Frontier Medical Devices, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Frontier Medical Devices, Inc. makes
Frontier Medical Devices, Inc. manufactures spinal and orthopedic hardware, including interbody fusion devices, posterior cable screw systems, and in-line orthopedic cable cerclage systems.
These Class II medical devices are based in the United States and are listed within the FDA 510(k) regulatory registry.
Catalogue
Frontier Sadl Interbody Fusion Device Ref K112700
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Ancora LLC Interbody Fusion Device Ref K143228
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Frontier Medical Devices, Inc. have in the registry?
The registry currently lists 5 devices for Frontier Medical Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Frontier Medical Devices, Inc.'s devices?
Among its 5 most recently registered devices, Frontier Medical Devices, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Frontier Medical Devices, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Frontier Medical Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Frontier Medical Devices, Inc. in the registry?
The most recently registered devices listed for Frontier Medical Devices, Inc. include FRONTIER SADL INTERBODY FUSION DEVICE, Frontier Medical Devices Posterior Cable Screw System, Frontier Medical Devices In-line Orthopedic Cable Cerclage System and Ancora LLC Interbody Fusion Device.