Cleared Special

K021575 - OBC-127 BREAST ARRAY COIL

K021575 is the FDA 510(k) clearance for OBC-127 BREAST ARRAY COIL by Mri Devices Corp.. It is a Class 2 Radiology device (product code MOS) cleared through the Special 510(k) pathway after a 29-day FDA review.

K021575 · Mri Devices Corp. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2002
Decision
29d
Days
Class 2
Risk

K021575 is an FDA 510(k) clearance for the OBC-127 BREAST ARRAY COIL. Classified as Coil, Magnetic Resonance, Specialty (product code MOS), Class II - Special Controls.

Submitted by Mri Devices Corp. (Waukesha, US). The FDA issued a Cleared decision on June 12, 2002 after a review of 29 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1000 - the FDA radiology and imaging software 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 Mri Devices Corp. devices

Submission Details

510(k) Number K021575 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 14, 2002
Decision Date June 12, 2002
Days to Decision 29 days
Submission Type Special
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
78d faster than avg
Panel avg: 107d · This submission: 29d
Pathway characteristics
Modification to existing cleared device.

Device Classification

Product Code MOS Coil, Magnetic Resonance, Specialty
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1000
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 Radiology devices follow this clearance model.

Regulatory Peers - MOS Coil, Magnetic Resonance, Specialty

All 311
Devices cleared under the same product code (MOS) and FDA review panel - the closest regulatory comparables to K021575.
MILLENNIUM 5000 MEUROVASCULAR COIL
K021141 · Usa Instruments, Inc. · Jun 2002
MODEL 415PH-64/42: PHASED ARRAY SHOULDER COIL
K021433 · Medical Advances, Inc. · Jun 2002
HNC-127-TRIO NEUROVASCULAR ARRAY COIL
K021570 · Mri Devices Corp. · Jun 2002
GPF-29 GENERAL PURPOSE COIL SET
K020850 · Mri Devices Corp. · Jun 2002
MAGNETOM SYMPHONY QUADRATURE TX/RX HEAD COIL
K021262 · Usa Instruments, Inc. · May 2002
NVA-63-8 NEUROVASCULAR ARRAY COIL
K020606 · Mri Devices Corp. · Mar 2002