Cleared Traditional

K964923 - CODMAN LUMBAR DRAINAGE CATHETER KIT

K964923 is an FDA 510(k) clearance for CODMAN LUMBAR DRAINAGE CATHETER KIT, manufactured by Johnson & Johnson Professionals, Inc.. The device is a Class 2 Neurology device with product code JXG cleared through the Traditional 510(k) pathway after a 198-day FDA review.

K964923 · Johnson & Johnson Professionals, Inc. · Neurology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 1997
Decision
198d
Days
Class 2
Risk

K964923 is an FDA 510(k) clearance for the CODMAN LUMBAR DRAINAGE CATHETER KIT. Classified as Shunt, Central Nervous System And Components (product code JXG), Class II - Special Controls.

Submitted by Johnson & Johnson Professionals, Inc. (Raynham, US). The FDA issued a Cleared decision on June 25, 1997 after a review of 198 days - an extended review cycle.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Neurology review framework, consistent with the majority of Class II 510(k) submissions.

View all Johnson & Johnson Professionals, Inc. devices

FDA 510(k) Submission Details - K964923

510(k) Number K964923 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 09, 1996
Decision Date June 25, 1997
Days to Decision 198 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
50d slower than avg
Panel avg: 148d · This submission: 198d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JXG Device Classification - Class 2, Special Controls

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 225
Devices cleared under the same product code (JXG) and FDA review panel - the closest regulatory comparables to K964923.
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RADIONICS CONTOUR FLEX VALVE, RADIONICS CONTOUR FLEX PLUS VALVE
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PERITONEAL/CARDIAC CATHETER
K970983 · Integra Neurocare, LLC · Jun 1997
RADIONICS BURR HOLE VALVE
K970578 · Radionics, Inc. · Jun 1997
LUMBAR DRAINAGE ACCESSORY KIT
K970658 · Integra Neurocare, LLC · May 1997