FDA 510(k) Applications Submitted by STEPHEN BEIER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K230960	04/05/2023	DLPÖ Silicone Coronary Artery Ostial Cannulae	Medtronic, Inc.
K251258	04/23/2025	MC2Ö Two-Stage Venous Cannula; MC2XÖ Three-Stage Venous Cannula	Medtronic, Inc
K231206	04/27/2023	DLP Silicone Coronary Artery Ostial Cannulae	Medtronic, Inc.
K093163	10/06/2009	INTEGRA TOTAL WRIST FUSION SYSTEM	INTEGRA LIFESCIENCES CORPORATION
K093781	12/09/2009	MODIFIED: NEWDEAL HALLU PLATES	NEWDEAL SAS
K093914	12/22/2009	NEWDEAL COMPRESSION PLATES	NEWDEAL SAS
K130557	03/04/2013	NEURAGEN 3D	INTEGRA LIFESCIENCES CORPORATION
K123000	09/27/2012	INTEGRA TOTAL FOOT SYSTEMS	INTEGRA LIFESCIENCES CORPORATION
K113104	10/20/2011	INTEGRA WOUND MATRIX (THIN)	INTEGRA LIFESCIENCES CORPORATION