FDA 510(k) Applications Submitted by Scott Rucker
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230808 | 03/23/2023 | PEEK SA Anterior Lumbar Interbody Fusion (ALIF) System | Kyocera Medical Technologies, Inc. |
| K212980 | 09/17/2021 | Tesera-k ALIF System | Kyocera Medical Technologies, Inc. |
| K223105 | 09/30/2022 | Tesera-K SC System | Kyocera Medical Technologies, Inc. |
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