Cleared Special

K151110 - Intersept Filtered Cardiotomy Reservoir

K151110 is an FDA 510(k) clearance for Intersept Filtered Cardiotomy Reservoir, manufactured by Medtronic, Inc.. The device is a Class 2 Cardiovascular device with product code DTN cleared through the Special 510(k) pathway after a 30-day FDA review.

K151110 · Medtronic, Inc. · Cardiovascular device
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May 2015
Decision
30d
Days
Class 2
Risk

K151110 is an FDA 510(k) clearance for the Intersept Filtered Cardiotomy Reservoir. Classified as Reservoir, Blood, Cardiopulmonary Bypass (product code DTN), Class II - Special Controls.

Submitted by Medtronic, Inc. (Minneapolis, US). The FDA issued a Cleared decision on May 27, 2015 after a review of 30 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4400 - the FDA cardiovascular device oversight framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Medtronic, Inc. devices

FDA 510(k) Submission Details - K151110

510(k) Number K151110 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 27, 2015
Decision Date May 27, 2015
Days to Decision 30 days
Submission Type Special
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
95d faster than avg
Panel avg: 125d · This submission: 30d
Pathway characteristics
Modification to existing cleared device.

DTN Device Classification - Class 2, Special Controls

Product Code DTN Reservoir, Blood, Cardiopulmonary Bypass
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4400
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 - DTN Reservoir, Blood, Cardiopulmonary Bypass

All 140
Devices cleared under the same product code (DTN) and FDA review panel - the closest regulatory comparables to K151110.
Intersept Filtered Cardiotomy Reservoir with Cortiva BioActive Surface
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