Centerplus Orthopedics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Centerplus Orthopedics, Inc. makes
Centerplus Orthopedics, Inc. manufactures modular tibial baseplates for knee replacements, including the cemented Natural-Knee II design, and anatomical shoulder prostheses with removable heads. These devices are intended for use in primary and revision orthopedic surgeries to restore joint function and stability.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) clearance pathway. These devices are intended for use within the United States, adhering to applicable FDA requirements for orthopedic implants.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Amatomical Shoulder With Removable Head Ref K030259
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Centerplus Orthopedics, Inc. have in the registry?
The registry currently lists 2 devices for Centerplus Orthopedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Centerplus Orthopedics, Inc.'s devices?
Among its 2 most recently registered devices, Centerplus Orthopedics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Centerplus Orthopedics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Centerplus Orthopedics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Centerplus Orthopedics, Inc. in the registry?
The most recently registered devices listed for Centerplus Orthopedics, Inc. include NATURAL-KNEE II CEMENTED MODULAR TIBIAL BASEPLATE and AMATOMICAL SHOULDER WITH REMOVABLE HEAD.