Cleared Traditional

K841320 - PERCUTANEOUS TRIG. FINGER RELEASE KNIFE

K841320 is an FDA 510(k) clearance for PERCUTANEOUS TRIG. FINGER RELEASE KNIFE, manufactured by Anapach Effort, Inc.. The device is a Class 1 General & Plastic Surgery device with product code GES cleared through the Traditional 510(k) pathway after a 22-day FDA review.

K841320 · Anapach Effort, Inc. · General & Plastic Surgery device
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Apr 1984
Decision
22d
Days
Class 1
Risk

K841320 is an FDA 510(k) clearance for the PERCUTANEOUS TRIG. FINGER RELEASE KNIFE. Classified as Blade, Scalpel (product code GES), Class I - General Controls.

Submitted by Anapach Effort, Inc. (Walker, US). The FDA issued a Cleared decision on April 24, 1984 after a review of 22 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4800 - the FDA general and plastic surgery 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 Anapach Effort, Inc. devices

FDA 510(k) Submission Details - K841320

510(k) Number K841320 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 02, 1984
Decision Date April 24, 1984
Days to Decision 22 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
93d faster than avg
Panel avg: 115d · This submission: 22d
Pathway characteristics
Predicate-based equivalence.

GES Device Classification - Class 1, General Controls

Product Code GES Blade, Scalpel
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4800
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 - GES Blade, Scalpel

All 11
Devices cleared under the same product code (GES) and FDA review panel - the closest regulatory comparables to K841320.
DEXTRA DISPOSABLE BLADES
K863867 · Storz Instrument Co. · Oct 1986
ANGIOMED SKIN FASCIA KNIFE
K855104 · Angiomed U.S., Inc. · Jan 1986
STAINLESS STEEL & CARBON STEEL STERILE BLADES
K853528 · Abco Dealers, Inc. · Sep 1985
FASCIA CUTTER
K834514 · Stryker Corp. · Mar 1984
H.R. JAKOBI SURG. INSTRUMENTS #11 27/37
K834182 · Imm Enterprises , Ltd. · Jan 1984
JAKOBI SURG. INSTRUMENTS #1 19/10/26
K834194 · Imm Enterprises , Ltd. · Jan 1984