Reliance Medical Systems, LLC

Reliance Medical Systems, LLC — FDA 510(k) Submissions

Reliance Medical Systems, LLC has submitted 24 FDA 510(k) premarket notifications since 2007, of which 24 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Intervertebral Fusion Device With Bone Graft, Cervical, Orthosis, Spinal Pedicle Fixation, Intervertebral Fusion Device With Bone Graft, Lumbar, Appliance, Fixation, Spinal Intervertebral Body, Appliance, Fixation, Spinal Interlaminal . Use the specialty filter in the sidebar to narrow results.