FDA 510(k) Applications Submitted by Mark Melton
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K200322 |
02/10/2020 |
Altus Spine Pedicle Screw System |
Altus Partners, LLC |
| K170553 |
02/24/2017 |
Altus Spine Interbody Fusion System |
Altus Partners, LLC |
| K210887 |
03/25/2021 |
Altus Spine Sochi OCT Spinal System |
Altus Partners, LLC |
| K200922 |
04/06/2020 |
Altus Spine HA Pedicle Screw System |
Altus Partners, LLC |
| K211027 |
04/06/2021 |
Altus Spine Pedicle Screw System |
Altus Partners, LLC |
| K181281 |
05/15/2018 |
Altus Spine Pedicle Screw System |
Altus Partners, LLC |
| K181339 |
05/21/2018 |
Altus Spine Pedicle Screw System |
Altus Partners, LLC |
| K211837 |
06/14/2021 |
Altus Spine Interbody Standalone Fusion System |
Altus Partners, LLC |
| K232059 |
07/11/2023 |
Tympanostomy Tubes |
Grace Medical, Inc. |
| K172253 |
07/26/2017 |
Altus Spine Cervical Interbody Fusion System |
Altus Partners, LLC |
| K182406 |
09/04/2018 |
Altus Spine Interbody Fusion System |
Altus Partners, LLC |
| K183084 |
11/06/2018 |
Fuji Cervical Plate System |
Altus Partners, LLC |
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