Pro Surgical, Inc.

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

Pro Surgical, Inc. 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 Intervertebral Fusion Device With Integrated Fixation, Lumbar, Intervertebral Fusion Device With Integrated Fixation, Cervical . Use the specialty filter in the sidebar to narrow results.