Cleared Traditional

K925108 - INTEGRATED VISUALIZATION SYSTEM

K925108 is an FDA 510(k) clearance for INTEGRATED VISUALIZATION SYSTEM, manufactured by Neuro Navigational Corp.. The device is a Class 1 General & Plastic Surgery device with product code FWF cleared through the Traditional 510(k) pathway after a 112-day FDA review.

K925108 · Neuro Navigational Corp. · General & Plastic Surgery device
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Jan 1993
Decision
112d
Days
Class 1
Risk

K925108 is an FDA 510(k) clearance for the INTEGRATED VISUALIZATION SYSTEM. Classified as Camera, Television, Endoscopic, Without Audio (product code FWF), Class I - General Controls.

Submitted by Neuro Navigational Corp. (Costa Mesa, US). The FDA issued a Cleared decision on January 29, 1993 after a review of 112 days - within the typical 510(k) review window.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4160 - 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 Neuro Navigational Corp. devices

FDA 510(k) Submission Details - K925108

510(k) Number K925108 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 09, 1992
Decision Date January 29, 1993
Days to Decision 112 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
3d faster than avg
Panel avg: 115d · This submission: 112d
Pathway characteristics
Predicate-based equivalence.

FWF Device Classification - Class 1, General Controls

Product Code FWF Camera, Television, Endoscopic, Without Audio
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4160
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - FWF Camera, Television, Endoscopic, Without Audio

All 7
Devices cleared under the same product code (FWF) and FDA review panel - the closest regulatory comparables to K925108.
ENDOCAM CAMERA SYSTEMS 5502/5507 WITH CR CAMERA HEADS AND ACCESSORIES
K982965 · Richard Wolf Medical Instruments Corp. · Nov 1998
FUJINON VIDEO LAPAROSCOPE, MODIFIED
K930297 · Fujinon, Inc. · Mar 1994
VIDEO CAMERA W/ ELECTRONIC SHUTTER MODEL VCE-10
K930053 · Medical Devices, Inc. · May 1993
THE KARL STORZ MINI 9000 SOLID STATE CCD VIDEO CAM
K881014 · KARL STORZ Endoscopy-America, Inc. · Apr 1988
RGB CAMERA SYSTEM
K872661 · Aspen Laboratories, Inc. · Jul 1987
VIDEO CAMERA SYSTEM
K863598 · American Edwards Laboratories · Oct 1986