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.
K250920	03/27/2025	Arthrex Spine Compression FT Screw	Arthrex, Inc.
K231113	04/19/2023	Arthrex FiberTak Suture Anchor	Arthrex Inc.
K241235	05/02/2024	Arthrex TightRope II	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.
K232742	09/07/2023	Arthrex FiberTak Suture Anchor	Arthrex Inc.
K232973	09/21/2023	Arthrex Knee FiberTak« Button Suture Anchor	Arthrex Inc
K113252	11/03/2011	PEEK PREVAIL CERVICAL INTERBODY DEVICE	MEDTRONIC SOFAMOR DANEK