St. Jude Medical International Holding S.a.r.l.

Tsi, Inc.

Advance Research System, LLC

St. Jude Medical Luxembourg Holding S.a.r.l.

Advanced Research Systems, Inc.

Stuart J Olstad

Hamid R Abbasi

Giovanni Leo

Nicolas Aeby

Hendrik Lambert

Axel Bertholds

Pere Llosas

Kenneth R Barra

Olivier B Fremont

Richard Remiarz

Max Carideo

Ricky L Holm

Hai Zhang

Will Zanto

Qian Shi

Greg Olson

Phillip Poeschl

Vincent Majkowski

Oliver B FRÉMONT

A handheld microscope for direct, optical viewing of surgical sites. The system includes an illumination system, as well as viewing optics contained in a housing, the housing being configured for coupling to a proximal end of an access port. In some embodiments, the access port houses a light probe coupled to a source of the illumination system for irradiation of the surgical area. The system may include aspiration capability for clearing debris from the surgical site.

Handheld microscope for cannulated surgical systems

An ablation catheter system configured with a compact force sensor at a distal end for detection of contact forces exerted on an end effector. The force sensor includes fiber optics operatively coupled with reflecting members on a structural member. In one embodiment, the optical fibers and reflecting members cooperate with the deformable structure to provide a variable gap interferometer for sensing deformation of the structural member due to contact force. In another embodiment, a change in the intensity of the reflected light is detected to measure the deformation. The measured deformations are then used to compute a contact force vector. In some embodiments, the force sensor is configured to passively compensate for temperature changes that otherwise lead to erroneous force indications. In other embodiments, the system actively compensates for errant force indications caused by temperature changes by measuring certain local temperatures of the structural member.

Compact force sensor for catheters

An endplate plunger for implanting a growth-promoting tether between opposed adjacent vertebrae. The endplate plunger includes resilient arm assemblies that store potential energy when the endplate plunger is in a retracted configuration. In transitioning from the retracted configuration to a deployed configuration, the potential energy is released in a burst of kinetic energy, causing tip portions at the distal ends of the resilient arm assemblies to be thrust into the adjacent vertebrae. In some embodiments, each tip portion forms a cleft in the respective vertebral endplate and deposits the tether therein. The tether is thereby anchored directly in the clefts, without need for separately formed anchors. In some embodiments, devices and methods are disclosed to route the tether through an implanted spinal implant.

Cannulated endplate plunger

A cannulated plunger assembly for setting a tether with anchors on both ends to extend between adjacent vertebrae. The cannulated form enables minimally invasive access to an evacuated space between the vertebral endplates. Each of the anchors are coupled to a respective one of a pair of plunger arms, the plunger arms being configured to deploy the anchors beyond an outer radius of a tubular housing. In some embodiments, in a retracted configuration, the pair of plunger arms are surrounded by the housing, and in a deployed configuration, the pair of plunger arms extend through an open distal end of and beyond an outer radius of the housing to drive the anchors into the vertebral end plates.

Cannulated endplate plunger assembly

A method and device for determining the transmurality and/or continuity of an isolation line formed by a plurality of point contact ablations. In one embodiment, a method for determining the size of a lesion (width, depth and/or volume) is disclosed, based on contact force of the ablation head with the target tissue, and an energization parameter that quantifies the energy delivered to the target tissue during the duration time of the lesion formation. In another embodiment, the sequential nature (sequence in time and space) of the ablation line formation is tracked and quantified in a quantity herein referred to as the 'jump index,' and used in conjunction with the lesion size information to determine the probability of a gap later forming in the isolation line.

Prediction of atrial wall electrical reconnection based on contact force measured during RF ablation

A method and device for determining the transmuriality and/or continuity of an isolation line formed by a plurality of point contact ablations. In one embodiment, a method for determining the size of a lesion (width, depth and/or volume) is disclosed, based on contact force of the ablation head with the target tissue, and an energization parameter that quantifies the energy delivered to the target tissue during the duration time of the lesion formation. In another embodiment, the sequential nature (sequence in time and space) of the ablation line formation is tracked and quantified in a quantity herein referred to as the 'jump index,' and used in conjunction with the lesion size information to determine the probability of a gap later forming in the isolation line.

A head form for testing a variety of respirators. The head form can prevent false leak failures by having a mask registration member upon which the mask under test is mounted, the mask registration member being self lubricating. In one embodiment, the registration member is an inflatable bladder. The bladder can be configured to limit lift away of the inflatable bladder from the recess, thereby mitigating leaks in the head form assembly. The bladder may be configured to limit roll away of portions of the bladder that register against the head form, thereby reducing or eliminating leaks between the inflatable bladder and the mask under test.

Respirator test accessory

A hand-held, automated qualitative fit tester (QLFT) for establishing gas mask fit integrity. The automated QLFT may be configured to utilize a pressure source in combination with a cartridge and a nebulizer to generate aerosols having size distributions and concentrations that are substantially the same as OSHA-approved manual units. The QLFT may further include a cartridge that contains the aerosol solution used to test mask integrity. The cartridge may be configured to recapture solution that collects on the interior walls of the nebulizer. The automated QLFT may also be equipped with a microprocessor for executing sequences that are in substantive compliance with 29 CFR 1910.134 and for writing to a data storage device. The automated aspects of the invention can reduce or negate the need for operating personnel to repeatedly and manually actuate a squeeze ball and record results manually, as is required with present OSHA-approved hand-held aerosol generators.

Growing community of inventors

Plymouth, MN, United States of America

Stuart J Olstad