Cleared Traditional

K060873 - VANGUARD MRI AUXILIARY PATIENT TABLE WITH 4 AND 8 CHANNEL COIL ARRAY FOR GE SIGNA SYSTEMS (FDA 510(k) Clearance)

Class II Radiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K060873 · Sentinelle Medical, Inc. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 2006
Decision
15d
Days
Class 2
Risk

K060873 is an FDA 510(k) clearance for the VANGUARD MRI AUXILIARY PATIENT TABLE WITH 4 AND 8 CHANNEL COIL ARRAY FOR GE S.... Classified as Coil, Magnetic Resonance, Specialty (product code MOS), Class II - Special Controls.

Submitted by Sentinelle Medical, Inc. (Toronto, Ontario, CA). The FDA issued a Cleared decision on April 14, 2006 after a review of 15 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. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Sentinelle Medical, Inc. devices

Submission Details

510(k) Number K060873 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 30, 2006
Decision Date April 14, 2006
Days to Decision 15 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review Yes - reviewed by an FDA-accredited third party
Regulatory Context
Review time vs. panel average
92d faster than avg
Panel avg: 107d · This submission: 15d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

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 487
Devices cleared under the same product code (MOS) and FDA review panel - the closest regulatory comparables to K060873.
0.55T 12Ch Breast Coil
K260947 · Neocoil, LLC · Apr 2026
HD 8Ch Wrist Array
K252587 · Shenzhen RF Tech Co., Ltd. · Apr 2026
GEM Flex Coil 16-L Array, 3.0T Receive Only
K252876 · Shenzhen RF Tech Co., Ltd. · Apr 2026
Smart Fit TorsoCardiac 1.5T
K260519 · Philips Healthcare (Suzhou) Co., Ltd. · Mar 2026
GEM Flex Coil 16-L Array, 1.5T Receive Only
K252179 · Shenzhen RF Tech Co., Ltd. · Feb 2026
3.0T AIR 32CH HNA
K253738 · Ge Healthcare Coils (Usa Instruments, Inc.) · Jan 2026