Medtronic Signia SDR Product Surveillance Registry
NCT05095935 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 430
Last updated 2026-01-07
Summary
The purpose of the registry is to confirm the safety and performance of the Signia™ Small Diameter Reload (SDR) when used in surgical procedures in a real-world setting in patients receiving surgery for indicated thoracic, abdominal, and pediatric applications, intraoperatively.
Conditions
- Minimally Invasive Surgical Procedures
- Surgical Procedures, Operative
Interventions
- OTHER
-
N/A observational registry
N/A observational registry
Sponsors & Collaborators
- lead INDUSTRY
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-08-10
- Primary Completion
- 2024-10-01
- Completion
- 2024-10-01
- FDA Device
- Yes
Countries
- United States
Study Locations
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