Medical Device Manufacturer · US , Chesterland , OH

Paragon 28 - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2014

Recent clearances: HammerTube System

7
Total
7
Cleared
0
Denied

Paragon 28 has 7 FDA 510(k) cleared medical devices. Based in Chesterland, US.

Historical record: 7 cleared submissions from 2014 to 2018. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Paragon 28 Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Backroads Consulting, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Paragon 28

7 devices
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All7 Orthopedic 7