Cleared Special

K000274 - EOPA ELONGATED ONE-PIECE ARTERIAL CANNULA WITH GUIDEWIRE

K000274 is an FDA 510(k) clearance for EOPA ELONGATED ONE-PIECE ARTERIAL CANNU..., manufactured by Medtronic Cardiac Surgical Products. The device is a Class 2 Cardiovascular device with product code DWF cleared through the Special 510(k) pathway after a 10-day FDA review.

K000274 · Medtronic Cardiac Surgical Products · Cardiovascular device
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Optimized for regulatory review, auditing and printing
Feb 2000
Decision
10d
Days
Class 2
Risk

K000274 is an FDA 510(k) clearance for the EOPA ELONGATED ONE-PIECE ARTERIAL CANNULA WITH GUIDEWIRE. Classified as Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass (product code DWF), Class II - Special Controls.

Submitted by Medtronic Cardiac Surgical Products (Grand Rapids, US). The FDA issued a Cleared decision on February 10, 2000 after a review of 10 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4210 - 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 Cardiac Surgical Products devices

FDA 510(k) Submission Details - K000274

510(k) Number K000274 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 31, 2000
Decision Date February 10, 2000
Days to Decision 10 days
Submission Type Special
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
115d faster than avg
Panel avg: 125d · This submission: 10d
Pathway characteristics
Modification to existing cleared device.

DWF Device Classification - Class 2, Special Controls

Product Code DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4210
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 - DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

All 331
Devices cleared under the same product code (DWF) and FDA review panel - the closest regulatory comparables to K000274.
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T-ANASTAFLO
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