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FDA 510(k) Applications Submitted by MICHELLE GODIN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K170086
01/10/2017
Pinnacle Radiation Therapy Planning System
Philips Medical Systems (Cleveland), Inc.
K100229
01/26/2010
VENTRIO HERNIA PATCH
C.R. BARD, INC.
K101851
07/01/2010
VENTRALIGHT ST MESH
DAVOL INC., SUB. C.R. BARD, INC.
K101920
07/09/2010
VENTRIO ST HERNIA PATCH
C.R. BARD, INC.
K101928
07/09/2010
VENTRALEX ST HERNIA PATCH
C.R. BARD, INC.
K143111
10/29/2014
Codman Certas Plus Programmable Valve; Codman Certas Toll Kit
MEDOS INTERNATIONAL SARL
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