Cleared Traditional

K851784 - 27-210 PLASTER KNIFE (REINER)

K851784 is an FDA 510(k) clearance for 27-210 PLASTER KNIFE (REINER), manufactured by Artiberia. The device is a Class 1 General & Plastic Surgery device with product code EMF cleared through the Traditional 510(k) pathway after a 56-day FDA review.

K851784 · Artiberia · General & Plastic Surgery device
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Jun 1985
Decision
56d
Days
Class 1
Risk

K851784 is an FDA 510(k) clearance for the 27-210 PLASTER KNIFE (REINER). Classified as Knife, Surgical (product code EMF), Class I - General Controls.

Submitted by Artiberia (San Antonio, US). The FDA issued a Cleared decision on June 20, 1985 after a review of 56 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 Artiberia devices

FDA 510(k) Submission Details - K851784

510(k) Number K851784 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 25, 1985
Decision Date June 20, 1985
Days to Decision 56 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
59d faster than avg
Panel avg: 115d · This submission: 56d
Pathway characteristics
Predicate-based equivalence.

EMF Device Classification - Class 1, General Controls

Product Code EMF Knife, 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 - EMF Knife, Surgical

All 10
Devices cleared under the same product code (EMF) and FDA review panel - the closest regulatory comparables to K851784.
VAN-TEC ENDOPYELOTOMY KNIFE
K880094 · Van-Tec, Inc. · Feb 1988
VALTRAC (BAR) REMOVER DEVICE
K863752 · Davis & Geck, Inc. · Oct 1986
REUSABLE/DISPOSABLE AUTOPSY KNIFE SET
K863549 · Surgipath Medical Industries, Inc. · Sep 1986
VALVOTOMY KNIFE
K843371 · Downs Surgical , Ltd. · Oct 1984
H.R. JAKOBI SURG. INSTRUMENTS #11 38/67
K834184 · Imm Enterprises , Ltd. · Jan 1984
JAKOBI SURG. INSTR- #11 38/39/45/46/67
K834197 · Imm Enterprises , Ltd. · Jan 1984