Medical Device Manufacturer · US , Traverse City , MI

Spine Works - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2001

Total

Cleared

Denied

Spine Works has 1 FDA 510(k) cleared medical devices. Based in Traverse City, US.

Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: Neurology.

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

Spine Works is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Spine Works

1 devices

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