Cleared Special

K253314 - Freedom Infinia™ Total Knee System (FDA 510(k) Clearance)

Oct 2025
Decision
29d
Days
Class 2
Risk

K253314 is an FDA 510(k) clearance for the Freedom Infinia™ Total Knee System. This device is classified as a Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer (Class II - Special Controls, product code JWH).

Submitted by Maxx Orthopedics, Inc. (Norristown, US). The FDA issued a Cleared decision on October 29, 2025, 29 days after receiving the submission on September 30, 2025.

This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3560.

Submission Details

510(k) Number K253314 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 30, 2025
Decision Date October 29, 2025
Days to Decision 29 days
Submission Type Special
Review Panel Orthopedic (OR)
Summary Summary PDF

Device Classification

Product Code JWH — Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer
Device Class Class II - Special Controls
CFR Regulation 21 CFR 888.3560

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