Orthopaedic Device Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Orthopaedic Device Corp. makes
Orthopaedic Device Corp. manufactures femoral hemi-hip prostheses, including metal-backed acetabular cups designed for hip joint replacement. Their portfolio also includes a superfixation system for securing implants and a P.T.H. metal-backed acetabular cup for enhanced stability in orthopaedic procedures.
These devices are classified as Class II and Class III under FDA regulations, with authorisation primarily supported by 510(k) clearances. The company’s products are listed in the FDA’s 510(k) registry. Orthopaedic Device Corp. is based in the United States.
Catalogue
Femoral Hemi-Hip Prostheses Ref K855228
Regimes: 510(k) Registry: 510(k)Femoral Hemi-Hip Prosthesis Ref K862460
Regimes: 510(k) Registry: 510(k)Superfixation(Tm) Ref K863343
Regimes: 510(k) Registry: 510(k)P.T.H. Metal-Backed Acetabular Cup Ref K870234
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orthopaedic Device Corp. have in the registry?
The registry currently lists 4 devices for Orthopaedic Device Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orthopaedic Device Corp.'s devices?
Among its 4 most recently registered devices, Orthopaedic Device Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Orthopaedic Device Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Orthopaedic Device Corp.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Orthopaedic Device Corp. in the registry?
The most recently registered devices listed for Orthopaedic Device Corp. include FEMORAL HEMI-HIP PROSTHESES, FEMORAL HEMI-HIP PROSTHESIS, SUPERFIXATION(TM) and P.T.H. METAL-BACKED ACETABULAR CUP.