Cleared Special

K101833 - INFISTITCH FOR I5 DIGITAL X-RAY IMAGING SYSTEM, MODEL I5

K101833 is an FDA 510(k) clearance for INFISTITCH FOR I5 DIGITAL X-RAY IMAGING..., manufactured by Infimed, Inc.. The device is a Class 2 Radiology device with product code OWB cleared through the Special 510(k) pathway after a 22-day FDA review.

K101833 · Infimed, Inc. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2010
Decision
22d
Days
Class 2
Risk

K101833 is an FDA 510(k) clearance for the INFISTITCH FOR I5 DIGITAL X-RAY IMAGING SYSTEM, MODEL I5. Classified as Interventional Fluoroscopic X-ray System (product code OWB), Class II - Special Controls.

Submitted by Infimed, Inc. (Great Neck, US). The FDA issued a Cleared decision on July 23, 2010 after a review of 22 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1650 - 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 Infimed, Inc. devices

FDA 510(k) Submission Details - K101833

510(k) Number K101833 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 01, 2010
Decision Date July 23, 2010
Days to Decision 22 days
Submission Type Special
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
85d faster than avg
Panel avg: 107d · This submission: 22d
Pathway characteristics
Modification to existing cleared device.

OWB Device Classification - Class 2, Special Controls

Product Code OWB Interventional Fluoroscopic X-ray System
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1650
Definition Interventional Fluoroscopy
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 - OWB Interventional Fluoroscopic X-ray System

All 254
Devices cleared under the same product code (OWB) and FDA review panel - the closest regulatory comparables to K101833.
SYNGO AORTIC VALVEGUIDE SOFTWARE
K113027 · Siemens Medical Solutions USA, Inc. · Nov 2011
INFINIX-I INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000V
K101868 · Toshiba America Medical Systems, In.C · Sep 2010
ALLURA XPER OR TABLE SERIES
K102005 · Philips Medical Systems North America, Inc. · Aug 2010
ZEN-2090 PRO, FLUOROSCOPIC X-RAY SYSTEM, MODEL ZEN-2090 PRO
K091918 · Genoray Co., Ltd. · Oct 2009
GE INNOVA SOLID STATE XRAY-IMAGER FLUOROSCOPIC X-RAY SYSTEM, MODEL: 4100IQ, 3100IQ, 2100IQ
K092004 · Ge Healthcare · Aug 2009
GE INNOVA SOLID STATE XRAY-IMAGER FLUOROSCOPIC X-RAY SYSTEM, MODELS INNOVA 4100, 3100, 2100, 3131, 2121
K091658 · Ge Healthcare · Jun 2009