Depuy Synthes Spine
Country not established
- Devices
- 3
What Depuy Synthes Spine makes
Depuy Synthes Spine manufactures spinal fixation and interbody fusion devices, including the SYNMESH System for mesh reinforcement and the DePuy Synthes T-PAL Spacer System for intervertebral support.
These products are classified as Class II medical devices under FDA regulations and are authorised via the 510(k) pathway. The company operates from the United States.
Catalogue
SYNMESH System Ref K183054
510(k) 510(k)Vertical Expandable Prosthetic Titanium Rib Ref K142587
510(k) 510(k)DePuy Synthes T-PAL Spacer System Ref K181231
510(k) 510(k)
Frequently asked questions
How many devices does Depuy Synthes Spine have in the registry?
The registry currently lists 3 devices for Depuy Synthes Spine. Devices recorded under merged duplicate company entries are counted once.
Which registries list Depuy Synthes Spine's devices?
Among its 3 most recently registered devices, Depuy Synthes Spine has devices listed in FDA 510(k) (3 devices).
What risk classes do Depuy Synthes Spine's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Depuy Synthes Spine's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Depuy Synthes Spine in the registry?
The most recently registered devices listed for Depuy Synthes Spine include SYNMESH System, Vertical Expandable Prosthetic Titanium Rib and DePuy Synthes T-PAL Spacer System.