FDA 510(k) Applications Submitted by Blustone Synergy, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K210382 | 02/09/2021 | Blustone Synergy Diamond SA Cervical System | Blustone Synergy, LLC |
| K203520 | 12/01/2020 | Blustone Synergy Interbody Fusion System | Blustone Synergy, LLC |
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