FDA 510(k) Applications Submitted by DIANA SMITH
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K040130 |
01/21/2004 |
ANTERIOR LUMBAR BUTTRESS SYSTEM |
SEASPINE |
K090161 |
01/22/2009 |
EPIPHANY INJECTION SYSTEM |
STAAR SURGICAL CO. |
K011028 |
04/05/2001 |
SCREW-VENT DENTAL IMPLANT SYSTEM |
SULZER DENTAL, INC. |
K011038 |
04/05/2001 |
TAPER-LOCK DENTAL IMPLANT SYSTEM |
SULZER DENTAL, INC. |
K061342 |
04/15/2006 |
MALIBU SPINAL SYSTEM |
SEASPINE, INC. |
K031381 |
05/01/2003 |
UCR SPINAL SYSTEM, LAMINAR HOOKS, PEDICLE HOOKS, AND INSTRUMENTS |
SEASPINE |
K051663 |
06/22/2005 |
MALIBU SPINAL SYSTEM |
SEASPINE, INC. |
K051942 |
07/15/2005 |
MALIBU SPINAL SYSTEM |
SEASPINE, INC. |
K032368 |
08/01/2003 |
SONOMA ANTERIOR CERVICAL PLATE SYSTEM |
SEASPINE |
K052170 |
08/09/2005 |
SEASPINE VBR SYSTEM |
SEASPINE, INC. |
K032739 |
09/04/2003 |
UCR SPINAL SYSTEM |
SEASPINE |
K062934 |
09/28/2006 |
SIERRA |
SEASPINE, INC. |
K043232 |
11/22/2004 |
UCR SPINAL SYSTEM |
SEASPINE |
K073586 |
12/20/2007 |
MICROSTAAR INDIGO INJECTOR FOAM TIP SYSTEM |
STAAR SURGICAL CO. |
K073591 |
12/20/2007 |
MICROSTAAR MSI INJECTOR FOAM TIP SYSTEM |
STAAR SURGICAL CO. |
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