Adaptive Specialty, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Adaptive Specialty, LLC makes
Adaptive Specialty, LLC manufactures spinal interbody fusion cages, including cervical and lumbar models designed for anterior cervical and lumbar spine procedures. The company also produces the Adaptive Wedge, a device intended for spinal stabilization applications.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Adaptive Wedge Ref K110662
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Adaptive Specialty, LLC have in the registry?
The registry currently lists 2 devices for Adaptive Specialty, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Adaptive Specialty, LLC's devices?
Among its 2 most recently registered devices, Adaptive Specialty, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Adaptive Specialty, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Adaptive Specialty, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Adaptive Specialty, LLC in the registry?
The most recently registered devices listed for Adaptive Specialty, LLC include FUSION ADVANTAGE CERVICAL CAGE, FUSION ADVANTAGE LUMBAR CAGE and ADAPTIVE WEDGE.