Non-emergent, Abdominal or Thoracic Procedures Clinical Trial
Official title:
A Post-market Study of the Endo GIA™ Reinforced Reload With Tri-Staple™ Technology
A post-market study of the Endo GIA™ Reinforced Reload with Tri-Staple™ Technology.
The objective of this prospective, two-arm, multicenter, post-market study is to evaluate safety through the incidence of reported device-related adverse events (AEs) through 30 days following use of the Endo GIA™ Reinforced Reload with Tri-Staple™ Technology in subjects undergoing indicated abdominal or thoracic procedures. ;
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment