FDA 510(k) Applications Submitted by KELLI J ANDERSON
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K060041 |
01/06/2006 |
TRIMED BONE PLATES |
TRIMED, INC. |
| K050681 |
03/16/2005 |
OMNITECH SYSTEM & EASY LOCK OSTEOSYSTEM WITH XTREMITIES PLATES |
TRIMED, INC. |
| K091156 |
04/21/2009 |
TRIMED STERILE PRODUCT |
TRIMED, INC. |
| K081348 |
05/14/2008 |
TENODESIS CROSS SCREW, INTERFERENCE SCREW, SUTURE BEAD |
TRIMED, INC. |
| K101375 |
05/17/2010 |
TRIMED X-FIX |
TRIMED, INC. |
| K071876 |
07/06/2007 |
CROSS.BONE |
TRIMED, INC. |
| K113369 |
11/15/2011 |
ZIMMER PERSONA KNEE SYSTEM |
ZIMMER INC. |
| K043263 |
11/24/2004 |
TRIMED OSTEOTOMY PLATE |
TRIMED, INC. |
| K093676 |
11/27/2009 |
OMNITECH LARGE, TRIMED COMPRESSION SCREW |
TRIMED, INC. |
| K121771 |
06/15/2012 |
ZIMMER PERSONA THE PERSONALIZED KNEE SYSTEM |
ZIMMER, INC. |
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