FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Freedom® Total Knee System – Titan PCK Components

K Number: K253144 · Decision Oct 22, 2025
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
23
Review Days
27

Basic Information

Device Name
Freedom® Total Knee System – Titan PCK Components
K Number
K253144
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Maxx Orthopedics, Inc.
Date Received
September 25, 2025
Decision Date
October 22, 2025
Product Code
JWH
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

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K Number Device Name
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K253314 Freedom Infinia™ Total Knee System
K243634 Maxx Libertas Bipolar Hip Head (Bipolar Hip)
K251717 Freedom® Total Knee System – Titanium Tibial Base Plate
K250382 Freedom Total Knee System (All-poly Tibial Plate)
K241597 Freedom® Total Knee System - Porous Tibial Base Plate
K243277 Freedom® Medial Congruent Liner
K240863 Freedom® Total Knee System
K200912 Freedom(R) - TiNbN Coated Knee
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