Implanet

Implanet — FDA 510(k) Submissions

Implanet has submitted 3 FDA 510(k) premarket notifications since 2024, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Thoracolumbosacral Pedicle Screw System, Intervertebral Fusion Device With Bone Graft, Lumbar . Use the specialty filter in the sidebar to narrow results.