Freedom® Total Knee System – Titanium Tibial Base Plate (K251717)
Description
Freedom® Total Knee System – Titanium Tibial Base Plate by Maxx Orthopedics, Inc., an FDA 510(k) cleared orthopedic device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K251717
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Freedom® Total Knee System – Titanium Tibial Base Plate (K251717) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K241597 | Freedom® Total Knee System - Porous Tibial Base Plate | Maxx Orthopedics, Inc. | 2025 |
| K090411 | FREEDOM METAL BACKED TIBIAL COMPONENT | Maxx Orthopedics, Inc. | 2009 |
Trace the full predicate network for K251717
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.