Abstract: At least one aspect is directed to a totally artificial heart, and at least another aspect is directed to a method of controlling blood flow in a patient. The totally artificial heart may include a first rotary pump having an input to receive blood and an output to provide blood to a patient's lungs, a second rotary pump having an input to receive blood and an output to provide blood to the patient's body, a first sensor associated with the first rotary pump, a second sensor associated with the second rotary pump, and a control system coupled to the first sensor, the second sensor, the first rotary pump and the second rotary pump and configured to control characteristics of the first rotary pump and the second rotary pump based on signals received from at least one of the first sensor and the second sensor such that an average flow of blood through the second rotary pump is greater than an average flow of blood through the first rotary pump.

Abstract: Spinal implants and methods for spinal stabilization and/or fusion are provided. Exemplary implants described herein can be configured for delivery to a facet joint to stabilize and/or fuse the facet joint, and can optionally be anchored within the pedicle for added fixation. The implant can optionally include a fusion-promoting bioactive material thereby providing a single device capable of spinal stabilization and/or fusion. Furthermore, a method of placing such an implant within a facet joint is provided.

Abstract: A rotary blood pump comprises a housing and a rotor. The housing includes a blood inlet, a blood outlet, a blood flow conduit disposed between the blood inlet and the blood outlet, and a rotary bearing assembly disposed within and fixed to the housing. The rotor is rotatably disposed within the housing and includes one or more impellor blades disposed within the blood flow conduit for pumping blood through the conduit, and a shaft affixed to and rotating with the rotor. The shaft rotatably engages the bearing assembly to define an intersection between the rotor and the housing and to provide relative rotation between the rotor and the housing. In addition, the shaft further defines an axis of rotation for the rotor. In the rotary pump of the invention, at least one of the rotor and the housing defines a swirl region proximate to the intersection between the rotor and the housing.

Abstract: The invention provides a transcutaneous energy transfer device having an external primary coil and an implanted secondary coil inductively coupled to the primary coil, electronic components subcutaneously mounted within the secondary coil and a mechanism which reduces inductive heating of such components by the magnetic field of the secondary coil. For one embodiment of the invention, the mechanism for reducing inductive heating includes a cage formed of a high magnetic permeability material in which the electronic components are mounted, which cage guides the flux around the components to prevent heating thereof. For an alternative embodiment of the invention, a secondary coil has an outer winding and either a counter-wound inner winding or an inner winding in the magnetic field of the outer winding. For either arrangement of the inner coil, the inner coil generates a magnetic field substantially canceling the magnetic field of the outer coil in the area in which the electronic components are mounted.

Abstract: A substantially flexible primary coil for use in a transcutaneous energy transfer (TET) device. When in use, the primary coil conforms to the contours of a patient's body, and, more particularly, to the shape of the skin under which a secondary coil of the TET is implanted. The shape of the primary coil adjusts with short term and long term changes in the contour of the patient's skin, enabling the primary coil to maintain a desired relative position with the implanted secondary coil as the patient changes position, posture or orientation, as well as over time as the patient loses or gains weight. The primary coil includes a shape-retaining base ring defining a primary plane. The base ring is firm, yet is able to conform to the contours of the substrate upon which it is placed. Attached to the base ring is a conducting element such as flexible wire which is coiled to form a plurality of nearly concentric windings.

Abstract: The invention provides a transcutaneous energy transfer device having an external primary coil and an implanted secondary coil inductively coupled to the primary coil, electronic components subcutaneously mounted within the secondary coil and a mechanism which reduces inductive heating of such components by the magnetic field of the secondary coil. For one embodiment of the invention, the mechanism for reducing inductive heating includes a cage formed of a high magnetic permeability material in which the electronic components are mounted, which cage guides the flux around the components to prevent heating thereof. For an alternative embodiment of the invention, a secondary coil has an outer winding and either a counter-wound inner winding or an inner winding in the magnetic field of the outer winding. For either arrangement of the inner coil, the inner coil generates a magnetic field substantially canceling the magnetic field of the outer coil in the area in which the electronic components are mounted.

Abstract: The invention provides a transcutaneous energy transfer device having an external primary coil and an implanted secondary coil inductively coupled to the primary coil, electronic components subcutaneously mounted within the secondary coil and a mechanism which reduces inductive heating of such components by the magnetic field of the secondary coil. For one embodiment of the invention, the mechanism for reducing inductive heating includes a cage formed of a high magnetic permeability material in which the electronic components are mounted, which cage guides the flux around the components to prevent heating thereof. For an alternative embodiment of the invention, a secondary coil has an outer winding and either a counter-wound inner winding or an inner winding in the magnetic field of the outer winding. For either arrangement of the inner coil, the inner coil generates a magnetic field substantially canceling the magnetic field of the outer coil in the area in which the electronic components are mounted.

Abstract: The invention provides a transcutaneous energy transfer device having an external primary coil and an implanted secondary coil inductively coupled to the primary coil, electronic components subcutaneously mounted within the secondary coil and a mechanism which reduces inductive heating of such components by the magnetic field of the secondary coil. For one embodiment of the invention, the mechanism for reducing inductive heating includes a cage formed of a high magnetic permeability material in which the electronic components are mounted, which cage guides the flux around the components to prevent heating thereof. For an alternative embodiment of the invention, a secondary coil has an outer winding and either a counter-wound inner winding or an inner winding in the magnetic field of the outer winding. For either arrangement of the inner coil, the inner coil generates a magnetic field substantially canceling the magnetic field of the outer coil in the area in which the electronic components are mounted.

Abstract: A transcutaneous energy transfer device is provided which has a magnetic shield covering the primary winding of the device to reduce sensitivity of the device to conducting objects in the vicinity of the coils and to increase the percentage of magnetic field generated by the primary coil which reaches the secondary coil. This shield is preferably larger than the primary coil in all dimensions and is either formed of a high permeability flexible material, for example a low loss magnetic material in a flexible polymer matrix, with perforations formed in the material sufficient to permit ventilation of the patient's skin situated under the shield, or the shield may be formed of segments of very high permeability material connected by a flexible, porous mesh material.

Abstract: A magnetically operated blood pump includes a rotor with an impeller that rotates within a housing, and the housing fastens to a driver that preferably electromagnetically controls the speed and disposition of the impeller in response to sensed conditions. The impeller and housing constitute a disposable assembly in which permanent magnets embedded in the impeller stabilize its position to maintain pumping tolerances in at least one dimension, and also couple to external fields to rotate the impeller. In one embodiment concentric arrangements of cylinder magnets passively maintain radial centering, while coils in the driver are actuated to simultaneously produce a rotational torque and to correct axial or tilt displacements. In a preferred embodiment of this type, sensors around the periphery detect axial displacement and/or tilt as the impeller turns, while the drive circuit responds to the sensor signal to produce compensating phase changes in the coil drive signals.

Abstract: The invention is a disk-shaped screen adapted for removable placement onto one end of a standard-type oil filter. When the screen is placed on the oil filter, it is located in an area bounded by the oil filter's mounting gasket and it overlies the filter's inlet ports. The screen is made of a wire mesh having approximately 1600 openings per square inch. The screen functions to collect larger-sized particles from the oil stream before they enter the interior of the oil filter. By collecting these particles in a readily viewable manner, the screen enables a person to easily determine from the types and size of collected particles if any unusual engine wear has occurred or if the engine has suffered internal damage.