Stryker Spine - FDA 510(k) Cleared Devices
74
Total
73
Cleared
0
Denied
Stryker Spine has 73 FDA 510(k) cleared orthopedic devices. Based in Allendale, US.
Latest FDA clearance: Apr 2026. Active since 2004.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
74 devices
Cleared
Apr 24, 2026
Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip
Orthopedic
29d
Cleared
Nov 07, 2024
OZARK Cervical Plate System
Orthopedic
90d
Cleared
Aug 29, 2024
Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip, Vitoss® BiModal...
Orthopedic
27d
Cleared
Jun 08, 2023
XIA® 4.5 Spinal System, XIA® 4.5 Cortical Trajectory, XIA® 3 Spinal System,...
Orthopedic
275d
Cleared
Feb 14, 2023
Tritanium C Anterior Cervical Cage, Tritanium PL Cage, Tritanium TL Curved...
Orthopedic
267d
Cleared
Mar 23, 2021
Navigated Spine Instruments
Orthopedic
144d
Cleared
Apr 23, 2020
Stryker Xia 3 Power Adaptor
Orthopedic
41d
Cleared
Jul 25, 2019
Tritanium X PL Expandable Posterior Lumbar Cage, Tritanium X TL Expandable...
Orthopedic
246d
Cleared
Jan 10, 2019
VLIFT-s Vertebral Body Replacement System
Orthopedic
66d
Cleared
Jul 18, 2018
Tritanium PL Cage
Orthopedic
92d
Cleared
Sep 06, 2017
Tritanium C Anterior Cervical Cage
Orthopedic
107d
Cleared
Jul 15, 2016
Ascential IBD PEEKc Spacer
Orthopedic
56d
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