Rti Surgical, Inc.

Rti Surgical, Inc. — FDA 510(k) Submissions

Rti Surgical, Inc. has submitted 7 FDA 510(k) premarket notifications since 2014, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Suture, Nonabsorbable, Synthetic, Polyethylene, Dura Substitute, Mesh, Surgical, Intervertebral Fusion Device With Bone Graft, Cervical, Intervertebral Fusion Device With Bone Graft, Lumbar . Use the specialty filter in the sidebar to narrow results.