Northeast Iowa Podiatry
Country not established
- Devices
- 1
What Northeast Iowa Podiatry makes
Northeast Iowa Podiatry manufactures the T-SCREW, a surgical fixation device used in bone stabilization procedures, primarily within podiatric applications.
The T-SCREW is classified as a Class II medical device under FDA regulations and is supported by a 510(k) clearance. The company is based in the United States.
Catalogue
T-Screw Ref K851214
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Northeast Iowa Podiatry have in the registry?
The registry currently lists 1 device for Northeast Iowa Podiatry. Devices recorded under merged duplicate company entries are counted once.
Which registries list Northeast Iowa Podiatry's devices?
Among its 1 most recently registered device, Northeast Iowa Podiatry has devices listed in FDA 510(k) (1 device).
What risk classes do Northeast Iowa Podiatry's devices fall under?
Among its 1 most recently registered device, the classes recorded for Northeast Iowa Podiatry's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Northeast Iowa Podiatry in the registry?
The most recently registered devices listed for Northeast Iowa Podiatry include T-SCREW.