Cleared Traditional

K841247 - SPC DISPOSABLE CUTTER

K841247 is an FDA 510(k) clearance for SPC DISPOSABLE CUTTER, manufactured by Surgical Products Corp.. The device is a Class 1 General & Plastic Surgery device with product code FZT cleared through the Traditional 510(k) pathway after a 42-day FDA review.

K841247 · Surgical Products Corp. · General & Plastic Surgery device
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May 1984
Decision
42d
Days
Class 1
Risk

K841247 is an FDA 510(k) clearance for the SPC DISPOSABLE CUTTER. Classified as Cutter, Surgical (product code FZT), Class I - General Controls.

Submitted by Surgical Products Corp. (Mchenry, US). The FDA issued a Cleared decision on May 2, 1984 after a review of 42 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 Surgical Products Corp. devices

FDA 510(k) Submission Details - K841247

510(k) Number K841247 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 21, 1984
Decision Date May 02, 1984
Days to Decision 42 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
73d faster than avg
Panel avg: 115d · This submission: 42d
Pathway characteristics
Predicate-based equivalence.

FZT Device Classification - Class 1, General Controls

Product Code FZT Cutter, Surgical
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 - FZT Cutter, Surgical

All 35
Devices cleared under the same product code (FZT) and FDA review panel - the closest regulatory comparables to K841247.
SMARTSHEARS
K112400 · Nuscience Consulting and Management Group, LLC · Sep 2011
AUTO SUTURE DISPOSABLE SURGICAL TROCAR*
K890818 · United States Surgical, A Division of Tyco Healthc · May 1989
SCISSORS, VARIOUS
K822448 · J. Sklar Mfg. Co., Inc. · Sep 1982
SURGICAL SCISSORS, SET OF 3
K821632 · Fred Sammons, Inc. · Jun 1982
CONPHAR WIRE CUTTING SCISSORS
K821350 · Conphar, Inc. · May 1982
CONPHAR DISSECTING SCISSORS
K821351 · Conphar, Inc. · May 1982