Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fixation Device With Deep Purchase Tacks
NCT03526341 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 116
Last updated 2019-10-09
Summary
A post-market clinical follow-up study for ReliaTack™ articulating reloadable fixation device with deep purchase tacks
Conditions
- Inguinal Hernia
- Ventral Hernia
Interventions
- DEVICE
-
ReliaTack™ Articulating Reloadable Fixation Device
ReliaTack™ Articulating Reloadable Fixation Device with Deep Purchase Tacks
Sponsors & Collaborators
-
Medtronic - MITG
lead INDUSTRY
Principal Investigators
-
John W Odom, MD · St. Josephs/ Candler
-
Har Chi Lau, MD · Hudson Valley Surgical Group
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-04-25
- Primary Completion
- 2019-09-10
- Completion
- 2019-09-10
- FDA Device
- Yes
Countries
- United States
Study Locations
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