510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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QGPNot classified

Posterior Ratcheting Rod System

Unknown
FDA source (opens on fda.gov)

QGP is the FDA product code for Posterior Ratcheting Rod System. FDA's definition for this code reads: "Stabilization or correction of adolescent idiopathic scoliosis without the use of fusion". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
QGP
Device name
Posterior Ratcheting Rod System
FDA definition
Stabilization or correction of adolescent idiopathic scoliosis without the use of fusion.
Device class
Not classified
Review panel
Unknown
Submission type
FDA code 6
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