Accelerated Innovation, LLC
United StatesFDA applicant, unverified
- Devices
- 7
What Accelerated Innovation, LLC makes
Accelerated Innovation, LLC manufactures orthopedic implant systems including anterior cervical plate systems, pedicle screw systems, patellofemoral systems, total knee systems, unipolar head systems, hip systems, and bipolar head systems.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Accin Anterior Cervical Plate System Ref K073530
Regimes: 510(k) Registry: 510(k)Accin Pedicle Screw System Ref K073531
Regimes: 510(k) Registry: 510(k)Accin Patellofemoral System Ref K073120
Regimes: 510(k) Registry: 510(k)Accin Total Knee System Ref K081127
Regimes: 510(k) Registry: 510(k)Accin Unipolar Head System Ref K080539
Regimes: 510(k) Registry: 510(k)Accin Hip System Ref K073068
Regimes: 510(k) Registry: 510(k)Accin Bipolar Head System Ref K080647
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Accelerated Innovation, LLC have in the registry?
The registry currently lists 7 devices for Accelerated Innovation, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Accelerated Innovation, LLC's devices?
Among its 7 most recently registered devices, Accelerated Innovation, LLC has devices listed in FDA 510(k) (7 devices).
What risk classes do Accelerated Innovation, LLC's devices fall under?
Among its 7 most recently registered devices, the classes recorded for Accelerated Innovation, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Accelerated Innovation, LLC in the registry?
The most recently registered devices listed for Accelerated Innovation, LLC include ACCIN ANTERIOR CERVICAL PLATE SYSTEM, ACCIN PEDICLE SCREW SYSTEM, ACCIN PATELLOFEMORAL SYSTEM and ACCIN TOTAL KNEE SYSTEM.