Spinesmith Partners, LLP
Country not established
- Devices
- 1
What Spinesmith Partners, LLP makes
Spinesmith Partners, LLC manufactures the SOLUM IV Bone Void Filler, a product designed to fill bone voids in spinal surgeries, promoting structural integrity and bone regeneration.
The SOLUM IV Bone Void Filler is classified as a Class II medical device in the US and is listed under FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Solum Iv Bone Void Filler Ref K132470
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spinesmith Partners, Llp have in the registry?
The registry currently lists 1 device for Spinesmith Partners, Llp. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spinesmith Partners, Llp's devices?
Among its 1 most recently registered device, Spinesmith Partners, Llp has devices listed in FDA 510(k) (1 device).
What risk classes do Spinesmith Partners, Llp's devices fall under?
Among its 1 most recently registered device, the classes recorded for Spinesmith Partners, Llp's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spinesmith Partners, Llp in the registry?
The most recently registered devices listed for Spinesmith Partners, Llp include SOLUM IV BONE VOID FILLER.