Medical Device Manufacturer · US , Andover , MA

Smith & Newphew, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2010

Total

Cleared

Denied

Smith & Newphew, Inc. has 2 FDA 510(k) cleared medical devices. Based in Andover, US.

Historical record: 2 cleared submissions from 2010 to 2011. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Smith & Newphew, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Smith & Newphew, Inc.

2 devices

1-2 of 2