FDA 510(k) Applications Submitted by Bodycad Laboratories Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K181302 | 05/17/2018 | Bodycad Unicompartmental Knee System | Bodycad Laboratories Inc. |
| K240066 | 01/09/2024 | Fine OsteotomyÖ | Bodycad Laboratories Inc. |
| K241356 | 05/14/2024 | Fine OsteotomyÖ | Bodycad Laboratories Inc. |
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