Curiteva, Inc.

Curiteva, Inc. — FDA 510(k) Submissions

Curiteva, Inc. has submitted 11 FDA 510(k) premarket notifications since 2019, of which 11 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, Spine, Plate, Laminoplasty, Metal, Intervertebral Fusion Device With Integrated Fixation, Lumbar, Thoracolumbosacral Pedicle Screw System, Sacroiliac Joint Fixation . Use the specialty filter in the sidebar to narrow results.