FDA 510(k) Applications Submitted by SpineEX Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K190193 | 02/04/2019 | SpineEX Sagittae« Lateral Lumbar Interbody Fusion Devices | SpineEX Inc. |
| K181531 | 06/11/2018 | SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices | SpineEX Inc. |
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