Skeletal Dynamics

Skeletal Dynamics — FDA 510(k) Submissions

Skeletal Dynamics has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Wrist, 3 Part Metal-plastic-metal Articulation, Semi-constrained . Use the specialty filter in the sidebar to narrow results.