FDA 510(k) Applications Submitted by Scott Peterson
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K212450 | 08/05/2021 | Keos Anterior Cervical Interbody Fusion Device System | Keos |
| K193174 | 11/18/2019 | Keos Lumbar IBFD | Keos |
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