Altus Partners, LLC
Altus Partners, LLC holds FDA 510(k) medical device clearances, first cleared 2015, most recent 2025.
Top product codes for Altus Partners, LLC
Recent clearances by Altus Partners, LLC
- K243419 — Altus Spine Navigation System
- K211027 — Altus Spine Pedicle Screw System
- K211837 — Altus Spine Interbody Standalone Fusion System
- K210887 — Altus Spine Sochi OCT Spinal System
- K200922 — Altus Spine HA Pedicle Screw System
- K200322 — Altus Spine Pedicle Screw System
- K183084 — Fuji Cervical Plate System
- K182406 — Altus Spine Interbody Fusion System
- K181339 — Altus Spine Pedicle Screw System
- K181281 — Altus Spine Pedicle Screw System
- K170553 — Altus Spine Interbody Fusion System
- K172253 — Altus Spine Cervical Interbody Fusion System
- K171329 — Altus Spine Titanium Interbody Fusion System
- K170512 — Altus Spine Titanium Interbody Fusion System
- K163061 — Altus Spine Cervical Plate System
- K160976 — Altus Spine Interbody Fusion System
- K151648 — Altus Spine Pedicle Screw System, Altus Spine MIS Pedicle Screw System, Valencia Pedicle Screw System, Valencia MIS Pedicle Screw System
Data sourced from openFDA. This site is unofficial and independent of the FDA.