FDA 510(k) Applications Submitted by LAURA D KREJCI
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K091470 |
05/18/2009 |
RANASYS EZ NEGATIVE PRESSURE WOUND THERAPY SYSTEM, MODEL 66800059 |
SMITH & NEPHEW, INC. |
| K031981 |
06/26/2003 |
2.4 SMARTNAIL, MODELS 532416, 532425, 532435, 532445 |
LINVATEC BIOMATERIALS, LTD. |
| K082211 |
08/06/2008 |
RENASYS-F NEGATIVE PRESSURE WOUND THERAPY FOAM DRESSING KITS |
Smith & Nephew, Inc |
| K082426 |
08/22/2008 |
RENASYS EZ |
SMITH & NEPHEW, INC. |
| K032607 |
08/25/2003 |
POWERPRO PNEUMATIC SYSTEM, MODELS PRO6150, PRO6175, PRO6185 |
LINVATEC CORP. |
| K083375 |
11/14/2008 |
RENASYS GO NEGATIVE PRESSURE WOUND THERAPY |
SMITH & NEPHEW, INC. |
| K031994 |
06/27/2003 |
LINVATEC 300W XENON LIGHT SOURCE |
LINVATEC CORP. |
| K033573 |
11/13/2003 |
LINVATEC 10K IRRIGATION SYSTEM |
LINVATEC CORP. |
| K033748 |
12/01/2003 |
TRIDENT RESECTION ABLATOR |
LINVATEC CORP. |
| K033804 |
12/08/2003 |
BIOANCHOR WITH DISPOSABLE DRIVER |
LINVATEC CORP. |
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