FDA 510(k) Applications Submitted by Jenny Fam
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K172130 | 07/14/2017 | Resorbable Mesh Device | SeaSpine Orthopedics Corporation |
| K143448 | 12/02/2014 | Sonendo GentleWave System | Sonendo, Inc. |
| K103742 | 12/23/2010 | ACCELL EVO3 (FORMERLY ACCELL A2I) | INTEGRA LIFESCIENCES |
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