PMA supplement

P020025 S132: IntellaTip MiFi Filter Module, IntellaTip MiFi Reference Cable, EGM Cable, Maestro 4000 Footswitch

FDA PMA supplement · Real-Time Process · Boston Scientific

Key facts

Original PMA P020025
Supplement number S132
Supplement type Real-Time Process
Reason for the supplement Labeling Change - Indications/instructions/shelf life/tradename
Trade name IntellaTip MiFi Filter Module, IntellaTip MiFi Reference Cable, EGM Cable, Maestro 4000 Footswitch
Generic name Catheter, percutaneous, cardiac ablation, for treatment of atrial flutter
Applicant Boston Scientific
Product code OAD
Received date May 19, 2021
Decision date Aug 17, 2021

At a glance

  • No Expedited review granted
  • No Approval order on file
  • No Summary of safety and effectiveness on file

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About PMA supplements

A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.

Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date:

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