Cleared Traditional

K251618 - MOTO Partial Knee System Extension (FDA 510(k) Clearance)

Jul 2025
Decision
58d
Days
Class 2
Risk

K251618 is an FDA 510(k) clearance for the MOTO Partial Knee System Extension. This device is classified as a Prosthesis, Knee, Femorotibial, Non-constrained, Cemented, Metal/polymer (Class II - Special Controls, product code HSX).

Submitted by Medacta International S.A. (Castel San Pietro, CH). The FDA issued a Cleared decision on July 24, 2025, 58 days after receiving the submission on May 27, 2025.

This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3520.

Submission Details

510(k) Number K251618 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 27, 2025
Decision Date July 24, 2025
Days to Decision 58 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF

Device Classification

Product Code HSX — Prosthesis, Knee, Femorotibial, Non-constrained, Cemented, Metal/polymer
Device Class Class II - Special Controls
CFR Regulation 21 CFR 888.3520

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