FDA 510(k) Applications Submitted by K2M, Incorporated
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K161369 | 05/17/2016 | EVEREST Spinal System | K2M, Incorporated |
| K153031 | 10/19/2015 | RANGE/DENALI/MESA Spinal System | K2M, Incorporated |
| K153370 | 11/23/2015 | Caspian OCT/MESA Mini/DENALI Mini Spinal System | K2M, Incorporated |
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