Medical Device Manufacturer · US , Portage , MI

Stryker Craniomaxillofacial

3 submissions · 3 cleared · Since 2007
3
Total
3
Cleared
0
Denied

Stryker Craniomaxillofacial — FDA 510(k) Submissions

Stryker Craniomaxillofacial has submitted 3 FDA 510(k) premarket notifications since 2007, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Plate, Bone, Drills, Burrs, Trephines & Accessories (simple, Powered) . Use the specialty filter in the sidebar to narrow results.

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