Cleared Traditional

K123571 - CARDIO VISION MICS AORTIC CLAMPS

K123571 is an FDA 510(k) clearance for CARDIO VISION MICS AORTIC CLAMPS, manufactured by Cardiomedical GmbH. The device is a Class 2 Cardiovascular device with product code DXC cleared through the Traditional 510(k) pathway after a 254-day FDA review.

K123571 · Cardiomedical GmbH · Cardiovascular device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Aug 2013
Decision
254d
Days
Class 2
Risk

K123571 is an FDA 510(k) clearance for the CARDIO VISION MICS AORTIC CLAMPS. Classified as Clamp, Vascular (product code DXC), Class II - Special Controls.

Submitted by Cardiomedical GmbH (Amsterdam, NL). The FDA issued a Cleared decision on August 1, 2013 after a review of 254 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4450 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K123571

510(k) Number K123571 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 20, 2012
Decision Date August 01, 2013
Days to Decision 254 days
Submission Type Traditional
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
129d slower than avg
Panel avg: 125d · This submission: 254d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DXC Device Classification - Class 2, Special Controls

Product Code DXC Clamp, Vascular
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4450
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 - DXC Clamp, Vascular

All 193
Devices cleared under the same product code (DXC) and FDA review panel - the closest regulatory comparables to K123571.
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K123571 · CARDIO VISION MICS AORTIC CLAMPS
Download PDF FDA Summary Cardiomedical GmbH