FDA 510(k) Applications Submitted by Bluestone Synergy
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K171893 | 06/26/2017 | Blustone Synergy Lumbar Interbody Fusion System (Basalt, Magma, Obsidian), Blustone Synergy Cervical Interbody Fusion System (Slate) | Bluestone Synergy |
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