Specialty Spine Products, LLC
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ssp Vertebral Body Replacement Ref K061578
Regimes: 510(k) Registry: 510(k)Ssp Pedicle Screw System Ref K060118
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Specialty Spine Products, LLC have in the registry?
The registry currently lists 2 devices for Specialty Spine Products, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Specialty Spine Products, LLC's devices?
Among its 2 most recently registered devices, Specialty Spine Products, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Specialty Spine Products, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Specialty Spine Products, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Specialty Spine Products, LLC in the registry?
The most recently registered devices listed for Specialty Spine Products, LLC include SSP VERTEBRAL BODY REPLACEMENT and SSP PEDICLE SCREW SYSTEM.