Burdette Medical Systems, Inc.
Country not established
- Devices
- 1
What Burdette Medical Systems, Inc. makes
Burdette Medical Systems, Inc. manufactures the INTERPLANT, a device designed for interplantar (heel) pressure measurement, commonly used in clinical settings to assess plantar pressure distribution.
The INTERPLANT is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
Interplant Ref K982696
510(k) 510(k)
Frequently asked questions
How many devices does Burdette Medical Systems, Inc. have in the registry?
The registry currently lists 1 device for Burdette Medical Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Burdette Medical Systems, Inc.'s devices?
Among its 1 most recently registered device, Burdette Medical Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Burdette Medical Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Burdette Medical Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Burdette Medical Systems, Inc. in the registry?
The most recently registered devices listed for Burdette Medical Systems, Inc. include INTERPLANT.