Medical Device Manufacturer · US , Carlsnad , CA

Alphatec Spine - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2016

Total

Cleared

Denied

Alphatec Spine has 6 FDA 510(k) cleared medical devices. Based in Carlsnad, US.

Latest FDA clearance: Sep 2025. Active since 2016. Primary specialty: Orthopedic.

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

510(k) submissions have been managed by Alphatec Spine, Inc. as regulatory consultant.

Alphatec Spine is one of 16135 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Alphatec Spine

6 devices

1-6 of 6