QLK — Stimulator, Neuromuscular, Lower Back Muscles, Totally Implanted For Pain Relief Class III

FDA Device Classification

FDA product code QLK covers "Stimulator, Neuromuscular, Lower Back Muscles, Totally Implanted 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
QLK
Device Class
Class III
Regulation Number
Submission Type
Review Panel
NE
Medical Specialty
Unknown
Implant
Yes

Definition

Stimulation of nerves that innervate muscles to treat or aid in the management of chronic, intractable lower back pain.