Altus Partners, LLC
FDA 510(k) & PMA Approved Devices — 16 products
Total Devices16
Categories7
Latest Approval2025-05-08
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K243419 | Altus Spine Navigation System | OLO | 2025-05-08 | View |
| 510(k) | K211027 | Altus Spine Pedicle Screw System | NKB | 2022-09-16 | View |
| 510(k) | K211837 | Altus Spine Interbody Standalone Fusion System | OVD | 2022-04-19 | View |
| 510(k) | K210887 | Altus Spine Sochi OCT Spinal System | NKG | 2021-08-20 | View |
| 510(k) | K200922 | Altus Spine HA Pedicle Screw System | NKB | 2021-01-26 | View |
| 510(k) | K200322 | Altus Spine Pedicle Screw System | NKB | 2020-06-02 | View |
| 510(k) | K183084 | Fuji Cervical Plate System | KWQ | 2019-05-29 | View |
| 510(k) | K182406 | Altus Spine Interbody Fusion System | MAX | 2019-02-22 | View |
| 510(k) | K181339 | Altus Spine Pedicle Screw System | NKB | 2018-07-24 | View |
| 510(k) | K181281 | Altus Spine Pedicle Screw System | NKB | 2018-06-11 | View |
| 510(k) | K170553 | Altus Spine Interbody Fusion System | MAX | 2017-12-01 | View |
| 510(k) | K172253 | Altus Spine Cervical Interbody Fusion System | ODP | 2017-11-21 | View |
| 510(k) | K171329 | Altus Spine Titanium Interbody Fusion System | MAX | 2017-08-29 | View |
| 510(k) | K170512 | Altus Spine Titanium Interbody Fusion System | MAX | 2017-03-10 | View |
| 510(k) | K163061 | Altus Spine Cervical Plate System | KWQ | 2017-02-06 | View |
| 510(k) | K160976 | Altus Spine Interbody Fusion System | MAX | 2017-01-25 | View |
No matching devices.