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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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