Zimmer Biomet Spine, Inc. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Zimmer Biomet Spine, Inc. has 15 FDA 510(k) cleared orthopedic devices. Based in Broomfield, US.
Last cleared in 2021. Active since 2017.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Zimmer Biomet Spine, Inc.
15 devices
Cleared
Aug 27, 2021
Virage Navigation System
Orthopedic
59d
Cleared
May 04, 2021
CaP Spheres Pellet Pack
Orthopedic
183d
Cleared
Apr 02, 2021
Polaris Spinal System
Orthopedic
60d
Cleared
Jan 28, 2021
Vitality® Spinal Fixation System
Orthopedic
59d
Cleared
Oct 08, 2020
Epic Anterior Thoracolumbar Plate System, Gallery Laminoplasty Fixation...
Orthopedic
55d
Cleared
Dec 02, 2019
Vital Navigation System
Orthopedic
158d
Cleared
Oct 29, 2019
Zimmer Biomet Universal Navigation System
Orthopedic
83d
Cleared
Oct 24, 2019
Zimmer Biomet Universal Navigation System
Orthopedic
233d
Cleared
Apr 08, 2019
Vitality® Spinal Fixation System
Orthopedic
109d
Cleared
Jan 15, 2019
Avenue P Cage System
Orthopedic
264d
Cleared
Mar 15, 2018
Polaris Spinal Growth System
Orthopedic
48d
Cleared
Feb 12, 2018
Zyston Strut Open Titanium Spacer System
Orthopedic
266d