Cleared Traditional

K932769 - CAMINO VENTRICULAR DRAINAGE SYSTEM

K932769 is the FDA 510(k) clearance for CAMINO VENTRICULAR DRAINAGE SYSTEM by Camino Laboratories, Inc.. It is a Class 2 Neurology device (product code JXG) cleared through the Traditional 510(k) pathway after a 660-day FDA review.

K932769 · Camino Laboratories, Inc. · Neurology device
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Mar 1995
Decision
660d
Days
Class 2
Risk

K932769 is an FDA 510(k) clearance for the CAMINO VENTRICULAR DRAINAGE SYSTEM. Classified as Shunt, Central Nervous System And Components (product code JXG), Class II - Special Controls.

Submitted by Camino Laboratories, Inc. (San Diego, US). The FDA issued a Cleared decision on March 30, 1995 after a review of 660 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.5550 - the FDA neurology 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Neurology submissions.

View all Camino Laboratories, Inc. devices

Submission Details

510(k) Number K932769 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 08, 1993
Decision Date March 30, 1995
Days to Decision 660 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
512d slower than avg
Panel avg: 148d · This submission: 660d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JXG Shunt, Central Nervous System And Components
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.5550
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 Neurology devices follow this clearance model.

Regulatory Peers - JXG Shunt, Central Nervous System And Components

All 157
Devices cleared under the same product code (JXG) and FDA review panel - the closest regulatory comparables to K932769.
CORDIS HORIZONTAL-VERICAL VALVE SYSTEM
K944595 · Cordis Corp. · Oct 1995
PS MEDICAL BIOGLIDE CSF-FLOW CONTROL SHUNT KIT
K951258 · Pudenz-Schulte Medical Research Corp. · Sep 1995
CODMAN-MEDOS VALVE SHUNT SYSTEM
K944222 · Johnson & Johnson Professionals, Inc. · Jul 1995
CORDIS GRAVITY COMPENSATING ACCESSORY
K932429 · Cordis Corp. · Jul 1994
PS MEDICAL DELTA BURR HOLE VALVE
K934545 · Pudenz-Schulte Medical Research Corp. · Apr 1994
CORDIS POLYPROPYLENE BURR HOLE RESERVOIR
K925810 · Cordis Corp. · Mar 1994