Cleared Traditional

K882422 - DISPOSABLE ARACHNOID KNIFE

K882422 is an FDA 510(k) clearance for DISPOSABLE ARACHNOID KNIFE, manufactured by Microbio-Medics, Inc.. The device is a Class 1 Neurology device with product code HAO cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K882422 · Microbio-Medics, Inc. · Neurology device
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Sep 1988
Decision
85d
Days
Class 1
Risk

K882422 is an FDA 510(k) clearance for the DISPOSABLE ARACHNOID KNIFE. Classified as Instrument, Surgical, Non-powered (product code HAO), Class I - General Controls.

Submitted by Microbio-Medics, Inc. (Columbus, US). The FDA issued a Cleared decision on September 6, 1988 after a review of 85 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.4535 - 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 Microbio-Medics, Inc. devices

FDA 510(k) Submission Details - K882422

510(k) Number K882422 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 13, 1988
Decision Date September 06, 1988
Days to Decision 85 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
63d faster than avg
Panel avg: 148d · This submission: 85d
Pathway characteristics
Predicate-based equivalence.

HAO Device Classification - Class 1, General Controls

Product Code HAO Instrument, Surgical, Non-powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 882.4535
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - HAO Instrument, Surgical, Non-powered

All 24
Devices cleared under the same product code (HAO) and FDA review panel - the closest regulatory comparables to K882422.
AUTO SUTURE SPINAL ELEVATOR
K942970 · United States Surgical, A Division of Tyco Healthc · Jul 1994
AUTO SUTURE SPINAL DISSECTOR
K942971 · United States Surgical, A Division of Tyco Healthc · Jul 1994
TAYLOR SPINAL RETRACTOR
K892546 · Zinnanti Surgical Instruments, Inc. · May 1989
MALLEABLE PTFE COATED BRAIN SPATULAE
K880278 · Downs Surgical , Ltd. · Feb 1988
RANGE OF TITANIUM NEUROSURGERY INSTRUMENTS
K874630 · Downs Surgical , Ltd. · Dec 1987
FUJITSU MALLEABLE - TIP BRAIN SPATULA
K862331 · Downs Surgical , Ltd. · Jul 1986