FDA 510(k) Applications Submitted by LANTERNA MEDICAL TECHNOLOGIES
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K150507 | 02/26/2015 | Santis Pedicle Screw System | LANTERNA MEDICAL TECHNOLOGIES |
| K133063 | 09/27/2013 | SANTIS PEDICLE SCREW SYSTEM | LANTERNA MEDICAL TECHNOLOGIES |
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