FDA 510(k) Applications Submitted by KEITH CANNAN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K172086 | 07/11/2017 | MatiraÖ Anterior Cervical System | Kalitec Direct, LLC |
| K163471 | 12/12/2016 | Kalitec Direct InSePtionÖ MIS Fixation System | KALITEC DIRECT, LLC |
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