FDA 510(k) Applications Submitted by STEPHANIE BAKER
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K081010 |
04/09/2008 |
BARD 3DMAX MESH |
DAVOL INC., SUB. C.R. BARD, INC. |
K081777 |
06/23/2008 |
VENTRIO HERNIA PATCH |
C.R. BARD, INC. |
K082396 |
08/19/2008 |
DAVOL ABSORBABLE FASTENER SYSTEM, MODEL (S) 0113080,0113081, 0113082, 0113084, 0113086, 0113087 |
C.R. BARD, INC. |
K063178 |
10/19/2006 |
BARD COLLAMEND IMPLANT, MODELS 1175102, 1175103, 1175104, 1175105, 1175106 |
C.R. BARD, INC. |
K113229 |
11/02/2011 |
VENTRIO LIGHT HERNIA PATCH WITH TRM ANTIMICROBIAL COATING |
C.R. BARD, INC. |
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