QLKClass III

Stimulator, Neuromuscular, Lower Back Muscles, Totally Implanted For Pain Relief

Unknown

QLK is the FDA product code for Stimulator, Neuromuscular, Lower Back Muscles, Totally Implanted For Pain Relief, a class III device type. FDA's definition for this code reads: "Stimulation of nerves that innervate muscles to treat or aid in the management of chronic, intractable lower back pain". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: QLK
Device name: Stimulator, Neuromuscular, Lower Back Muscles, Totally Implanted For Pain Relief
FDA definition: Stimulation of nerves that innervate muscles to treat or aid in the management of chronic, intractable lower back pain.
Device class: Class III
Review panel: Unknown
Submission type: PMA
Implant: Yes
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 0

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code QLK

FDA records hold no clearances under product code QLK.

Recent recalls

Product code QLK

FDA records show no recalls under product code QLK.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)