Preclinical medical device testing: how do you know you are ready and how do you make the most efficient investment in preclinical?
Surefire Medical achieves FDA 510(k) clearance for direct-to-tumor embolization device Surefire Precision in just 76 days with the help of T3 Labs.
Nerve Response Post Renal Denervation: Preclinical Testing Generates First Of Its Kind Documentation
Characterizing nerve response post renal denervation is the most critical aspect of any preclinical renal denervation study. Nerve atrophy, healing changes (fibrosis), condition of the perineurium, neuromatous regeneration; all of these aspects determine the success or failure of the denervation treatment. We are honored to present our most recent publication: “Neuromatous Regeneration as a Nerve…