FDA 510(k) Applications Submitted by AMY CONUEL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K080778 | 03/19/2008 | ENSPLINT TM BONE SCREW | SONOMA ORTHOPEDIC PRODUCTS, INC. |
| K092401 | 08/06/2009 | SINEXUS SINUS STENT GEN 2, MODEL 1999-25 | SINEXUS, INC. |
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