Cleared Traditional

MODEL 438-03 CARDIFIX SIDE HOOK IMPLANT. PACE LEAD (K875100) - FDA 510(k) Clearance

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

K875100 · Intermedics, Inc. · Cardiovascular device
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May 1988
Decision
166d
Days
Class 3
Risk

K875100 is an FDA 510(k) clearance for the MODEL 438-03 CARDIFIX SIDE HOOK IMPLANT. PACE 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 May 24, 1988 after a review of 166 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 Intermedics, Inc. devices

Submission Details

510(k) Number K875100 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 10, 1987
Decision Date May 24, 1988
Days to Decision 166 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
41d slower than avg
Panel avg: 125d · This submission: 166d
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 K875100.
IMPLANTABLE ELECTRODE LEAD, MODEL 030-446
K874664 · Telectronics, Inc. · May 1988
MODEL 435-04 CARDIFIX SIDE HOOK IMPLANT. PACE LEAD
K875178 · Intermedics, Inc. · May 1988
MEDTRONIC MODEL 5866-36 LEAD ADAPTOR KIT
K881712 · Medtronic Vascular · May 1988
MODEL 438-02 CARDIFIX SIDE HOOK IMPLANT. PACE LEAD
K872126 · Intermedics, Inc. · Mar 1988
MODEL 439-07 AND 439-09 LIFELINE MYOCARDIAL LEAD
K880551 · Intermedics, Inc. · Mar 1988
MEDTRONIC MODEL 4016A ENDOCARDIAL PACING LEAD
K873962 · Medtronic Vascular · Feb 1988