Cleared Traditional

K864618 - IMPLANTABLE ELECTRODE LEAD

K864618 is an FDA 510(k) clearance for IMPLANTABLE ELECTRODE LEAD, manufactured by Telectronics, Inc.. The device is a Class 3 Cardiovascular device with product code DTB cleared through the Traditional 510(k) pathway after a 178-day FDA review.

K864618 · Telectronics, Inc. · Cardiovascular device
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May 1987
Decision
178d
Days
Class 3
Risk

K864618 is an FDA 510(k) clearance for the IMPLANTABLE ELECTRODE LEAD, MODEL 030-439. Classified as Permanent Pacemaker Electrode (product code DTB), Class III - Premarket Approval.

Submitted by Telectronics, Inc. (Suffield, US). The FDA issued a Cleared decision on May 21, 1987 after a review of 178 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 Telectronics, Inc. devices

FDA 510(k) Submission Details - K864618

510(k) Number K864618 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 24, 1986
Decision Date May 21, 1987
Days to Decision 178 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
53d slower than avg
Panel avg: 125d · This submission: 178d
Pathway characteristics
Predicate-based equivalence.

DTB Device Classification - Class 3, Premarket Approval

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 387
Devices cleared under the same product code (DTB) and FDA review panel - the closest regulatory comparables to K864618.
PICF 0860/PSCF 0860/PSC 0860/PIAF 0860/PSAF 0860
K872731 · Ela Medical, Inc. · Sep 1987
SLIMLINE UNIPOLAR ENDOCARDIAL PACING LEAD, 030-438
K865098 · Telectronics, Inc. · Aug 1987
IMPLANTABLE PACING LEAD MODELS 487-06 TO 430-01
K871580 · Intermedics, Inc. · May 1987
ELECTRODE, PACEMAKER, PERMANENT & TEMPORARY
K870357 · Intermedics, Inc. · May 1987
MODEL 366-12 ADAPTAID (TM) STEP-DOWN ADAPTER
K871625 · Intermedics, Inc. · May 1987
IMPLANTABLE TINED, TRANS. PACING LEAD/REVIS. LABEL
K871333 · Medtronic Vascular · May 1987