Cleared Traditional

K040745 - MODIFIED CONCENTRIC RETRIEVER, MODEL 90038

K040745 is an FDA 510(k) clearance for MODIFIED CONCENTRIC RETRIEVER, manufactured by Concentric Medical, Inc.. The device is a Class 2 Cardiovascular device with product code DQY cleared through the Traditional 510(k) pathway after a 141-day FDA review.

K040745 · Concentric Medical, Inc. · Cardiovascular device
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Aug 2004
Decision
141d
Days
Class 2
Risk

K040745 is an FDA 510(k) clearance for the MODIFIED CONCENTRIC RETRIEVER, MODEL 90038. Classified as Catheter, Percutaneous (product code DQY), Class II - Special Controls.

Submitted by Concentric Medical, Inc. (Mountain View, US). The FDA issued a Cleared decision on August 11, 2004 after a review of 141 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1250 - 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.

View all Concentric Medical, Inc. devices

FDA 510(k) Submission Details - K040745

510(k) Number K040745 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 23, 2004
Decision Date August 11, 2004
Days to Decision 141 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
16d slower than avg
Panel avg: 125d · This submission: 141d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DQY Device Classification - Class 2, Special Controls

Product Code DQY Catheter, Percutaneous
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1250
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 - DQY Catheter, Percutaneous

All 781
Devices cleared under the same product code (DQY) and FDA review panel - the closest regulatory comparables to K040745.
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KERBEROS OCCLUDING GUIDE CATHETER AND ACCESSORIES
K041151 · Kerberos Proximal Solutions, Inc. · Jul 2004
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K040700 · Concentric Medical, Inc. · Jun 2004
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K033540 · Medtronic Vascular · May 2004