Medtronic Holding Company Sarl

Kyphon Sarl

Warsaw Orthopedic, Inc.

Medtronic Europe Sàrl

Calin Druma

Bruce Chabansky

Michael A Smith

Neil S Sasaki

Amy L Arthur

Travis J Nolan

Shankar Kar

Craig Edward Lauchner

Samuel V Bolosan

Hester Chan

Asha Sharma

Travis Nolan

Samuel Bolosan

A cooled radio-frequency (RF) ablation probe is provided. The RF ablation probe includes a first tubular portion defining at least part of an internal cavity for circulating coolant through the cooled RF ablation probe; a second tubular portion surrounding the first tubular portion along a first portion of the length of the cooled RF ablation probe; a third tubular portion surrounding the second tubular portion along a second portion of the length of the cooled RF ablation probe; and a fourth tubular portion surrounding the third tubular portion along a third portion of the length of the cooled RF ablation probe. A gap is defined between the third tubular portion and the fourth tubular portion that can be filled with air or a vacuum can be formed in the gap to insulate one or more thermocouples attached to the fourth tubular portion from the coolant in the internal cavity.

Cooled bipolar radio-frequency ablation probe

A surgical access system includes a cannula, a mapping spacer, and a trocar. The cannula includes a proximal base and an elongated cannula body extending distally therefrom. The mapping spacer is configured to releasably engage the proximal base and includes first and second uprights defining a slot therebetween. The trocar includes a proximal handle and an elongated trocar body extending distally therefrom to a distal cutting tip. The elongated trocar body is insertable through the mapping spacer and cannula. In a first orientation of the trocar relative to the mapping spacer, the proximal handle is configured to abut the first and second uprights to inhibit extension of the distal cutting tip from the proximal base beyond an initial position. In a second orientation of the trocar, the proximal handle is slidable through the slot to enable extension of the distal cutting tip distally towards an extended position.

Devices, systems, and methods facilitating access to and mapping of target tissue

An inflatable bone tamp for performing a minimally invasive surgical procedure includes an outer shaft defining an internal lumen, an inflatable structure coupled to the outer shaft, and an inner shaft movably disposed within the internal lumen and coupled to a distal end region of the inflatable structure. The internal lumen is sized to receive the inflatable structure, such that by moving the inner shaft relative to the outer shaft, the inflatable structure can be retracted into the internal lumen (and likewise can be extended from within the internal lumen for deployment in bone). This retraction capability can beneficially protect the inflatable structure during positioning/removal, and can also enhance recovery from radial tears of the inflatable structure.

Retractable inflatable bone tamp

A system for use in tumor ablation. The tumor ablation system includes a microwave antenna which has a channel along the length thereof. There are two ports proximate the proximal end of the microwave antenna. The first port is an energy port configured to connect the antenna to an energy source. The second port is a fluid port configured to connect the channel to a fluid delivery mechanism. The system also includes an inflatable balloon configured to be attached to a distal end of the antenna. The channel permits fluid access from the fluid port to an interior of the balloon for inflation thereof.

Tumor ablation system

An inflatable bone tamp including a first balloon portion and a second balloon portion is provided. Each of the first balloon portion and the second balloon portion include interior cavities that can be filled with liquid, and these interior cavities communicate with one another via a valve. The valve can limit or restrict flow of the liquid between the cavities. As such, the first balloon portion and the second balloon portion can be sequentially inflated with the liquid through use of the valve.

Inflatable bone tamp and method for use of inflatable bone tamp

A adaptor is used with a driver, a drill, and a cannula to facilitate removal of material from bone and placement of the cannula in the bone. The adaptor includes an end portion provided at a proximal first end that is configured to engage a portion of the drill; a body portion attached to the end portion and extending from the end portion toward a distal second end; a head portion provided at the distal second end and attached to the body portion; and a passageway for receiving the drill that extends through the adaptor. Furthermore, the head portion includes a distal surface and at least one coupler provided on or adjacent the distal surface for releasably engaging. the cannula.

Adaptor and drill for use with a driver and a cannula for drilling into bone

A kyphoplasty cannula includes a shaft extending between opposite first and second end surfaces. The shaft has an inner surface defining a lumen. The shaft has a first opening that extends through the first end surface and a second opening that extends through the second end surface. A scoop extends from the second end surface. The scoop has an arcuate inner surface that is continuous with the inner surface of the shaft an opposite outer surface. The scoop has a rib. Kits and methods of use are disclosed.

Vertebral body access cannula with enhanced bending stiffness

An inflatable bone tamp is provided that includes a shaft with proximal and distal portions and a central longitudinal axis. A balloon is attached to the shaft such that a material can flow through the shaft and into the balloon to inflate the balloon. A flow controller controls the flow of the material through the shaft and into the balloon. Kits, systems and methods are disclosed.

Inflatable bone tamp with flow control and methods of use

A adaptor is used with a driver, a drill, and a cannula to facilitate removal of material from bone and placement of the cannula in the bone. The adaptor includes an end portion provided at a proximal first end that is configured to engage a portion of the drill; a body portion attached to the end portion and extending from the end portion toward a distal second end; a head portion provided at the distal second end and attached to the body portion; and a passageway for receiving the drill that extends through the adaptor. Furthermore, the head portion includes a distal surface and at least one coupler provided on or adjacent the distal surface for releasably engaging, the cannula.

Adaptor for use with a driver, a drill, and a cannula for drilling into bone

An inflatable bone tamp for performing a minimally invasive surgical procedure includes a shaft having a primary region and a reduced diameter region, and an inflatable structure surrounding at least a portion of the reduced diameter region. The reduced diameter region of the shaft allows the deflated size of the inflatable structure to be minimized, while at the same time eliminating the need for the conventional dual lumen balloon catheter construction.

Low cost low profile inflatable bone tamp

An inflatable bone tamp is provided that includes a shaft defining a lumen. A balloon is coupled to the shaft such that a material can flow through the lumen and into the balloon to inflate the balloon. A connector is coupled to the shaft. The connector includes a first port and a second port. The ports are in communication with the lumen. A flow control device is coupled to the first port. The flow control device controls flow of the material through the first port and into the lumen. A damper is coupled to the second port. The damper controls pressure within the inflatable bone tamp when pressure within the inflatable bone tamp reaches a threshold. Kits, systems and methods are disclosed.

A surgical system including an expandable device is provided, including an inflatable body, an inner shaft and an outer shaft. The inflatable body has at least one folded segment, which are housed in a distal portion of the outer shaft. The inflatable body is tethered to a portion of the outer shaft. The inner shaft is affixed to a portion of the inflatable body, and is configured to control an axial and/or a radial inflation pattern of the folded inflatable body.

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San Jose, CA, United States of America

Calin Druma