510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
NIPClass III

Stent, Superficial Femoral Artery

Unknown
FDA source (opens on fda.gov)

NIP is the FDA product code for Stent, Superficial Femoral Artery, a class III device type. FDA's definition for this code reads: "Stent, Superficial Femoral Artery -- a metal scaffold placed via a delivery catheter into the superficial femoral artery artery to maintain the lumen". As of , FDA records hold no 510(k) clearances under this code and 86 recalls.

Classification record

Product code
NIP
Device name
Stent, Superficial Femoral Artery
FDA definition
Stent, Superficial Femoral Artery -- a metal scaffold placed via a delivery catheter into the superficial femoral artery artery to maintain the lumen
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
86

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 31 companies shown, in name order