Cleared Traditional

K250450 - Coated hip implants (FDA 510(k) Clearance)

Sep 2025
Decision
213d
Days
Class 2
Risk

K250450 is an FDA 510(k) clearance for the Coated hip implants. This device is classified as a Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented (Class II - Special Controls, product code LZO).

Submitted by Medacta International S.A. (Castel San Pietro, CH). The FDA issued a Cleared decision on September 19, 2025, 213 days after receiving the submission on February 18, 2025.

This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3353.

Submission Details

510(k) Number K250450 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 18, 2025
Decision Date September 19, 2025
Days to Decision 213 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF

Device Classification

Product Code LZO — Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented
Device Class Class II - Special Controls
CFR Regulation 21 CFR 888.3353

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