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

Stent Graft, Bypass, Superficial Femoral Artery

Unknown
FDA source (opens on fda.gov)

QWM is the FDA product code for Stent Graft, Bypass, Superficial Femoral Artery, a class III device type. FDA's definition for this code reads: "For bypassing stenosis in the superficial femoral artery via the femoral vein". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
QWM
Device name
Stent Graft, Bypass, Superficial Femoral Artery
FDA definition
For bypassing stenosis in the superficial femoral artery via the femoral vein
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