Cleared Traditional

K780623 - ENDOCARDIAL ATRIAL PACING LEAD

K780623 is the FDA 510(k) clearance for ENDOCARDIAL ATRIAL PACING LEAD by Medtronic Vascular. It is a Class 3 Cardiovascular device (product code DTB) cleared through the Traditional 510(k) pathway after a 105-day FDA review.

K780623 · Medtronic Vascular · Cardiovascular device
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Jul 1978
Decision
105d
Days
Class 3
Risk

K780623 is an FDA 510(k) clearance for the ENDOCARDIAL ATRIAL PACING LEAD, M. 6994. Classified as Permanent Pacemaker Electrode (product code DTB), Class III - Premarket Approval.

Submitted by Medtronic Vascular (Walker, US). The FDA issued a Cleared decision on July 28, 1978 after a review of 105 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.3680 - 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 K780623 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 14, 1978
Decision Date July 28, 1978
Days to Decision 105 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
20d faster than avg
Panel avg: 125d · This submission: 105d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code DTB Permanent Pacemaker Electrode
Device Class Class 3 - Premarket Approval
CFR Regulation 21 CFR 870.3680
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 - DTB Permanent Pacemaker Electrode

All 364
Devices cleared under the same product code (DTB) and FDA review panel - the closest regulatory comparables to K780623.
PACING LEADS MODEL UL-811 AND UL-813
K781776 · Pacesetter Systems · Oct 1978
PACEMAKER, ELECTRODE, PERMANENT & TEMP.
K780246 · Daig Corp. · Aug 1978
BIPOLAR ENDOCARDIAL PACING LEAD, M. 6902
K780622 · Medtronic Vascular · Jul 1978
LEAD, PACING, ATRIAL, ENDOCARDIAL, TINED
K780621 · Medtronic Vascular · Jul 1978
SUTURELESS MYOCARDIAL PACING LEAD
K780446 · Medtronic Vascular · May 1978
PACEMAKER, PERM. & TEMP., ELECTRODE
K772197 · Daig Corp. · Jan 1978