Osteospring Medical, Inc.
Country not established
- Devices
- 1
What Osteospring Medical, Inc. makes
Osteospring Medical, Inc. manufactures the Osteospring FootJack Subtalar Implant System, a device designed for subtalar joint arthrodesis to address conditions such as chronic pain or instability in the foot’s hindfoot region.
The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) premarket notifications. The manufacturer is based in the United States.
Catalogue
Osteospring Footjack Subtalar Implant System Ref K112658
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Osteospring Medical, Inc. have in the registry?
The registry currently lists 1 device for Osteospring Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Osteospring Medical, Inc.'s devices?
Among its 1 most recently registered device, Osteospring Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Osteospring Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Osteospring Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Osteospring Medical, Inc. in the registry?
The most recently registered devices listed for Osteospring Medical, Inc. include OSTEOSPRING FOOTJACK SUBTALAR IMPLANT SYSTEM.