Cleared Traditional

K936099 - NEUROLOGICAL LEAD ACCESSORIES

K936099 is the FDA 510(k) clearance for NEUROLOGICAL LEAD ACCESSORIES by Medtronic Vascular. It is a Class 2 Neurology device (product code GZB) cleared through the Traditional 510(k) pathway after a 201-day FDA review.

K936099 · Medtronic Vascular · Neurology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 1994
Decision
201d
Days
Class 2
Risk

K936099 is an FDA 510(k) clearance for the NEUROLOGICAL LEAD ACCESSORIES. Classified as Stimulator, Spinal-cord, Implanted (pain Relief) (product code GZB), Class II - Special Controls.

Submitted by Medtronic Vascular (Minneapolis, US). The FDA issued a Cleared decision on July 11, 1994 after a review of 201 days - an extended review cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.5880 - 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 Medtronic Vascular devices

Submission Details

510(k) Number K936099 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 22, 1993
Decision Date July 11, 1994
Days to Decision 201 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
53d slower than avg
Panel avg: 148d · This submission: 201d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GZB Stimulator, Spinal-cord, Implanted (pain Relief)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.5880
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 - GZB Stimulator, Spinal-cord, Implanted (pain Relief)

All 74
Devices cleared under the same product code (GZB) and FDA review panel - the closest regulatory comparables to K936099.
ALTERNATE 100% ETO STERILIZATION PROCESS AND ALTERNATE STERILIZATION FACCILITY
K950127 · Medtronic Vascular · Jan 1995
TEMP AND PERMANENT NEURO LEADS (VARIOUS MODELS)
K945103 · Medtronic Vascular · Jan 1995
NEUROLOGICAL LEADS (PACKAGING MODIFICATION)
K940416 · Medtronic Vascular · Jul 1994
TEMPORARY SCREENING LEAD/CATHETER KIT
K934938 · Medtronic Vascular · Jun 1994
MODEL 3862A & B 3863A & B TEMP. LEAD SCREENING KIT
K932202 · Medtronic Vascular · May 1994
MEDTRONIC MODEL 3625 SCREENER SYSTEM
K932948 · Medtronic Vascular · Feb 1994