Jmt Co., Ltd.

Jmt Co., Ltd. — FDA 510(k) Submissions

Jmt Co., Ltd. has submitted 4 FDA 510(k) premarket notifications since 2021, of which 4 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, Cervical, Catheter, Conduction, Anesthetic . Use the specialty filter in the sidebar to narrow results.