Cagent Vascular Announces FDA 510(k) Clearance for its Serranator Device for the Infrapopliteal Indication and Completion of its PRELUDE-BTK Clinical Trial Enrollment
https://cagentvascular.com/news/serranator-device
Cagent Vascular Initiates Enrollment of PRELUDE-BTK Study Using Serranator Device
https://cagentvascular.com/news/prelude-btk
Cagent Vascular Appoints Medical Device Industry Veteran Brian Walsh as Chairman of the Board
Cagent Vascular raises $11.87M to fund the growth and expansion of the SERRANATOR family of Percutaneous Transluminal Angioplasty (PTA) Serration Balloon Catheters