QGP — Posterior Ratcheting Rod System Class N

FDA Device Classification

FDA product code QGP covers "Posterior Ratcheting Rod System", a Class N medical device. Submissions are reviewed by the Unknown panel. Devices under this code are implants.

Classification Details

Product Code
QGP
Device Class
Class N
Regulation Number
Submission Type
Review Panel
OR
Medical Specialty
Unknown
Implant
Yes

Definition

Stabilization or correction of adolescent idiopathic scoliosis without the use of fusion.