FDA 510(k) Applications Submitted by KATIE LOGEROT
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K030319 |
01/30/2003 |
ORTHOSPHERE CERAMIC SPHERICAL IMPLANT |
WRIGHT MEDICAL TECHNOLOGY, INC. |
K060630 |
03/09/2006 |
REFLECTION 3-HOLE SHELL WITH ASYMMETRIC POROUS COATING |
SMITH & NEPHEW, INC. |
K041114 |
04/28/2004 |
PROFEMUR TAPERED HIP STEM |
WRIGHT MEDICAL TECHNOLOGY, INC. |
K061253 |
05/04/2006 |
REFLECTION 3 ACETABULAR SYSTEM |
SMITH & NEPHEW, INC. |
K041425 |
05/28/2004 |
CONSERVE PLUS REVISION SHELL AND CONSERVE PLUS THICK SHELL |
WRIGHT MEDICAL TECHNOLOGY, INC. |
K031963 |
06/25/2003 |
CONSERVE PLUS SPIKED ACETABULAR SHELLS AND CONSERVE TOTAL 56MM FEMORAL HEAD |
WRIGHT MEDICAL TECHNOLOGY, INC. |
K033456 |
10/30/2003 |
EVOLVE RADIAL PLATE |
WRIGHT MEDICAL TECHNOLOGY, INC. |
K043059 |
11/05/2004 |
COMPRESSION STAPLE AND SIMPLE STAPLE |
WRIGHT MEDICAL TECHNOLOGY, INC. |
K033529 |
11/10/2003 |
TIE-IN TRAPEZIUM |
WRIGHT MEDICAL TECHNOLOGY, INC. |
K033890 |
12/16/2003 |
ADVANCE DOUBLE HIGH INSERT |
WRIGHT MEDICAL TECHNOLOGY, INC. |
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