FDA 510(k) Applications Submitted by FloSpine
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K210182 | 01/25/2021 | PANAMAÖ Anterior Cervical Plate (ACP) System | FloSpine |
| K223231 | 10/18/2022 | Ti-Largo Cervical Interbody System | FloSpine |
| K141850 | 07/09/2014 | FLOSPINE PEDICLE SCREW SYSTEM | FLOSPINE |
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