Cleared Special

Materialise Shoulder System?, Materialise Shoulder Guide and Models, SurgiCase Shoulder Planner

K241143 · Materialise NV · Orthopedic

May 2024

Decision

27d

Days

Class 2

Risk

About This 510(k) Submission

K241143 is an FDA 510(k) clearance for the Materialise Shoulder System?, Materialise Shoulder Guide and Models, SurgiCase Shoulder Planner, a Shoulder Arthroplasty Implantation System (Class II — Special Controls, product code QHE), submitted by Materialise NV (Leuven, BE). The FDA issued a Cleared decision on May 22, 2024, 27 days after receiving the submission on April 25, 2024. This device falls under the Orthopedic review panel. Regulated under 21 CFR 888.3660.

Submission Details

510(k) Number	K241143 FDA.gov
FDA Decision	Cleared SESE
Date Received	April 25, 2024
Decision Date	May 22, 2024
Days to Decision	27 days
Submission Type	Special
Review Panel	Orthopedic (OR)
Summary	Summary PDF

Device Classification

Product Code	QHE — Shoulder Arthroplasty Implantation System
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 888.3660
Definition	Intended To Be Used To Assist In The Implantation Of A Specific Shoulder Arthroplasty Device Or A Set Of Specific Shoulder Arthroplasty Devices. Indicated To Include Guiding Alignment, Making Or Establishing Cuts, Selecting, Sizing, Attaching, Positioning Or Orienting Implant Components.