Cleared Traditional

K800944 - MEDTRONIC MODEL 69575

K800944 is the FDA 510(k) clearance for MEDTRONIC MODEL 69575 by Medtronic Vascular. It is a Class 3 Cardiovascular device (product code DTB) cleared through the Traditional 510(k) pathway after a 157-day FDA review.

K800944 · Medtronic Vascular · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 1980
Decision
157d
Days
Class 3
Risk

K800944 is an FDA 510(k) clearance for the MEDTRONIC MODEL 69575. 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 September 26, 1980 after a review of 157 days - an extended review cycle.

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 K800944 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 22, 1980
Decision Date September 26, 1980
Days to Decision 157 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
32d slower than avg
Panel avg: 125d · This submission: 157d
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 K800944.
PACEPATH MODEL 819
K801417 · Pacesetter Systems · Oct 1980
LEAD, ENDOCARDIAL, TINED, BIPOLAR, 5MM
K801455 · Pacesetter Systems · Oct 1980
IMPLANTABLE ENDOCARDIAL POROUS TIP ELEC.
K801792 · Telectronics, Inc. · Oct 1980
PERMANENT & TEMP. PACEMAKER ELECTRODE
K800795 · Daig Corp. · Jun 1980
LIFELINE TLE (TRAEBECULAR LODGING ELEC
K792300 · Intermedics, Inc. · Jun 1980
LIFELINE TLE J-SHAPED ATRIAL ENDOCARDIAL
K792301 · Intermedics, Inc. · Jun 1980