Microport Orthopedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EVOLUTION® AM BIOFOAM® Tibial System, NEXUS® Hip Stem, Evolution® Total Knee Systems - Kinematic Alignment Instrumentation and Technique
38
Total
38
Cleared
0
Denied
FDA 510(k) Regulatory Record - Microport Orthopedics, Inc. Orthopedic ✕
38 devices
Cleared
Aug 21, 2026
EVOLUTION® AM BIOFOAM® Tibial System
Orthopedic
270d
Cleared
May 15, 2025
NEXUS® Hip Stem
Orthopedic
90d
Cleared
Feb 18, 2025
Evolution® Total Knee Systems - Kinematic Alignment Instrumentation and...
Orthopedic
91d
Cleared
Apr 12, 2024
Ceramic Femoral Head
Orthopedic
57d
Cleared
Apr 01, 2024
EVOLUTION® Hinge Knee System
Orthopedic
87d
Cleared
Jan 18, 2024
EVOLUTION® Tibial Cones
Orthopedic
79d
Cleared
Oct 31, 2023
EVOLUTION® Cement Keel
Orthopedic
123d
Cleared
Sep 27, 2023
EVOLUTION® Hinge Knee System
Orthopedic
210d
Cleared
Jan 05, 2022
MPO Hip Instruments
Orthopedic
29d
Cleared
Jan 05, 2022
MPO Knee Instruments
Orthopedic
29d
Cleared
Oct 01, 2021
E-CLASS® DUAL MOBILITY INSERTS and DYNASTY® DUAL MOBILITY LINERS
Orthopedic
638d
Cleared
Aug 24, 2021
Prime BIOFOAM® Multi-Hole Shells
Orthopedic
481d
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