www.fdanews.com/articles/189464-contego-medical-cleared-for-angioplasty-system
Contego Medical Cleared for Angioplasty System
December 7, 2018
The FDA has granted 510(k) clearance for Contego Medical’s Vanguard IEP, a peripheral balloon angioplasty system designed to keep patients at high risk of embolization safe during angioplasties.
The device is designed to protect patients that are vulnerable to embolization — the passage and lodging of an object, such as a blood clot, in the blood stream — during peripheral angioplasties, in which a surgeon repairs or unblocks blood vessels.
The system, which has an over-the-wire design, is able to protect the patient’s lower limbs during angioplasty and requires no additional devices or exchanges.