Freedom® Total Knee System – Titan PCK Components
K-Number: K253144 · 2025-10-22
Device Summary
Frequently Asked Questions
What is the Freedom® Total Knee System – Titan PCK Components?
Freedom® Total Knee System – Titan PCK Components is a medical device that received FDA 510(k) clearance on 2025-10-22. The listed applicant is Maxx Orthopedics, Inc.. The 510(k) number is K253144.
When did Freedom® Total Knee System – Titan PCK Components receive FDA 510(k) clearance?
Freedom® Total Knee System – Titan PCK Components received FDA 510(k) clearance on 2025-10-22, under 510(k) number K253144.
Who is the listed applicant for Freedom® Total Knee System – Titan PCK Components?
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 – Titan PCK Components?
The FDA product code for Freedom® Total Knee System – Titan PCK Components 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.