Cleared Traditional

K051423 - MICK HDR INTERSTITIAL IMPLANT ACCESSORIES

K051423 is an FDA 510(k) clearance for MICK HDR INTERSTITIAL IMPLANT ACCESSORIES, manufactured by Mick Radio-Nuclear Instruments, Inc.. The device is a Class 2 Radiology device width product code JAQ cleared through the Traditional 510(k) pathway after a 30-day FDA review.

K051423 · Mick Radio-Nuclear Instruments, Inc. · Radiology device
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Jul 2005
Decision
30d
Days
Class 2
Risk

K051423 is an FDA 510(k) clearance for the MICK HDR INTERSTITIAL IMPLANT ACCESSORIES. Classified as System, Applicator, Radionuclide, Remote-controlled (product code JAQ), Class II - Special Controls.

Submitted by Mick Radio-Nuclear Instruments, Inc. (Mt. Vernon, US). The FDA issued a Cleared decision on July 1, 2005 after a review of 30 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.5700 - 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 Mick Radio-Nuclear Instruments, Inc. devices

Submission Details

510(k) Number K051423 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 01, 2005
Decision Date July 01, 2005
Days to Decision 30 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
77d faster than avg
Panel avg: 107d · This submission: 30d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JAQ System, Applicator, Radionuclide, Remote-controlled
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.5700
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 - JAQ System, Applicator, Radionuclide, Remote-controlled

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