Zimvie Spine (Zimmer Biomet Spine, Inc.)
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Vital™ Spinal Fixation System Ref K240539
Regimes: 510(k) Registry: 510(k)Vital™ Navigation System Ref K233443
Regimes: 510(k) Registry: 510(k)Vital™ Spinal Fixation System Ref K230116
Regimes: 510(k) Registry: 510(k)Virage® Navigation System Ref K240647
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Zimvie Spine (Zimmer Biomet Spine, Inc.) have in the registry?
The registry currently lists 4 devices for Zimvie Spine (Zimmer Biomet Spine, Inc.). Devices recorded under merged duplicate company entries are counted once.
Which registries list Zimvie Spine (Zimmer Biomet Spine, Inc.)'s devices?
Among its 4 most recently registered devices, Zimvie Spine (Zimmer Biomet Spine, Inc.) has devices listed in FDA 510(k) (4 devices).
What risk classes do Zimvie Spine (Zimmer Biomet Spine, Inc.)'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Zimvie Spine (Zimmer Biomet Spine, Inc.)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Zimvie Spine (Zimmer Biomet Spine, Inc.) in the registry?
The most recently registered devices listed for Zimvie Spine (Zimmer Biomet Spine, Inc.) include Vital™ Spinal Fixation System, Vital™ Navigation System and Virage® Navigation System.