FDA 510(k) Applications Submitted by Spineology Inc
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160980 | 04/07/2016 | Threshold Pedicular Fixation System, Palisade Pedicular Fixation System | SPINEOLOGY INC |
| K182322 | 08/27/2018 | Duo Lumbar Interbody Fusion Device | Spineology Inc |
| K182345 | 08/28/2018 | Spineology Navigation Instruments | Spineology Inc |
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