FDA 510(k) Applications Submitted by J. BRAD VANCE
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K031106 |
04/08/2003 |
IMTEC SENDAX MDI AND MDI PLUS ENDOSSEOUS IMPLANT, MODELS OB-XX, SH-XX, MOB-22, MSH-XX |
IMTEC CORP. |
K042289 |
08/24/2004 |
MDI ORTHO |
IMTEC CORP. |
K072660 |
09/21/2007 |
ENDURE IMPLANT, MODEL 5108, 5111, 5113, 5114 |
IMTEC CORP. |
K053046 |
10/28/2005 |
ILUMA ORTHOCAT/DENTALCAT |
IMTEC CORP. |
K043226 |
11/22/2004 |
ENDURE IMPLANT, MODELS 3508, 4308, 3520, 4320 |
IMTEC CORP. |
K030243 |
01/23/2003 |
ENDURE IMPLANT, MODEL 3508,3511,3514,4308,4311,4314 |
IMTEC CORP. |
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