Medical Device Manufacturer · US , Apple Valley , MN

Captiva Spine - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2012

Total

Cleared

Denied

Captiva Spine has 7 FDA 510(k) cleared medical devices. Based in Apple Valley, US.

Historical record: 7 cleared submissions from 2012 to 2016. Primary specialty: Orthopedic.

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

Regulatory submissions have been managed by Silver Spine Consulting, Silver Pine Consulting and Empirical Testing Corporation.

Captiva Spine is one of 18441 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Captiva Spine

7 devices

1-7 of 7