Cleared Traditional

K880274 - ADVANCED SURGICAL PRODUCTS SCLERAL PLUG...

K880274 is the FDA 510(k) clearance for ADVANCED SURGICAL PRODUCTS SCLERAL PLUG... by Advanced Surgical Products, Inc.. It is a Class 1 Ophthalmic device (product code HNR) cleared through the Traditional 510(k) pathway after a 15-day FDA review.

K880274 · Advanced Surgical Products, Inc. · Ophthalmic device
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Feb 1988
Decision
15d
Days
Class 1
Risk

K880274 is an FDA 510(k) clearance for the ADVANCED SURGICAL PRODUCTS SCLERAL PLUG FORCEPS. Classified as Forceps, Ophthalmic (product code HNR), Class I - General Controls.

Submitted by Advanced Surgical Products, Inc. (Chesterfield, US). The FDA issued a Cleared decision on February 5, 1988 after a review of 15 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.4350 - the FDA ophthalmic 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 Advanced Surgical Products, Inc. devices

Submission Details

510(k) Number K880274 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 21, 1988
Decision Date February 05, 1988
Days to Decision 15 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
95d faster than avg
Panel avg: 110d · This submission: 15d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code HNR Forceps, Ophthalmic
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.4350
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 - HNR Forceps, Ophthalmic

All 28
Devices cleared under the same product code (HNR) and FDA review panel - the closest regulatory comparables to K880274.
ALCON FOLDING FORCEPS
K895434 · Alcon Laboratories · Dec 1989
MCDONALD FOLDING FORCEPS
K885230 · Alcon Laboratories · May 1989
THORTON TITANIUM NEEDLEHOLDERS(NO,W CATCH & STAND
K863991 · Keeler Instruments, Inc. · Oct 1986
THORNTON TITANIUM FORCEPS (VARIOUS TYPES)
K863992 · Keeler Instruments, Inc. · Oct 1986
PACO-FOLDER (TM) INTRAOCULAR LENS FORCEPS
K864003 · Allergan, Inc. · Oct 1986
MANUAL OPHTHALMIC SURGICAL INSTRUMENTS
K861141 · CooperVision, Inc. · Apr 1986