FDA 510(k) Applications Submitted by Aurora Spine

FDA 510(k) Number Submission Date Device Name Applicant
K133091 09/30/2013 ZIP MIS INTERSPINOUS FUSION SYSTEM AURORA SPINE
K133967 12/24/2013 INTERBODY CAGE SYSTEM AURORA SPINE
K243865 12/17/2024 AERO MIS Facet Fusion System Aurora Spine


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact