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.
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


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