The objective of this study is to assess the safety and feasbility of an investigational microwave ablation probe and generatory delivered using a robotic-assisted bronchoscopy system for the transbronchial ablation of pulmonary tumors. Enrolled subjects are those indicated for non-surgical intervention of confirmed lung cancer. Subjects will be followed through 24 months post-procedure, assessing procedure success as well as outcomes such as local recurrnence and progression free survival. Quality of life measures using validated tools will also be collected.
