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Assurant Cobalt Iliac Balloon-Expandable Stent System

by Medtronic, Ireland

PMA P110011

Withdrawn Withdrawn in United States.

Was authorized under PMA, withdrawn

Ended

Withdrawn 26 Oct 2011

PMA

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA PMA, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA PMAAPWD Approval withdrawn NumberP110011 Date26 Oct 2011Approval withdrawnStatusWithdrawn

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA PMA Withdrawn

Specification

PMA

Full name
Assurant Colbalt Iliac Ballon-Expandable Stent System
Trade Name
Assurant Cobalt Iliac Balloon-Expandable Stent System
Generic Name
STENT, ILIAC
PMA Number
FDA Product Code
NIO
Device Class
Class III
Advisory Committee
Cardiovascular
FDA Decision
APWD Approval withdrawn

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