URL09/12/2022FDA Communications FDA Advisory Panel Recommendations on Lifelong Surveillance and Long-Term Postmarket Data Collection for Patients with AAA Endovascular Aortic Repair – Letter to Health Care Providers
URL03/09/2022FDA Communications Medtronic Recalls TurboHawk Plus Directional Atherectomy System Due to Risk of Tip Damage During Use
URL03/01/2022FDA Communications FDA Advisory Panel Recommendations on Lifelong Surveillance and Long-Term Postmarket Data Collection for Patients with AAA Endovascular Aortic Repair – Letter to Health Care Providers
URL01/24/2022FDA Communications The FDA has issued a Class 1 Device Recall for HawkOne – Please see the FDA’s Notice for Further Notification
URL01/13/2022FDA Communications FDA has issued an important Safety Communication Update on the Endologix AFX
