FDA 510(k) Applications Submitted by MARY A FADERAN
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K070738 |
03/16/2007 |
SIS FACIAL CYLINDER, SIS FACIAL IMPLANT |
COOK BIOTECH, INC. |
K090688 |
03/16/2009 |
COOK UROLOGICAL GRAFT |
COOK BIOTECH, INC. |
K131015 |
04/11/2013 |
BIODESIGN ONLAY DURAL GRAFT OR BIODESIGN DURAPLASTY GRAFT |
COOK BIOTECH, INC. |
K062320 |
08/09/2006 |
SURGISIS PEYRONIE'S REPAIR GRAFT, MODEL SPR-100 |
COOK BIOTECH, INC. |
K132660 |
08/26/2013 |
NERVE CUFF |
COOK BIOTECH INCORPORATED |
K062696 |
09/11/2006 |
SURGISIS, SURGISIS ES |
COOK BIOTECH, INC. |
K062697 |
09/11/2006 |
SIS HERNIA REPAIR DEVICE, SURGISIS GOLD HERNIA REPAIR GRAFT |
COOK BIOTECH, INC. |
K073391 |
12/03/2007 |
SURGISIS BIODESIGN TISSUE GRAFT |
COOK BIOTECH, INC. |
K133011 |
09/25/2013 |
DIAPHRAGMATIC HERNIA GRAFT |
COOK BIOTECH, INC. |
K121360 |
05/07/2012 |
BIODESIGN ENT REPAIR GRAFT |
COOK BIOTECH INCORPRATED |
K111695 |
06/16/2011 |
HYBRID GRAFT |
COOK BIOTECH, INC. |
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