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Altus Partners, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
18
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243419Altus Spine Navigation SystemMay 8, 2025
K211027Altus Spine Pedicle Screw SystemSeptember 16, 2022
K211837Altus Spine Interbody Standalone Fusion SystemApril 19, 2022
K210887Altus Spine Sochi OCT Spinal SystemAugust 20, 2021
K200922Altus Spine HA Pedicle Screw SystemJanuary 26, 2021
K200322Altus Spine Pedicle Screw SystemJune 2, 2020
K183084Fuji Cervical Plate SystemMay 29, 2019
K182406Altus Spine Interbody Fusion SystemFebruary 22, 2019
K181339Altus Spine Pedicle Screw SystemJuly 24, 2018
K181281Altus Spine Pedicle Screw SystemJune 11, 2018
K170553Altus Spine Interbody Fusion SystemDecember 1, 2017
K172253Altus Spine Cervical Interbody Fusion SystemNovember 21, 2017
K171329Altus Spine Titanium Interbody Fusion SystemAugust 29, 2017
K170512Altus Spine Titanium Interbody Fusion SystemMarch 10, 2017
K163061Altus Spine Cervical Plate SystemFebruary 6, 2017
K160976Altus Spine Interbody Fusion SystemJanuary 25, 2017
K151648Altus Spine Pedicle Screw System, Altus Spine MIS Pedicle Screw System, Valencia Pedicle Screw SysteOctober 16, 2015
K132280ALTUS SPINE PEDICLE SCREW SYSTEMOctober 31, 2013