Altus Partners, LLC - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Altus Partners, LLC has 17 FDA 510(k) cleared orthopedic devices. Based in Newtown Square, US.
Latest FDA clearance: May 2025. Active since 2015.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
17 devices
Cleared
May 08, 2025
Altus Spine Navigation System
Orthopedic
185d
Cleared
Sep 16, 2022
Altus Spine Pedicle Screw System
Orthopedic
528d
Cleared
Apr 19, 2022
Altus Spine Interbody Standalone Fusion System
Orthopedic
309d
Cleared
Aug 20, 2021
Altus Spine Sochi OCT Spinal System
Orthopedic
148d
Cleared
Jan 26, 2021
Altus Spine HA Pedicle Screw System
Orthopedic
295d
Cleared
Jun 02, 2020
Altus Spine Pedicle Screw System
Orthopedic
113d
Cleared
May 29, 2019
Fuji Cervical Plate System
Orthopedic
204d
Cleared
Feb 22, 2019
Altus Spine Interbody Fusion System
Orthopedic
171d
Cleared
Jul 24, 2018
Altus Spine Pedicle Screw System
Orthopedic
64d
Cleared
Jun 11, 2018
Altus Spine Pedicle Screw System
Orthopedic
27d
Cleared
Dec 01, 2017
Altus Spine Interbody Fusion System
Orthopedic
280d
Cleared
Nov 21, 2017
Altus Spine Cervical Interbody Fusion System
Orthopedic
118d
Cleared
Aug 29, 2017
Altus Spine Titanium Interbody Fusion System
Orthopedic
116d
Cleared
Mar 10, 2017
Altus Spine Titanium Interbody Fusion System
Orthopedic
17d
Cleared
Feb 06, 2017
Altus Spine Cervical Plate System
Orthopedic
97d
Cleared
Jan 25, 2017
Altus Spine Interbody Fusion System
Orthopedic
293d
Cleared
Oct 16, 2015
Altus Spine Pedicle Screw System, Altus Spine MIS Pedicle Screw System,...
Orthopedic
120d