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

Aortic Stent

Unknown
FDA source (opens on fda.gov)

PNF is the FDA product code for Aortic Stent, a class III device type. FDA's definition for this code reads: "Coarctation of the Aorta". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
PNF
Device name
Aortic Stent
FDA definition
Coarctation of the Aorta
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