FDA 510(k) Applications Submitted by Nanovis Spine LLC

FDA 510(k) Number Submission Date Device Name Applicant
K162250 08/10/2016 FortiBridge Anterior Cervical Plate System NANOVIS SPINE LLC
K193211 11/21/2019 Nano FortiFix« System Nanovis Spine LLC
K143706 12/29/2014 FortiBridge Anterior Cervical Plate System Nanovis Spine LLC


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