PMA supplement

P890003 S292: CARELINK HOME MONITOR,CARDIOSIGHT READER,CARELINK NETWORK DEVICE DATA MANAGEMENT APPLICATION

FDA PMA supplement · Normal 180 Day Track No User Fee · Medtronic, Inc.

Key facts

Original PMA P890003
Supplement number S292
Supplement type Normal 180 Day Track No User Fee
Reason for the supplement Postapproval Study Protocol - OSB
Trade name CARELINK HOME MONITOR,CARDIOSIGHT READER,CARELINK NETWORK DEVICE DATA MANAGEMENT APPLICATION
Generic name Pulse generator, permanent, implantable
Applicant Medtronic, Inc.
Product code NVZ
Received date Nov 12, 2013
Decision date Nov 22, 2013

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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