J. Michael Putman, M.D., P.A.
Country not established
- Devices
- 2
What J. Michael Putman, M.D., P.A. makes
The company manufactures the Putman Stabilizer, a device designed for spinal stabilization procedures, likely intended for internal fixation in orthopedic surgery.
The Putman Stabilizer is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Putman Stabilizer Ref K915317
510(k) 510(k)Putman Stabilizer Ref K942584
510(k) 510(k)
Frequently asked questions
How many devices does J. Michael Putman, M.D., P.A. have in the registry?
The registry currently lists 2 devices for J. Michael Putman, M.D., P.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list J. Michael Putman, M.D., P.A.'s devices?
Among its 2 most recently registered devices, J. Michael Putman, M.D., P.A. has devices listed in FDA 510(k) (2 devices).
What risk classes do J. Michael Putman, M.D., P.A.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for J. Michael Putman, M.D., P.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from J. Michael Putman, M.D., P.A. in the registry?
The most recently registered devices listed for J. Michael Putman, M.D., P.A. include PUTMAN STABILIZER.