Tasarimmed Tibbi Mamuller Sanayi VE Ticaret A.S
TürkiyeFDA applicant, unverified
- Devices
- 1
What Tasarimmed Tibbi Mamuller Sanayi VE Ticaret A.S makes
Tasarimmed Tibbi Mamuller Sanayi VE Ticaret A.S manufactures the Spider Frame External Fixation System, a device used for stabilizing and supporting bone fractures through external fixation techniques.
The Spider Frame External Fixation System is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the US.
Catalogue
Spider Frame External Fixation System Ref K170482
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tasarimmed Tibbi Mamuller Sanayi VE Ticaret A.S have in the registry?
The registry currently lists 1 device for Tasarimmed Tibbi Mamuller Sanayi VE Ticaret A.S. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tasarimmed Tibbi Mamuller Sanayi VE Ticaret A.S's devices?
Among its 1 most recently registered device, Tasarimmed Tibbi Mamuller Sanayi VE Ticaret A.S has devices listed in FDA 510(k) (1 device).
What risk classes do Tasarimmed Tibbi Mamuller Sanayi VE Ticaret A.S's devices fall under?
Among its 1 most recently registered device, the classes recorded for Tasarimmed Tibbi Mamuller Sanayi VE Ticaret A.S's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tasarimmed Tibbi Mamuller Sanayi VE Ticaret A.S in the registry?
The most recently registered devices listed for Tasarimmed Tibbi Mamuller Sanayi VE Ticaret A.S include Spider Frame External Fixation System.