Cleared Traditional

K792311 - MEDTRONIC MODEL 7728 NEUROMOD

K792311 is an FDA 510(k) clearance for MEDTRONIC MODEL 7728 NEUROMOD, manufactured by Medtronic Vascular. The device is a Class 2 Neurology device with product code GZJ cleared through the Traditional 510(k) pathway after a 5-day FDA review.

K792311 · Medtronic Vascular · Neurology device
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Nov 1979
Decision
5d
Days
Class 2
Risk

K792311 is an FDA 510(k) clearance for the MEDTRONIC MODEL 7728 NEUROMOD. Classified as Stimulator, Nerve, Transcutaneous, For Pain Relief (product code GZJ), Class II - Special Controls.

Submitted by Medtronic Vascular (Walker, US). The FDA issued a Cleared decision on November 21, 1979 after a review of 5 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.5890 - 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.

FDA 510(k) Submission Details - K792311

510(k) Number K792311 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 16, 1979
Decision Date November 21, 1979
Days to Decision 5 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
144d faster than avg
Panel avg: 149d · This submission: 5d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GZJ Device Classification - Class 2, Special Controls

Product Code GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.5890
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 - GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

All 602
Devices cleared under the same product code (GZJ) and FDA review panel - the closest regulatory comparables to K792311.
THERAPETTE, MODEL NO MH-100
K792473 · Technical Resources, Inc. · Dec 1979
TENS 4500
K792474 · Staodynamics, Inc. · Dec 1979
MODEL 980D TENS NEUROPACER
K792522 · Empi · Dec 1979
NURITE II VRM SINGLE (ELEC. NERVE STIM)
K791833 · Bio-Medical Systems Corp. · Oct 1979
NURITE II VRM DUAL (ELEC. NERVE STIM.)
K791834 · Bio-Medical Systems Corp. · Oct 1979
MODEL 810 VERI/TGS
K791187 · Verite · Aug 1979
K792311 · MEDTRONIC MODEL 7728 NEUROMOD
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