FDA 510(k) Applications Submitted by MONA INMAN
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K080185 |
01/25/2008 |
AMS ELEVATE WITH INTEPRO LITE PROLAPSE REPAIR SYSTEM, AMS ELEVATE WITH INTEXEN LP PROLAPSE REPAIR SYSTEM |
AMERICAN MEDICAL SYSTEMS, INC. |
| K111118 |
04/21/2011 |
AMS ELEVATE PC APICAL AND POSTERIOR ( AND ANTERIOR AND APICAL) PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE |
AMERICAN MEDICAL SYSTEMS |
| K082677 |
09/15/2008 |
AMS ELEVATE ANTERIOR & APICAL PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE |
AMERICAN MEDICAL SYSTEMS, INC. |
| K082730 |
09/18/2008 |
AMS ELEVATE APICAL AND POSTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE, AMS ELEVATE APICAL AND POSTERIOR PROLAPSE |
AMERICAN MEDICAL SYSTEMS, INC. |
| K073219 |
11/15/2007 |
WMT COLLAGEN DERMAL MATRIX, 4 CM X 7 CM, MODEL 89XM-4X07, VMT COLLAGEN DERMAL MATRIX, 6 CM X 8 CM, MODEL 89XM-6X08 |
AMERICAN MEDICAL SYSTEMS, INC. |
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