Medical Device Manufacturer · US , San Francisco , CA

Pontis Orthopaedics, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2014

Total

Cleared

Denied

Pontis Orthopaedics, LLC has 2 FDA 510(k) cleared medical devices. Based in San Francisco, US.

Historical record: 2 cleared submissions from 2014 to 2014. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Pontis Orthopaedics, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Pontis Orthopaedics, LLC

2 devices

1-2 of 2