FDA 510(k) Applications Submitted by Adam Deitz
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K171617 | 06/01/2017 | OKI Surgical Planning Software | Ortho Kinematics, Inc. |
| K172327 | 08/01/2017 | VMAÖ System version 3.0 | Ortho Kinematics, Inc. |
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