Depuy Motech Acromed
Country not established
- Devices
- 4
What Depuy Motech Acromed makes
Depuy Motech Acromed manufactures spinal stabilization systems, including the DOC Ventral Cervical Stabilization System for anterior cervical support, the VSP System for posterior spinal fusion, and modular cage and interbody solutions like the Stackable Cage System and TIMX Low Back System for lumbar stabilization.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Doc Ventral Cervical Stabilization System Ref K982443
Regimes: 510(k) Registry: 510(k)Vsp System Ref K984350
Regimes: 510(k) Registry: 510(k)Stackable Cage System Ref K990148
Regimes: 510(k) Registry: 510(k)Timx Low Back System Ref K984348
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Depuy Motech Acromed have in the registry?
The registry currently lists 4 devices for Depuy Motech Acromed. Devices recorded under merged duplicate company entries are counted once.
Which registries list Depuy Motech Acromed's devices?
Among its 4 most recently registered devices, Depuy Motech Acromed has devices listed in FDA 510(k) (4 devices).
What risk classes do Depuy Motech Acromed's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Depuy Motech Acromed's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Depuy Motech Acromed in the registry?
The most recently registered devices listed for Depuy Motech Acromed include DOC VENTRAL CERVICAL STABILIZATION SYSTEM, VSP SYSTEM, STACKABLE CAGE SYSTEM and TIMX LOW BACK SYSTEM.