Spine Works
Country not established
- Devices
- 5
What Spine Works makes
Spine Works manufactures the Spine Works Collar, a cervical orthotic device designed for immobilization and support of the neck region.
The Spine Works Collar is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Spineworks Anterior Lumbar Device Ref K133340
Regimes: 510(k) Registry: 510(k)Fixxsure Cross Link Ref K081331
Regimes: 510(k) Registry: 510(k)Stansion Matrix Ref K042600
Regimes: 510(k) Registry: 510(k)Spine Works Collar Ref K003662
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spine Works have in the registry?
The registry currently lists 5 devices for Spine Works. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spine Works's devices?
Among its 5 most recently registered devices, Spine Works has devices listed in FDA 510(k) (5 devices).
What risk classes do Spine Works's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Spine Works's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spine Works in the registry?
The most recently registered devices listed for Spine Works include A-WEDGE ANTERIOR INTERBODY SYSTEM (A-WEDGE A.I.S.), SPINEWORKS ANTERIOR LUMBAR DEVICE, FIXXSURE CROSS LINK and STANSION MATRIX.