The Progressive Orthopaedic Company, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Progressive Orthopaedic Company, LLC - FDA 510(k) Cleared Devices
Recent clearances: The Progressive Orthopaedic Company Total Knee System II
5
Total
5
Cleared
0
Denied
The Progressive Orthopaedic Company, LLC has 5 FDA 510(k) cleared medical devices. Based in North Palm Beach, US.
Historical record: 5 cleared submissions from 2015 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by The Progressive Orthopaedic Company, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Progressive Orthopaedic Company, LLC
5 devices
Cleared
Mar 18, 2019
The Progressive Orthopaedic Company Total Knee System II
Orthopedic
105d
Cleared
Jul 27, 2016
The Progressive Orthopaedic Total Hip System
Orthopedic
426d
Cleared
Jun 23, 2015
Progressive Orthopaedic Total Knee System
Orthopedic
90d
Cleared
Mar 24, 2015
Progressive Orthopedic Total Knee System
Orthopedic
188d
Cleared
Feb 27, 2015
Progressive Orthopaedic Total Hip System
Orthopedic
100d