Cleared Traditional

K122217 - CERTUS 140 2.45GHZ ABLATION SYSTEM

K122217 is an FDA 510(k) clearance for CERTUS 140 2.45GHZ ABLATION SYSTEM, manufactured by Neuwave Medical, Inc.. The device is a Class 2 General & Plastic Surgery device with product code NEY cleared through the Traditional 510(k) pathway after a 147-day FDA review.

K122217 · Neuwave Medical, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 2012
Decision
147d
Days
Class 2
Risk

K122217 is an FDA 510(k) clearance for the CERTUS 140 2.45GHZ ABLATION SYSTEM. Classified as System, Ablation, Microwave And Accessories (product code NEY), Class II - Special Controls.

Submitted by Neuwave Medical, Inc. (Madision, US). The FDA issued a Cleared decision on December 19, 2012 after a review of 147 days - within the typical 510(k) review window.

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 Neuwave Medical, Inc. devices

FDA 510(k) Submission Details - K122217

510(k) Number K122217 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 25, 2012
Decision Date December 19, 2012
Days to Decision 147 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
32d slower than avg
Panel avg: 115d · This submission: 147d
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 67
Devices cleared under the same product code (NEY) and FDA review panel - the closest regulatory comparables to K122217.
MICRO THERMX MICROWAVE ABLATION SYSTEM AND ACCESSORIES
K141785 · Bsd Medical Corp. · Mar 2015
EMPRINT ABLATION SYSTEM
K133821 · Covidien, LLC · Apr 2014
CERTUS 140 CERTUSURGGT SURGICAL TOOL
K130399 · Neuwave Medical, Inc. · Jul 2013
ACCULIS ACCU21 PMTA MICROWAVE TISSUE ABLATION APPLICATOR
K122762 · Microsulis Medical Limited · Nov 2012
CERTUS 140 2.45GHZ ABLATION SYSTEM
K113237 · Neuwave Medical, Inc. · Jan 2012
CERTUS 140 MICROWAVE ABLATION SYSTEM AND ACCESSORIES, MODEL CERTUS 140
K100744 · Neuwave Medical, Inc. · Oct 2010