Cleared Special

K140856 - BRACHYSOURCE SEED IMPLANTS WITH SOURCECAP BIOABSORBABLE CAPS

K140856 is an FDA 510(k) clearance for BRACHYSOURCE SEED IMPLANTS WITH SOURCEC..., manufactured by C.R. Bard, Inc.. The device is a Class 2 Radiology device with product code KXK cleared through the Special 510(k) pathway after a 29-day FDA review.

K140856 · C.R. Bard, Inc. · Radiology device
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May 2014
Decision
29d
Days
Class 2
Risk

K140856 is an FDA 510(k) clearance for the BRACHYSOURCE SEED IMPLANTS WITH SOURCECAP BIOABSORBABLE CAPS. Classified as Source, Brachytherapy, Radionuclide (product code KXK), Class II - Special Controls.

Submitted by C.R. Bard, Inc. (Covington, US). The FDA issued a Cleared decision on May 2, 2014 after a review of 29 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.5730 - the FDA radiology and imaging software oversight framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all C.R. Bard, Inc. devices

FDA 510(k) Submission Details - K140856

510(k) Number K140856 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 03, 2014
Decision Date May 02, 2014
Days to Decision 29 days
Submission Type Special
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
78d faster than avg
Panel avg: 107d · This submission: 29d
Pathway characteristics
Modification to existing cleared device.

KXK Device Classification - Class 2, Special Controls

Product Code KXK Source, Brachytherapy, Radionuclide
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.5730
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 - KXK Source, Brachytherapy, Radionuclide

All 97
Devices cleared under the same product code (KXK) and FDA review panel - the closest regulatory comparables to K140856.
ANT MODEL 1
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MRI MARKER
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