Medical Device Manufacturer · US , Traverse City , MI

Spine Works

1 submissions · 1 cleared · Since 2001

Total

Cleared

Denied

Spine Works — FDA 510(k) Submissions

Spine Works has submitted 1 FDA 510(k) premarket notifications since 2001, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tong, Skull For Traction . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

SPINE WORKS COLLAR

K003662 · HAX Tong, Skull For Traction · Neurology

Jul 2001 223d

Spine Works

Spine Works — FDA 510(k) Submissions

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