Sinaptic Surgical
Country not established
- Devices
- 1
What Sinaptic Surgical makes
Sinaptic Surgical manufactures the Osteotomy Wedge System, a surgical implant designed for bone realignment procedures, including corrective osteotomies.
The company’s portfolio is regulated under FDA Class II devices and is listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Osteotomy Wedge System Ref K252254
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sinaptic Surgical have in the registry?
The registry currently lists 1 device for Sinaptic Surgical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sinaptic Surgical's devices?
Among its 1 most recently registered device, Sinaptic Surgical has devices listed in FDA 510(k) (1 device).
What risk classes do Sinaptic Surgical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Sinaptic Surgical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sinaptic Surgical in the registry?
The most recently registered devices listed for Sinaptic Surgical include Osteotomy Wedge System.