least one piece of the surgical guide set is placed back in a patient's mouth and may act as a reference marker because it was created using the preoperative oral scan data, but is also part of the postoperative mouth configuration since it was used to facilitate the surgery. The affected portion of the mouth may then be digitally scanned directly or indirectly by way of a physical impression with the reference marker in place to determine the new characteristics resulting from the surgery such as new implant installation locations and orientations. The new postoperative oral scan data may be combined with the pre-existing preoperative oral scan data by way of the reference marker (since it is a constant between the two sets of scan data) without having to do such things as take a new bite registration, on which a new implant restoration can be easily created.