FDA 510(k) Applications Submitted by Spinal Kinetics / Orthofix / SeaSpine
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K241117 | 04/23/2024 | M6-CÖ Single Use, Disposable Instrumentation | Spinal Kinetics / Orthofix / SeaSpine |
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