FDA 510(k) Applications Submitted by Anne-Marie Keefe
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K163034 | 10/31/2016 | SUTUREFIX Curved Suture Anchor | Smith and Nephew, Inc. |
| K173901 | 12/22/2017 | MyoSure MANUAL Tissue Removal Device | Hologic, Inc. |
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