FDA 510(k) Applications Submitted by KINAMED, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K122049 |
07/12/2012 |
NEUROPRO LOW PROFILE CRANIAL PLATING SYSTEM |
KINAMED, INC. |
K003347 |
10/25/2000 |
ORTHOPILOT |
KINAMED, INC. |
K994214 |
12/14/1999 |
GEM KNEE SYSTEM |
KINAMED, INC. |
K982927 |
08/20/1998 |
QUICK TAP SELF DRILLING SCREW |
KINAMED, INC. |
K964362 |
11/01/1996 |
KINAMED PROFIX SYSTEM |
KINAMED, INC. |
K010101 |
01/11/2001 |
GEM POSTERIOR STABILIZED TOTAL KNEE SYSTEM |
KINAMED, INC. |
K030256 |
01/24/2003 |
ISO-ELASTIC CERCLAGE SYSTEM |
KINAMED, INC. |
K032950 |
09/22/2003 |
GEM INSET PATELLAR COMPONENT |
KINAMED, INC. |
K013982 |
12/03/2001 |
KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT |
KINAMED, INC. |
K020764 |
03/07/2002 |
NAVIPRO |
KINAMED, INC. |
K050897 |
04/08/2005 |
NAVIPRO SHOULDER SOFTWARE MODULE |
KINAMED, INC. |
K072250 |
08/13/2007 |
SUPERCABLE GRIP AND PLATE SYSTEM |
KINAMED, INC. |
K033668 |
11/21/2003 |
NAVIPRO KNEE SOFTWARE MODULE |
KINAMED, INC. |
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