FDA 510(k) Applications Submitted by MARK BLEYER
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K050246 |
02/02/2005 |
SIS DERMAL AUGMENTATION STRAND |
COOK BIOTECH, INC. |
| K050337 |
02/10/2005 |
SIS FISTULA PLUG |
COOK BIOTECH, INC. |
| K020654 |
02/28/2002 |
STRATASIS SLING KIT |
COOK BIOTECH, INC. |
| K020732 |
03/06/2002 |
SS MATRIX |
COOK BIOTECH, INC. |
| K010952 |
03/30/2001 |
SURGISIS GUIDED TISSUE REGENERATION MATRIX |
COOK BIOTECH, INC. |
| K031069 |
04/04/2003 |
SURGISIS NERVE CUFF |
COOK BIOTECH, INC. |
| K051048 |
04/25/2005 |
SURGISIS STAPLE LINE REINFORCEMENT II |
COOK BIOTECH, INC. |
| K031850 |
06/16/2003 |
DURASIS DURAL SUBSTITUTE |
COOK BIOTECH, INC. |
| K022044 |
06/24/2002 |
SURGISIS STAPLE LINE REINFORCEMENT |
COOK BIOTECH, INC. |
| K034039 |
12/29/2003 |
SIS PLASTIC SURGERY MATRIX |
COOK BIOTECH, INC. |
|
|
