FDA 510(k) Applications Submitted by Kristi Frisch

FDA 510(k) Number Submission Date Device Name Applicant
K130640 03/11/2013 ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM MEDTRONIC SOFAMOR DANEK USA, INC.
K231113 04/19/2023 Arthrex FiberTak Suture Anchor Arthrex Inc.
K141632 06/18/2014 ZEVO (TM) ANTERIOR CERVICAL PLATE SYSTEM MEDTRONIC SOFAMOR DANEK USA, INC.
K231857 06/23/2023 Arthrex TightRope II Arthrex Inc.
K113252 11/03/2011 PEEK PREVAIL CERVICAL INTERBODY DEVICE MEDTRONIC SOFAMOR DANEK


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