Cleared Traditional

K141785 - MICRO THERMX MICROWAVE ABLATION SYSTEM AND ACCESSORIES

K141785 is an FDA 510(k) clearance for MICRO THERMX MICROWAVE ABLATION SYSTEM ..., manufactured by Bsd Medical Corp.. The device is a Class 2 General & Plastic Surgery device with product code NEY cleared through the Traditional 510(k) pathway after a 272-day FDA review.

K141785 · Bsd Medical Corp. · General & Plastic Surgery device
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Mar 2015
Decision
272d
Days
Class 2
Risk

K141785 is an FDA 510(k) clearance for the MICRO THERMX MICROWAVE ABLATION SYSTEM AND ACCESSORIES. Classified as System, Ablation, Microwave And Accessories (product code NEY), Class II - Special Controls.

Submitted by Bsd Medical Corp. (Salt Lake City, US). The FDA issued a Cleared decision on March 31, 2015 after a review of 272 days - an extended review cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4400 - the FDA general and plastic surgery device 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 General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Bsd Medical Corp. devices

FDA 510(k) Submission Details - K141785

510(k) Number K141785 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 02, 2014
Decision Date March 31, 2015
Days to Decision 272 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
157d slower than avg
Panel avg: 115d · This submission: 272d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

NEY Device Classification - Class 2, Special Controls

Product Code NEY System, Ablation, Microwave And Accessories
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4400
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 General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - NEY System, Ablation, Microwave And Accessories

All 64
Devices cleared under the same product code (NEY) and FDA review panel - the closest regulatory comparables to K141785.
miraDry System
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K143203 · Medwaves Incorporated · Aug 2015
EMPRINT ABLATION SYSTEM
K133821 · Covidien, LLC · Apr 2014
CERTUS 140 CERTUSURGGT SURGICAL TOOL
K130399 · Neuwave Medical, Inc. · Jul 2013
CERTUS 140 2.45GHZ ABLATION SYSTEM
K122217 · Neuwave Medical, Inc. · Dec 2012