Bethesda Medical Devices
Country not established
- Devices
- 2
What Bethesda Medical Devices makes
Bethesda Medical Devices manufactures the PRADO™ Lumbar Interbody Fusion System, a spinal implant designed for interbody fusion procedures in the lumbar spine.
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
Palisades™ Buttress Plate System Ref K261309
Regimes: 510(k) Registry: 510(k)PRADO™ Lumbar Interbody Fusion System Ref K252113
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bethesda Medical Devices have in the registry?
The registry currently lists 2 devices for Bethesda Medical Devices. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bethesda Medical Devices's devices?
Among its 2 most recently registered devices, Bethesda Medical Devices has devices listed in FDA 510(k) (2 devices).
What risk classes do Bethesda Medical Devices's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Bethesda Medical Devices's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bethesda Medical Devices in the registry?
The most recently registered devices listed for Bethesda Medical Devices include Palisades™ Buttress Plate System and PRADO™ Lumbar Interbody Fusion System.