PMP — Dorsal Root Ganglion Stimulator For Pain Relief Class III

FDA Device Classification

FDA product code PMP covers "Dorsal Root Ganglion Stimulator For Pain Relief", a Class III medical device. Submissions are reviewed by the Unknown panel. Devices under this code are implants.

Classification Details

Product Code
PMP
Device Class
Class III
Regulation Number
Submission Type
Review Panel
NE
Medical Specialty
Unknown
Implant
Yes

Definition

Stimulation of the dorsal root ganglion for the treatment of chronic, intractable pain of the lower limbs.