FDA 510(k) Applications Submitted by Summit Spine
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K170572 | 02/27/2017 | Summit Spine Yellowstone Lumbar Interbody Fusion System | Summit Spine |
| K163494 | 12/13/2016 | Summit Spine Channel Cervical Interbody Fusion System | Summit Spine |
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