Stryker
Senior Director, Marketing and Education
Stryker Jan 2008 - Mar 2012
Director of Marketing
Stryker Jan 2005 - Dec 2007
Sales Representative
Stryker Jun 2002 - Dec 2004
Marketing Manager
Stryker Jun 1998 - Jan 2002
Design Engineer
Education:
University of Idaho 1994 - 1998
Bachelor of Science In Mechanical Engineering, Bachelors, Mechanical Engineering
M. Todd Miller - Saratoga CA, US Ryan E. Yearsley - Palo Alto CA, US Lonnie E. Paulos - Salt Lake City UT, US
Assignee:
Stryker Endoscopy - San Jose CA
International Classification:
A61B 17/58 A61B 17/60 A61F 2/00
US Classification:
606 98
Abstract:
A system for securing a graft within a bone includes a tubular cross pin having an interior surface bounding a passageway extending between a proximal end and an opposing distal end, the distal end terminating at a distal end face. A guide pin has an exterior surface extending between a proximal end and an opposing distal end, the exterior surface including an outwardly projecting shoulder. The guide pin is removably received within the passageway of the cross pin such that the distal end face of the cross pin biases against the shoulder and a proximal portion of the guide pin freely projects beyond the proximal end of the cross pin.
M. Miller - Saratoga CA, US Ryan Yearsley - Palo Alto CA, US Lonnie Paulos - Salt Lake City UT, US
Assignee:
Stryker Endoscopy
International Classification:
A61B017/56
US Classification:
606/072000
Abstract:
A system for securing a graft within a bone includes a tubular cross pin having an interior surface bounding a passageway extending between a proximal end and an opposing distal end, the distal end terminating at a distal end face. A guide pin has an exterior surface extending between a proximal end and an opposing distal end, the exterior surface including an outwardly projecting shoulder. The guide pin is removably received within the passageway of the cross pin such that the distal end face of the cross pin biases against the shoulder and a proximal portion of the guide pin freely projects beyond the proximal end of the cross pin.
- Mahwah NJ, US Ryan E. Yearsley - Denver CO, US Kyle Craig Pilgeram - San Jose CA, US
International Classification:
A61B 17/04
Abstract:
In one embodiment of the present invention, a fixation device including a sleeve member including an interior and an exterior surface along a length defined between a first end and a second end, and at least two openings positioned along the length and extending from the interior and through the exterior surface; and a filament including a first free end and a second free end and a length therebetween, the filament positioned relative to the sleeve member such that the free ends extend from the sleeve member at the first and second ends of the sleeve member, the filament being disposed inside the interior from the first end to a first opening, outside the sleeve member from the first opening to a second opening, and inside the interior from the second opening to the second end of the sleeve member.
- Mahwah NJ, US Ryan E. Yearsley - Denver CO, US M. Todd Miller - Shrewsbury MA, US Chad Lewis - Layton UT, US Daniel F. Justin - Orlando FL, US Margaret Mary Sinnott - Logan UT, US
International Classification:
A61B 17/04 A61B 17/16
Abstract:
A system for implanting an anchor into bone, the system comprising a curved cannulated guide for percutaneous insertion, having a proximal end and a distal end; a flexible drill insertable through the curved guide from the proximal end to the distal end, the flexible drill having a shaft having a flexible portion; and a flexible inserter for inserting a suture anchor into a bore at the anatomical site formed by the flexible drill, the flexible inserter having a shaft having a flexible portion, wherein the flexible portions of both the flexible drill and flexible inserter include a series of discrete, interlocking segments.
- Mahwah NJ, US Ryan E. Yearsley - Denver CO, US Kyle Craig Pilgeram - San Jose CA, US
International Classification:
A61B 17/04
Abstract:
One embodiment of the present invention includes a filamentary fixation system including a sleeve formed of filamentary material including an interior and an exterior surface along a length defined between a first end and a second end, the sleeve having a coating adapted to allow for tissue ingrowth, and a filament formed of filamentary material including a first free end and a second free end, and a length therebetween, at least a portion of the filament positioned within the interior of the sleeve.
- Kalamazoo MI, US José Raúl Marchand - San Juan PR, US Ryan E. Yearsley - Denver CO, US Kyle Craig Pilgeram - San Jose CA, US
International Classification:
A61L 17/00 A61L 17/14 A61L 17/06 A61B 17/04
Abstract:
In one embodiment, the present invention is a method of preparing a bioactive filamentary fixation device in situ, including (a) providing a filamentary fixation device including a sleeve member and a filament; (b) providing a physiological solution; (c) providing bioactive material; (d) wetting the sleeve of the fixation device with the physiological solution to produce a wetted sleeve; and (e) applying the bioactive material to the wetted sleeve to coat the sleeve, thus producing a bioactive filamentary fixation device at the time of surgery in situ.