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

Stent Graft, Infrapopliteal, Venous Arterialization

Unknown
FDA source (opens on fda.gov)

QWN is the FDA product code for Stent Graft, Infrapopliteal, Venous Arterialization, a class III device type. FDA's definition for this code reads: "For performing percutaneous arterialization of the deep veins to restore blood flow in the lower limbs". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
QWN
Device name
Stent Graft, Infrapopliteal, Venous Arterialization
FDA definition
For performing percutaneous arterialization of the deep veins to restore blood flow in the lower limbs
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
Yes
Life sustaining or supporting
Yes
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