Cleared Traditional

MODEL 432-01 BIOPORE IMPLANTABLE PACING LEAD (K862053) - FDA 510(k) Clearance

Class III device cleared through the 510(k) pathway via substantial equivalence to a legally marketed predicate.

K862053 · Intermedics, Inc. · Cardiovascular device
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Sep 1986
Decision
113d
Days
Class 3
Risk

K862053 is an FDA 510(k) clearance for the MODEL 432-01 BIOPORE IMPLANTABLE PACING LEAD. Classified as Permanent Pacemaker Electrode (product code DTB), Class III - Premarket Approval.

Submitted by Intermedics, Inc. (Freeport, US). The FDA issued a Cleared decision on September 19, 1986 after a review of 113 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 Intermedics, Inc. devices

Submission Details

510(k) Number K862053 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 29, 1986
Decision Date September 19, 1986
Days to Decision 113 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
12d faster than avg
Panel avg: 125d · This submission: 113d
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 221
Devices cleared under the same product code (DTB) and FDA review panel - the closest regulatory comparables to K862053.
MODEL 493-08 POLYFLEX ENDOCARDIAL LEAD
K863781 · Intermedics, Inc. · Nov 1986
MODEL 366-28 ADAPTAID(TM) STEP-DOWN ADAPTER
K864047 · Intermedics, Inc. · Nov 1986
MODEL 366-27 ADAPTAID(TM) STEP-DOWN ADAPTER
K864048 · Intermedics, Inc. · Nov 1986
MODEL 430-01 BIOPORE IMPLANTABLE PACING LEAD
K862054 · Intermedics, Inc. · Sep 1986
CORDIS ANCOR ACTIVE FIXATION LEAD
K832422 · Cordis Corp. · Aug 1986
CORDIS HI-FLEX PERVENOUS ACTIVE FIXATION UNIPOLAR
K851064 · Cordis Corp. · Aug 1986