Maxim PFS Model 033-301 Pacing Lead

by St. Jude Medical, Cardiac Rhythm Management Divisi

PMA P920011

Withdrawn Withdrawn in United States.

Was authorized under PMA

Ended

Withdrawn 7 Nov 1996

PMA

FDA recalls

in data synced 22 Oct 2026

Documents

was PMA P920011↗

FDA record

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

Region	Authorization	Number	Date	Status
United States	FDA PMAAPWD Approval withdrawn	NumberP920011	Date7 Nov 1996Approval withdrawn	StatusWithdrawn

Recalls

0 recalls · FDA

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

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA PMA Withdrawn

Specification

PMA

Full name: Maxim Pfs Model 033-301

Generic Name: permanent pacemaker Electrode

PMA Number: P920011
FDA Product Code: DTB

Device Class: Class III
Regulation: 21 CFR Part 870.3680
Advisory Committee: Cardiovascular
FDA Decision: APWD Approval withdrawn

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