Cleared Traditional

K862513 - EXTERNAL VENTRICULAR & LUMBAR DRAINAGE SETS

K862513 is an FDA 510(k) clearance for EXTERNAL VENTRICULAR & LUMBAR DRAINAGE SETS, manufactured by Cordis Corp.. The device is a Class 2 Neurology device with product code JXG cleared through the Traditional 510(k) pathway after a 31-day FDA review.

K862513 · Cordis Corp. · Neurology device
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Aug 1986
Decision
31d
Days
Class 2
Risk

K862513 is an FDA 510(k) clearance for the EXTERNAL VENTRICULAR & LUMBAR DRAINAGE SETS. Classified as Shunt, Central Nervous System And Components (product code JXG), Class II - Special Controls.

Submitted by Cordis Corp. (Miami, US). The FDA issued a Cleared decision on August 1, 1986 after a review of 31 days - a notably fast clearance 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: 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 Cordis Corp. devices

FDA 510(k) Submission Details - K862513

510(k) Number K862513 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 01, 1986
Decision Date August 01, 1986
Days to Decision 31 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
117d faster than avg
Panel avg: 148d · This submission: 31d
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 177
Devices cleared under the same product code (JXG) and FDA review panel - the closest regulatory comparables to K862513.
HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEM
K864676 · American V. Mueller · Dec 1986
P-S MEDICAL CSF-SIPHON CONTROL DEVICE
K862907 · Pudenz-Schulte Medical Research Corp. · Dec 1986
BECKER EXTERNAL DRAINAGE/MONITOR SYS LUMBAR CATH.
K862303 · Pudenz-Schulte Medical Research Corp. · Aug 1986
STANDARD/PEDIATRIC CORDIS HYDROCEPHALUS VALVES
K861377 · Cordis Corp. · Jun 1986
EVDS, EVMDS, LDS & IVMCS CENTRAL NERVOUS SYS FLUID
K855058 · Cordis Corp. · Jan 1986
HEYER-SCHULTE SYRINGO PERITONEAL SHUNT
K854049 · American V. Mueller · Nov 1985