Mircoport Orthopedics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mircoport Orthopedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EVOLUTION NitrX Medial-Pivot Knee
1
Total
1
Cleared
0
Denied
Mircoport Orthopedics, Inc. has 1 FDA 510(k) cleared medical devices. Based in Arlington, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Mircoport Orthopedics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mircoport Orthopedics, Inc.
1 devices