Cordis Receives FDA Clearance for Vascular Stent Systems for Use in SFA

Cordis Corp. has announced it has received FDA clearance for its S.M.A.R.T. CONTROL vascular stent systems for use in the superficial femoral artery and/or the proximal popliteal artery, according to a news release.

 

Cordis, part of the Johnson & Johnson family of companies, said the S.M.A.R.T. stent is the first stent in the Unites States with both iliac and SFA indications.

 

"We are very pleased to offer an expanded indication for the S.M.A.R.T. stent," said Shlomi Nachman, worldwide president of Cordis, in the release. "Our goal is to continue to make expanded indications and new products available to our customers so they may bring these innovations to their patients."

 

Related Articles on FDA Clearances:

LDR Receives FDA Conditional Approval for Cervical Disc

Intersect ENT Receives FDA Approval of Steroid-Releasing Implant

CareFusion Receives FDA Clearance for Take-Apart Laparoscopic Scissors

Copyright © 2024 Becker's Healthcare. All Rights Reserved. Privacy Policy. Cookie Policy. Linking and Reprinting Policy.

 

Featured Webinars

Featured Whitepapers