Cleared Traditional

K960969 - GALVA 5-T

K960969 is an FDA 510(k) clearance for GALVA 5-T, manufactured by Zimmer Elektromedizin GmbH. The device is a Class 2 Neurology device with product code GZJ cleared through the Traditional 510(k) pathway after a 65-day FDA review.

K960969 · Zimmer Elektromedizin GmbH · Neurology device
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May 1996
Decision
65d
Days
Class 2
Risk

K960969 is an FDA 510(k) clearance for the GALVA 5-T. Classified as Stimulator, Nerve, Transcutaneous, For Pain Relief (product code GZJ), Class II - Special Controls.

Submitted by Zimmer Elektromedizin GmbH (D7910 Neu-Ulm, DE). The FDA issued a Cleared decision on May 15, 1996 after a review of 65 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.

View all Zimmer Elektromedizin GmbH devices

FDA 510(k) Submission Details - K960969

510(k) Number K960969 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 11, 1996
Decision Date May 15, 1996
Days to Decision 65 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
83d faster than avg
Panel avg: 148d · This submission: 65d
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 276
Devices cleared under the same product code (GZJ) and FDA review panel - the closest regulatory comparables to K960969.
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ACUPLUS
K954334 · S.H.P. Intl. Pty., Ltd. · Jan 1996
PGS123 AND HVS-123
K946299 · Skylark Device Co., Ltd. · Jun 1995