Medical Device Manufacturer · US , Newport Beach , CA

Apollo Spine, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2009

Total

Cleared

Denied

Apollo Spine, Inc. has 6 FDA 510(k) cleared medical devices. Based in Newport Beach, US.

Historical record: 6 cleared submissions from 2009 to 2012. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Apollo Spine, Inc.

6 devices

1-6 of 6