Freedom® Total Knee System – Titanium Tibial Base Plate
K-Number: K251717 · 2025-06-26
Device Summary
Frequently Asked Questions
What is the Freedom® Total Knee System – Titanium Tibial Base Plate?
Freedom® Total Knee System – Titanium Tibial Base Plate is a medical device that received FDA 510(k) clearance on 2025-06-26. The listed applicant is Maxx Orthopedics, Inc.. The 510(k) number is K251717.
When did Freedom® Total Knee System – Titanium Tibial Base Plate receive FDA 510(k) clearance?
Freedom® Total Knee System – Titanium Tibial Base Plate received FDA 510(k) clearance on 2025-06-26, under 510(k) number K251717.
Who is the listed applicant for Freedom® Total Knee System – Titanium Tibial Base Plate?
The FDA 510(k) record lists Maxx Orthopedics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Freedom® Total Knee System – Titanium Tibial Base Plate?
The FDA product code for Freedom® Total Knee System – Titanium Tibial Base Plate is JWH.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Maxx Orthopedics, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: JWH)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.