Altus Partners
Altus Partners appears in FDA public data with 0 recalls, 18 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 8, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 18
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K243419 | Altus Spine Navigation System | May 8, 2025 |
| K211027 | Altus Spine Pedicle Screw System | Sep 16, 2022 |
| K211837 | Altus Spine Interbody Standalone Fusion System | Apr 19, 2022 |
| K210887 | Altus Spine Sochi OCT Spinal System | Aug 20, 2021 |
| K200922 | Altus Spine HA Pedicle Screw System | Jan 26, 2021 |
| K200322 | Altus Spine Pedicle Screw System | Jun 2, 2020 |
| K183084 | Fuji Cervical Plate System | May 29, 2019 |
| K182406 | Altus Spine Interbody Fusion System | Feb 22, 2019 |
| K181339 | Altus Spine Pedicle Screw System | Jul 24, 2018 |
| K181281 | Altus Spine Pedicle Screw System | Jun 11, 2018 |
| K170553 | Altus Spine Interbody Fusion System | Dec 1, 2017 |
| K172253 | Altus Spine Cervical Interbody Fusion System | Nov 21, 2017 |
| K171329 | Altus Spine Titanium Interbody Fusion System | Aug 29, 2017 |
| K170512 | Altus Spine Titanium Interbody Fusion System | Mar 10, 2017 |
| K163061 | Altus Spine Cervical Plate System | Feb 6, 2017 |
| K160976 | Altus Spine Interbody Fusion System | Jan 25, 2017 |
| K151648 | Altus Spine Pedicle Screw System, Altus Spine MIS Pedicle Screw System, Valencia Pedicle Screw Syste | Oct 16, 2015 |
| K132280 | ALTUS SPINE PEDICLE SCREW SYSTEM | Oct 31, 2013 |