FDA 510(k) Applications Submitted by ALTUS PARTNERS, LLC
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K170512 |
02/21/2017 |
Altus Spine Titanium Interbody Fusion System |
Altus Partners, LLC |
| K160976 |
04/07/2016 |
Altus Spine Interbody Fusion System |
ALTUS PARTNERS, LLC |
| K171329 |
05/05/2017 |
Altus Spine Titanium Interbody Fusion System |
Altus Partners, LLC |
| K151648 |
06/18/2015 |
Altus Spine Pedicle Screw System, Altus Spine MIS Pedicle Screw System, Valencia Pedicle Screw System, Valencia MIS Pedicle Screw System |
Altus Partners, LLC |
| K163061 |
11/01/2016 |
Altus Spine Cervical Plate System |
Altus Partners, LLC |
| 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 |
| 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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