Cleared Traditional

K113008 - KODAMA INTRAVASCULAR ULRASOUND CATHETER

K113008 is an FDA 510(k) clearance for KODAMA INTRAVASCULAR ULRASOUND CATHETER, manufactured by Silicon Vally Medical Instruments, Inc.. The device is a Class 2 Cardiovascular device with product code OBJ cleared through the Traditional 510(k) pathway after a 251-day FDA review.

K113008 · Silicon Vally Medical Instruments, Inc. · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2012
Decision
251d
Days
Class 2
Risk

K113008 is an FDA 510(k) clearance for the KODAMA INTRAVASCULAR ULRASOUND CATHETER. Classified as Catheter, Ultrasound, Intravascular (product code OBJ), Class II - Special Controls.

Submitted by Silicon Vally Medical Instruments, Inc. (Fremont, US). The FDA issued a Cleared decision on June 14, 2012 after a review of 251 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1200 - the FDA cardiovascular device 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 Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Silicon Vally Medical Instruments, Inc. devices

FDA 510(k) Submission Details - K113008

510(k) Number K113008 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 07, 2011
Decision Date June 14, 2012
Days to Decision 251 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
126d slower than avg
Panel avg: 125d · This submission: 251d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

OBJ Device Classification - Class 2, Special Controls

Product Code OBJ Catheter, Ultrasound, Intravascular
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1200
Definition For Intracardiac And Intraluminal Visualization Of Cardiovascular Anatomy And Physiology.
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 Cardiovascular devices follow this clearance model.

Regulatory Peers - OBJ Catheter, Ultrasound, Intravascular

All 63
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