Cleared Traditional

K090417 - AXXENT FLEXISHIELD MINI

K090417 is an FDA 510(k) clearance for AXXENT FLEXISHIELD MINI, manufactured by Xoft, Inc.. The device is a Class 2 Radiology device with product code IXI cleared through the Traditional 510(k) pathway after a 125-day FDA review.

K090417 · Xoft, Inc. · Radiology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Jun 2009
Decision
125d
Days
Class 2
Risk

K090417 is an FDA 510(k) clearance for the AXXENT FLEXISHIELD MINI. Classified as Block, Beam-shaping, Radiation Therapy (product code IXI), Class II - Special Controls.

Submitted by Xoft, Inc. (Sunnyvale, US). The FDA issued a Cleared decision on June 23, 2009 after a review of 125 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.5710 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K090417

510(k) Number K090417 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 18, 2009
Decision Date June 23, 2009
Days to Decision 125 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
18d slower than avg
Panel avg: 107d · This submission: 125d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IXI Device Classification - Class 2, Special Controls

Product Code IXI Block, Beam-shaping, Radiation Therapy
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.5710
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 - IXI Block, Beam-shaping, Radiation Therapy

All 48
Devices cleared under the same product code (IXI) and FDA review panel - the closest regulatory comparables to K090417.
.DECIMAL ELECTRON APERTURE
K111759 · .Decimal, Inc. · Sep 2011
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K091403 · Oncology Tech, LLC · Jul 2009
BOLUS COMPENSATOR
K091911 · .Decimal, Inc. · Jul 2009
.DECIMAL RANGE COMPENSATOR
K071078 · .Decimal, Inc. · May 2007
.DECIMAL APERTURE
K071077 · .Decimal, Inc. · May 2007
MOD1 COMPENSATORS FOR RADIATION BEAM THERAPY
K062781 · Symtium Corporation · Nov 2006
K090417 · AXXENT FLEXISHIELD MINI
Download PDF FDA Summary Xoft, Inc.