FDA 510(k) Applications Submitted by MARIE MARLOW
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K040070 | 01/14/2004 | ARTELON SPACER CMC-1 | ARTIMPLANT AB |
| K030656 | 03/03/2003 | ENVAN HEART RATE MONITOR | ENVAN, LLC |
| K052482 | 09/09/2005 | ARTELON SURGICAL SUTURE | ARTIMPLANT AB |
| K093753 | 12/07/2009 | MDPO FRAME SYSTEM | MDPO, LLC |
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