Cleared Traditional

K801038 - ADAPTAID ELEMA LEAD ADAPTER KIT 365-17

K801038 is an FDA 510(k) clearance for ADAPTAID ELEMA LEAD ADAPTER KIT 365-17, manufactured by Intermedics, Inc.. The device is a Class 2 Cardiovascular device with product code DTD cleared through the Traditional 510(k) pathway after a 67-day FDA review.

K801038 · Intermedics, Inc. · Cardiovascular device
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Jul 1980
Decision
67d
Days
Class 2
Risk

K801038 is an FDA 510(k) clearance for the ADAPTAID ELEMA LEAD ADAPTER KIT 365-17. Classified as Pacemaker Lead Adaptor (product code DTD), Class II - Special Controls.

Submitted by Intermedics, Inc. (Mchenry, US). The FDA issued a Cleared decision on July 8, 1980 after a review of 67 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.3620 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Intermedics, Inc. devices

FDA 510(k) Submission Details - K801038

510(k) Number K801038 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 02, 1980
Decision Date July 08, 1980
Days to Decision 67 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
58d faster than avg
Panel avg: 125d · This submission: 67d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DTD Device Classification - Class 2, Special Controls

Product Code DTD Pacemaker Lead Adaptor
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.3620
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Peers - DTD Pacemaker Lead Adaptor

All 86
Devices cleared under the same product code (DTD) and FDA review panel - the closest regulatory comparables to K801038.
PACEMAKER LEAD ADAPTOR MODEL 431
K802407 · Pacesetter Systems · Oct 1980
UNIPOLAR TO BIPOLAR PULSE GEN. ADAPTER
K802077 · Cardiac Pacemakers, Inc. · Oct 1980
ADAPTAID HELICAL COIL ADAPTER 365-14
K801039 · Intermedics, Inc. · Jul 1980
GE LEAD ADAPTER, MODEL 345-01
K801040 · Intermedics, Inc. · Jun 1980
ADAPTER KIT
K800353 · Daig Corp. · May 1980
BIPOLAR LEAD ADAPTOR, MODEL BA-415
K790218 · Pacesetter Systems · Aug 1979