FDA 510(k) Applications Submitted by VORTEK SURGICAL, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K080341 | 02/08/2008 | ENDODRAPE(TM) | VORTEK SURGICAL, LLC |
| K070406 | 02/12/2007 | ENDODRAPE | VORTEK SURGICAL, LLC |
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