Conmed Linvatec Biomaterials
FinlandFDA applicant, unverified
- Devices
- 1
What Conmed Linvatec Biomaterials makes
Conmed Linvatec Biomaterials manufactures interference screws designed for orthopedic fixation, including models like the MATRYX INTERFERENCE SCREW, which are used in joint stabilization procedures.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records in the FDA database. The company is based in the United States.
Catalogue
Matryx Interference Screw, 239038T5, 231025T5, 231033T5, 231038T5, 231125T5, 231133T5, 231138T5 Ref K063588
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Conmed Linvatec Biomaterials have in the registry?
The registry currently lists 1 device for Conmed Linvatec Biomaterials. Devices recorded under merged duplicate company entries are counted once.
Which registries list Conmed Linvatec Biomaterials's devices?
Among its 1 most recently registered device, Conmed Linvatec Biomaterials has devices listed in FDA 510(k) (1 device).
What risk classes do Conmed Linvatec Biomaterials's devices fall under?
Among its 1 most recently registered device, the classes recorded for Conmed Linvatec Biomaterials's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Conmed Linvatec Biomaterials in the registry?
The most recently registered devices listed for Conmed Linvatec Biomaterials include MATRYX INTERFERENCE SCREW, 239038T5, 231025T5, 231033T5, 231038T5, 231125T5, 231133T5, 231138T5.