Cleared Special

K990197 - MODULUS COMPATIBLE STABILITY (MCS)-HA TOTAL HIP SYSTEM (FDA 510(k) Clearance)

Feb 1999
Decision
15d
Days
Class 2
Risk

K990197 is an FDA 510(k) clearance for the MODULUS COMPATIBLE STABILITY (MCS)-HA TOTAL HIP SYSTEM. This device is classified as a Prosthesis, Hip, Semi-constrained, Uncemented, Metal / Polymer, Non-porous, Calcium Phosphate (Class II - Special Controls, product code MEH).

Submitted by Exactech, Inc. (Gainesville, US). The FDA issued a Cleared decision on February 4, 1999, 15 days after receiving the submission on January 20, 1999.

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

Submission Details

510(k) Number K990197 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 20, 1999
Decision Date February 04, 1999
Days to Decision 15 days
Submission Type Special
Review Panel Orthopedic (OR)
Summary Summary PDF

Device Classification

Product Code MEH — Prosthesis, Hip, Semi-constrained, Uncemented, Metal / Polymer, Non-porous, Calcium Phosphate
Device Class Class II - Special Controls
CFR Regulation 21 CFR 888.3353

Similar Devices — MEH Prosthesis, Hip, Semi-constrained, Uncemented, Metal / Polymer, Non-porous, Calcium Phosphate

All 18
Allure Hip Stem and Intramedullary Plugs
K250375 · Waldemar Link GmbH & Co. KG · Nov 2025
Mfinity Femoral System
K251166 · Medacta International S.A. · Jun 2025
Trivicta® Hip Stem
K251052 · Ortho Development Corp. · May 2025
Resolve Modular Revision Hip Stem
K242315 · United Orthopedic Corporation · May 2025
Alteon® HA Femoral Stems
K243839 · Exactech, Inc. · Mar 2025
World Liner
K243162 · Signature Orthopaedics Pty, Ltd. · Nov 2024