PHM

Intervertebral Fusion Device With Bone Graft, Thoracic

Product code

PHM

Device name

Intervertebral Fusion Device With Bone Graft, Thoracic

Device class

Class 2

21 CFR

21 CFR 888.3080

Medical specialty

Orthopedic

Marketing pathway

510(K)

Flag

Implant

510(k) clearances (all years, FDA)

3 (all years; only the last 3 years are listed here)

FDA classification definition

Intended to stabilize thoracic spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft.

Definition text from the FDA device classification database (U.S. federal government work, public domain).