FDA 510(k) Applications Submitted by LAURA LEBOEUF
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K101085 | 04/19/2010 | SPINESMITH CYNCH SPINAL SYSTEM | SPINE SMITH PARTNERS L.P. |
| K102090 | 07/26/2010 | SPINESMITH CYNCH SPINAL SYSTEM - VISUALIF INTERBODY FUSION IMPLANT SYSTEM | SPINE SMITH PARTNERS L.P. |
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