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FDA 510(k) Applications Submitted by STEFAN WALTER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K100056
01/08/2010
MEDCOM RT-VIEWER SYSTEM
MEDCOM GMBH
K080742
03/17/2008
VERISUITE 1.6, VERISUITE-PARTICLE 1.6
MEDCOM GMBH
K102237
08/09/2010
PVS MODEL 1.0
MEDCOM GMBH
K032550
08/18/2003
EXOMIO, MODEL 2.0 SP1
MEDCOM GMBH
K092653
08/28/2009
VERISUITE AND VERISUITE-PARTICLE, VERSION 1.8
MEDCOM GMBH
K193352
12/04/2019
AbutmentCAD
exocad GmbH
K183458
12/13/2018
exoplan 2.3
exocad GmbH
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