Cleared Traditional

K992006 - NEUROVIEW INSTRUMENT HOLDER

K992006 is an FDA 510(k) clearance for NEUROVIEW INSTRUMENT HOLDER, manufactured by Integra Neurocare, LLC. The device is a Class 2 Gastroenterology & Urology device with product code OCV cleared through the Traditional 510(k) pathway after a 63-day FDA review.

K992006 · Integra Neurocare, LLC · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 1999
Decision
63d
Days
Class 2
Risk

K992006 is an FDA 510(k) clearance for the NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33. Classified as Endoscope Holder (product code OCV), Class II - Special Controls.

Submitted by Integra Neurocare, LLC (San Diego, US). The FDA issued a Cleared decision on August 17, 1999 after a review of 63 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1500 - the FDA gastroenterology and urology 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Integra Neurocare, LLC devices

FDA 510(k) Submission Details - K992006

510(k) Number K992006 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 15, 1999
Decision Date August 17, 1999
Days to Decision 63 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
67d faster than avg
Panel avg: 130d · This submission: 63d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

OCV Device Classification - Class 2, Special Controls

Product Code OCV Endoscope Holder
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1500
Definition To Hold Endoscope In A Desired Position During Procedures.
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 Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - OCV Endoscope Holder

Devices cleared under the same product code (OCV) and FDA review panel - the closest regulatory comparables to K992006.
KARL STORZ Holders
K240506 · KARL STORZ Endoscopy-America, Inc. · Oct 2024
ENDOFIX EXO
K232405 · Aktormed GmbH · Apr 2024
WalterLorenz Surgical Assist Arm Scope Holder
K190576 · Biomet Microfixation · Jun 2019
KSEA ENDOSCOPE HOLDER
K990334 · KARL STORZ Endoscopy-America, Inc. · Mar 1999
SH-1 SURGICAL HOLDER FOR TELESCOPE
K960068 · Olympus America, Inc. · May 1997