Cleared Traditional

K812580 - MEDTRONIC MODEL 2409

K812580 is the FDA 510(k) clearance for MEDTRONIC MODEL 2409 by Medtronic Vascular. It is a Class 3 Cardiovascular device (product code DXY) cleared through the Traditional 510(k) pathway after a 13-day FDA review.

K812580 · Medtronic Vascular · Cardiovascular device
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Sep 1981
Decision
13d
Days
Class 3
Risk

K812580 is an FDA 510(k) clearance for the MEDTRONIC MODEL 2409. Classified as Implantable Pacemaker Pulse-generator (product code DXY), Class III - Premarket Approval.

Submitted by Medtronic Vascular (Walker, US). The FDA issued a Cleared decision on September 23, 1981 after a review of 13 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.3610 - the FDA cardiovascular device oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: High-complexity regulatory submission. High regulatory complexity profile. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Medtronic Vascular devices

Submission Details

510(k) Number K812580 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 10, 1981
Decision Date September 23, 1981
Days to Decision 13 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
112d faster than avg
Panel avg: 125d · This submission: 13d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code DXY Implantable Pacemaker Pulse-generator
Device Class Class 3 - Premarket Approval
CFR Regulation 21 CFR 870.3610
What this classification means

Class III devices typically require Premarket Approval (PMA) with clinical evidence. Clearance through 510(k) for Class III devices is granted only when substantial equivalence to a valid predicate can be established.

Regulatory Peers - DXY Implantable Pacemaker Pulse-generator

All 338
Devices cleared under the same product code (DXY) and FDA review panel - the closest regulatory comparables to K812580.
KALOS-03
K812218 · Biotronik Sales, Inc. · Oct 1981
CYBERLITH IX IMPLANTABLE PULSE GENERATOR
K801337 · Intermedics, Inc. · Sep 1981
TELEMETRY DECODER
K801339 · Intermedics, Inc. · Sep 1981
MEDTRONIC ENERTRAX MODEL 7100
K812096 · Medtronic Vascular · Sep 1981
MEDTRONIC SPECTRAX
K812153 · Medtronic Vascular · Aug 1981
COMMAND P5(BIPOLAR PULSE GENERATOR)
K811402 · Cardiac Pacemakers, Inc. · Jul 1981