A Formal Report Exploring the Addition of Endoscopic Suturing as an Anti-Migration Feature for Boston Scientific's VICI Venous Stent System

dc.contributor.authorEdwards, Nicholas
dc.date.accessioned2025-06-03T16:00:26Z
dc.date.available2025-06-03T16:00:26Z
dc.date.published2024
dc.descriptionKirmser Undergraduate Research Award - Individual Non-Freshman category, grand prize
dc.description.abstractSubmitted to the Senior Vice and President and President of Boston Scientific's Interventional Cardiology Therapies division, this report explores the product failure of the VICI VENOUS STENT System from the perspective of a device development engineer. Key sections include reasons for design failure, the benefits and drawbacks associated with a product recall, as well as identified solutions through a new R&D interdisciplinary team to support Boston Scientific's mission in transforming lives through innovative solutions. Through countless submission in English 415, this Formal Report showcases the final exploration into the FDA's Device Development Process, which I will be directly entering in my new role after Graduation.
dc.description.advisorPhillip Marzluf
dc.description.courseEnglish 415: Written Communication for Engineers
dc.identifier.bibliographicCitationEdwards, N. (2024). A formal report exploring the addition of endoscopic suturing as an anti-migration feature for Boston Scientific's VICI Venous Stent System. Unpublished manuscript, Kansas State University, Manhattan, KS.
dc.identifier.urihttps://hdl.handle.net/2097/45107
dc.publisherKansas State University. Dept. of English.
dc.subjectVICI Venous Stent System
dc.subjectBoston Scientific
dc.subjectFood and Drug Administration Device Development Process
dc.subjectInnovative Healthcare Transformation
dc.subjectDevice Development Engineering
dc.titleA Formal Report Exploring the Addition of Endoscopic Suturing as an Anti-Migration Feature for Boston Scientific's VICI Venous Stent System
dc.typeText

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