Aurora Spine's ZIP Fusion System Receives FDA 510(k) Clearance

Spinal Tech

Aurora Spine has been granted FDA 510(k) clearance for its ZIP minimally invasive interspinous fusion system. The ZIP system was designed to be a pedicle screw alternative. It has already launched in Europe and will immediately launch in the U.S. with its new approval. Aurora Spine has 35 U.S. distributors for ZIP sales.

More Articles on Spine:

Device Companies — 7 Key Notes — Smith & Nephew, NuVasive & More
NuVasive to Exhibit, Participate in German Spine Society Annual Meeting
NLT Spine Awarded Two US Patents for PROW Interbody Fusion Procedure

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

 

Featured Webinars

Featured Whitepapers